HRP Conjugation Kit

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  • LYNX Rapid HRP Antibody Conjugation Kit
  • LYNX Rapid HRP Antibody Conjugation Kit
  • LYNX Rapid HRP Antibody Conjugation Kit
  • LYNX Rapid HRP Antibody Conjugation Kit
  • LYNX Rapid HRP Antibody Conjugation Kit
  • LYNX Rapid HRP Antibody Conjugation Kit
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  • Product Type
    Conjugation Kit
1 Formats Available
    Product CodeApplicationsDatasheetMSDSPack SizeList PriceQuantity
    LNK005PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf1 Conjugation For 20mg Antibody
    LNK005P
    LNK001PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf1 Conjugation For 400µg Antibody
    LNK001P
    LNK003PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf1 Conjugation For 4mg Antibody
    LNK003P
    LNK006PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf3 Conjugations For 40µg Antibody
    LNK006P
    LNK002PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf3 Conjugations For 400µg Antibody
    LNK002P
    LNK004PCJdatasheet pdfdatasheet pdf datasheet pdf datasheet pdf5 Conjugations For 4mg Antibody
    LNK004P
    Summary
    Secondary Antibodies
    Negative Isotype Controls
    Useful Reagents
    Positive Controls
    Histology Controls
    More Images
    References
    Reviews
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    • LYNX Rapid HRP Antibody Conjugation Kit® enables the rapid conjugation of a pre-prepared lyophilized mixture containing Horseradish peroxidase (HRP) label to an antibody or protein. Activation of proprietary reagents within the antibody-label solution results in directional covalent bonding of HRP to the antibody.

      The LYNX Rapid Conjugation kit® can be used to label small quantities of antibody/protein at near neutral pH, allowing a high conjugation efficiency with 100% antibody recovery.
    • Intended Use
    • Product Form
    • Reconstitution
    • Preparation
    • Preservative Stabilisers
    • Purity
    • Approx. Protein Concentrations
    • Reagents In The Kit
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 400µg Antibody1 Vial of 100μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 400µg Antibody3 Vials of 100ug LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 4mg Antibody1 Vial of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 5 Conjugations For 4mg Antibody5 Vials of 1mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 1 Conjugation For 20mg Antibody1 Vial of 5mg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
      Pack Size: 3 Conjugations For 40µg Antibody3 Vials of 10μg LYNX lyophilized HRP mix
      1 Vial LYNX Modifier reagent
      1 Vial LYNX Quencher reagent
    • Preparing The Antibody
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100μg HRP you need to add between 100-400μg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 400µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 100µg HRP you need to add between 100-400µg of antibody. For optimal results the antibody volume should be up to 100μl, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 1mg HRP you need to add between 1-4mg of antibody.. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 5 Conjugations For 4mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 4mg HRP you need to add between 1-4mg of antibody. For optimal results the antibody volume should be up to 1ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 1 Conjugation For 20mg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 5mg HRP you need to add between 5-20mg of antibody. For optimal results the antibody volume should be up to 5ml, at a concentration range of 0.5-5.0mg/ml.
      Pack Size: 3 Conjugations For 40µg AntibodyThe following buffer solutions are recommended for preparing the antibody:

      10-50mM amine-free buffer (e.g HEPES, MES, MOPS and phosphate) pH range 6.5-8.5, although moderate concentrations of Tris buffer (<20mM) may be tolerated.

      If possible, avoid buffers containing nucleophilic components such as primary amines and thiols (e.g. thiomersal/thimerosal) since they may react with LYNX chemicals. EDTA and common non-buffering salts and sugars have little or no effect on conjugation efficiency.

      Sodium azide is an irreversible inhibitor of HRP and therefore should be avoided.

