READILINK™





READILINK™ 680/701 Antibody Labeling Kit
READILINK™ 405/454 Antibody Labeling Kit
READILINK™ 405/508 Antibody Labeling Kit
READILINK™ 405/537 Antibody Labeling Kit
READILINK™ 492/516 Antibody Labeling Kit
READILINK™ 555/570 Antibody Labeling Kit
READILINK™ 594/610 Antibody Labeling Kit
READILINK™ 633/655 Antibody Labeling Kit
READILINK™ 647/674 Antibody Labeling Kit
READILINK™ 700/713 Antibody Labeling Kit
READILINK™ 750/780 Antibody Labeling Kit
READILINK™ 790/811 Antibody Labeling Kit
- Product Type
- Conjugation Kit
Product Code | Applications | Pack Size | List Price | Quantity |
---|---|---|---|---|
1351007 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351011 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351012 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351013 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351002 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351003 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351004 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351005 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351006 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351008 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351009 | CJ | 2 Conjugations For 50 µg Antibody | ||
1351010 | CJ | 2 Conjugations For 50 µg Antibody |
The ReadiLink Antibody Labeling Kit provides all the essential components for performing two conjugation reactions (2 x 50 µg). Each kit can be used to label monoclonal or polyclonal antibodies or other proteins (>10 kDa).
Product Details
- Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer - Reagents in the Kit
- 2 vials ReadiLink Labeling Dye (powder) (Note: Use one vial to label 50 μg of antibodies)
1 vial (20 μl) Reaction Buffer
1 vial (20 μl) Quench Buffer
Storage Information
- Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Storage
- Store at -20oC only.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. - Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Please see label for expiry date.
- Guarantee
- Please see label for expiry date.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
- Guarantee
- Guaranteed until date of expiry. Please see product label.
More Information
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Acknowledgements
- ReadiLink™ is a trademark of AAT Bioquest, Inc.
- Regulatory
- For research purposes only
Applications of READILINK™
Application Name | Verified | Min Dilution | Max Dilution |
---|---|---|---|
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation | |||
Conjugation |
- Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use. - Instructions For Use
- Important: Thaw all kit components prior to use.
Note: The antibody of interest must be suspended in phosphate buffered saline (PBS), pH 7.2-7.4, or be dialyzed against PBS prior to conjugation to remove free amines or ammonium salts in the solution.
Note: The optimal antibody conjugation is 1 mg/ml. A conjugation performed at a different conjugation concentration may cause suboptimal labeling.
1. Suspend the antibody of interest in PBS to create a 1 mg/ml concentration.
2. Add 5 μl reaction buffer to 50 μl antibody solution from step 1.
3. Mix well by pipetting up and down a few times.
4. Add the entire volume (55 μl) to one vial of labeling dye and mix by pipetting.
5. Incubate for 60 min at room temperature.
6. Add 5 μl quencher to the reaction mixture.
7. Incubate for 10 min at room temperature.
Antibodies are now labeled and ready to use.
Fluorescent Spectraviewer
Watch the Tool Tutorial Video ▸
How to Use the Spectraviewer?
Watch the Tool Tutorial Video ▸
- Start by selecting the application you are interested in, with the option to select an instrument from the drop down menu or create a customized instrument
- Select the fluorophores or fluorescent proteins you want to include in your panel to check compatibility
- Select the lasers and filters you wish to include
- Select combined or multi-laser view to visualize the spectra