      The amount of antibody used for labeling ideally should correspond to molar ratios between 1:4 and 1:1 Ab to HRP. Taking account of the molecular weights (160,000 versus 40,000), this means for that for 10µg HRP you need to add between 10-40µg of antibody. For optimal results the antibody volume should be up to 10μl, at a concentration range of 0.5-5.0mg/ml.
    • Test Principle
    • Buffer Solution
    • Storage
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
      Store kit at -20oC only.
      Newly-conjugated antibody can be stored at 4oC. For long term storage however, the addition of a preservative is recommended, although sodium azide should be avoided.
      Storage in frost-free freezers is not recommended.
      This product should be stored undiluted.
      Avoid repeated freezing and thawing.
    • Shelf Life
      12 months after despatch
      12 months after despatch
      12 months after despatch
      12 months after despatch
      12 months after despatch
      12 months after despatch
    • Acknowledgements
    • Licensed Use
      These products and the methodology of conjugation are patent protected under United Kingdom patent number 2446088 and associated international patent applications. The purchase of this product conveys to the buyer the limited, non exclusive non-transferable right (without the right to resell repackage or further sublicense) under these patents to use the product to make conjugates for research and development purposes only. The purchaser cannot sell or otherwise transfer this product, or its components, or materials or data made using this product, or its components to a third party. Further information on purchasing licenses for diagnostic and other uses may be obtained by contacting Bio-Rad, at. Endeavour House, Langford Business Park, Langford Lane, Kidlington, Oxon. OX5 1GE UNITED KINGDOM. Tel: +44 1865 852 700. E-mail: antibodies@bio-rad.com
    • Regulatory
      For research purposes only
    • This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit the antibody protocols page.

    • Application NameYesNoMin DilutionMax Dilution
      Conjugation
    • Application NameYesNoMin DilutionMax Dilution
      Conjugation
    • Application NameYesNoMin DilutionMax Dilution
      Conjugation
    • Application NameYesNoMin DilutionMax Dilution
      Conjugation
    • Application NameYesNoMin DilutionMax Dilution
      Conjugation
    • Application NameYesNoMin DilutionMax Dilution
      Conjugation


    • We recommend that for each conjugation the user determines the best antibody:conjugate ratio.
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Instructions For Use
      1. To the antibody sample add 1μl of the Modifier reagent for every 10μl of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25°C) for 3 hours, or overnight if preferred.

      4. After incubation, add 1μl of Quencher reagent for every 10μl of antibody used. Leave to stand for 30 minutes before use.

    • Instructions For Use
      1. To the antibody sample add 1μl of the Modifier reagent for every 10ul of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25oC) for 3 hours, or overnight if preferred.

      4. After incubation, add 1μl of Quencher reagent for every 10μl of antibody used. Leave to stand for 30 minutes before use.

    • Instructions For Use
      1. To the antibody sample add 1μl of the Modifier reagent for every 10μl of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25oC) for 3 hours, or overnight if preferred.

      4. After incubation, add 1μl of Quencher reagent for every 10μl of antibody used. Leave to stand for 30 minutes before use.

    • Instructions For Use
      1. To the antibody sample add 1μl of the Modifier reagent for every 10μl of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25oC) for 3 hours, or overnight if preferred.

      4. After incubation, add 1μl of Quencher reagent for every 10μl of antibody used. Leave to stand for 30 minutes before use.

    • Instructions For Use
      1. To the antibody sample add 1ul of the Modifier reagent for every 10ul of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25oC) for 3 hours, or overnight if preferred.

      4. After incubation, add 1ul of Quencher reagent for every 10ul of antibody used. Leave to stand for 30 minutes before use.

    • Instructions For Use
      1. To the antibody sample add 1μl of the Modifier reagent for every 10μl of antibody and mix gently.

      2. Pipette the mixed antibody-modifier sample directly onto the LYNX lyophilized mix and gently pipette up and down twice to resuspend.

      3. Replace cap onto vial and incubate at room temperature (20-25oC) for 3 hours, or overnight if preferred.

      4. After incubation, add 1μl of Quencher reagent for every 10μl of antibody used. Leave to stand for 30 minutes before use.

    Additional HRP Conjugation Kit Formats

    Formats Applications Sizes available
    HRP Conjugation Kit : Kit CJ 1 Conjugation For 4mg Antibody | 1 Conjugation For 20mg Antibody | 1 Conjugation For 400µg Antibody | 3 Conjugations For 400µg Antibody | 3 Conjugations For 40µg Antibody | 5 Conjugations For 4mg Antibody
    • Copyright © 2016 Bio-Rad Antibodies (formerly AbD Serotec)

    Recommended Secondary Antibody

      Recommended Negative Isotype Control

        Useful Reagents

          Recommended Positive Controls

            Histology Controls

              References

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