CD2 Antibody | OX-34

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CD2 Antibody | OX-34 gallery image 1

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
Ey and Toy are redundantly required to activate stg-FMW. (A) The pattern of conservation of stg-FMW enhancer sequence in Drosophila species as displayed by the UCSC genome browser (http://genome.ucsc.edu) is shown at the top. Two highly conserved regions harboring binding sites for Pax6, BS1 and BS2, and Hth are shown below. (B) Logo of the optimized PAX6 Position Weight Matrix (PWM) used in this study. Nucleotide preference is represented by the height of the letter. (C) Partial sequence of BS1 and BS2. BS1 contains binding sites for So and Pax6 genes (Ey/Toy) highlighted in blue and red, respectively. BS1*: Mutated version of BS1. Ey/Pax6 mutated bases are shown in lowercase. BS2 contains adjacent binding sites for Pax6 (Ey/Toy) and Hth, highlighted in red and green respectively. Mutated core bases for Pax6 (Ey/Toy) and Hth are shown in lowercase in BS2*. (D—G) Analysis of the expression of stg-FMW upon mutation of BS1 or BS2. Representative L3 eye imaginal discs carrying the wild type stg-FMW (D), and the mutated versions stg*BS1 (E) and stg*BS2 (F) of the enhancer. (G) Expression of GFP is not affected upon mutation of BS1 or BS2 in stg-FMW. Simultaneous mutation of BS1 and BS2 (stg*BS1+*BS2) abolishes GFP expression in the eye field; small GFP dots can be detected but only at the dorsal and ventral margins of the eye disc. Discs are outlined by the white dashed lines. The position of the MF is indicated by the white arrow and yellow dashed line. (H—J) Clones of ey (H) or toy (I) RNAi, in the eye imaginal disc. Clones are outlined and marked by the absence of CD2 (red). Expression of stg-FMW (green) is not affected by downregulation of Ey or Toy. (J) Eye disc containing ey and toy double mutant clones, stained for CD2 (red) and stg-FMW (green). In clones of cells double mutant for ey and toy the expression of stg-FMW is lost. White arrow indicates the position of the MF. In all images anterior is to the left.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 2

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
So/Eya are positive regulators of stg-FMW. (A) Eye imaginal disc with clones of cells mutant for eya, labeled by the absence of CD2 (red). (A’) Within the clone cells, stg-FMW expression (green) is not activated. (A”) Hth expression (blue) is maintained in eya RNAi cells. (B) MARCM eya-hth- clones (GFP) stained for stg-FMW (lacZ- red) (B’) and Hth (B”)(blue), showing that eya is required for stg-FMW expression. Clones are outlined. The asterisk (*) in A indicates the normal expression pattern of Hth, during L3, in pigment progenitor cells posterior to the MF [17]. In all images anterior is to the left.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 3

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
Hth defines the anterior domain of stg-FMW expression. (A) Clone of cells ectopically expressing Hth-HA, labeled in magenta, and stained for stg-FMW (green). (A’) Expression of stg-FMW is only repressed within the anterior domain of the clone. (B) Eye disc containing clones of a null allele of hth (hthP2), stained for CD2 (red) and stg-FMW (green). Clone cells are labeled by the absence of CD2. Within the clone stg-FMW expression occurs in a few cell rows anterior to its normal domain of expression. Arrow indicates premature expression of GFP. The vertical dashed line limits the most anterior expression of stg-FMW in wild-type tissue. The horizontal line represents the width of stg-FWW expression in wild-type tissue. (C) Mutation of the Hth BS (stg*Hth) does not affect the spatial or temporal expression of stg-FMW.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 4

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
Hth defines the anterior domain of stg-FMW expression. (A) Clone of cells ectopically expressing Hth-HA, labeled in magenta, and stained for stg-FMW (green). (A’) Expression of stg-FMW is only repressed within the anterior domain of the clone. (B) Eye disc containing clones of a null allele of hth (hthP2), stained for CD2 (red) and stg-FMW (green). Clone cells are labeled by the absence of CD2. Within the clone stg-FMW expression occurs in a few cell rows anterior to its normal domain of expression. Arrow indicates premature expression of GFP. The vertical dashed line limits the most anterior expression of stg-FMW in wild-type tissue. The horizontal line represents the width of stg-FWW expression in wild-type tissue. (C) Mutation of the Hth BS (stg*Hth) does not affect the spatial or temporal expression of stg-FMW.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 5

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
Expression of stg mRNA is not affected in ey2 mutants. (A—E) In situ hybridization of stg mRNA on ey2 homozygous discs shows that the levels and expression pattern of stg are not significantly affected, despite the growth defect and abnormal MF progression. The solid white line depicts the MF in ey2 and the white dashed line represents the position where the MF should be if progression was uniform in dorsal and ventral domains. (B, C) Higher magnification images of the discs in (A). Representative ey2 eye imaginal discs are shown. (F-G) The activity of stg-FMW enhancer is not affected upon ey mutation. Eye-antennal imaginal discs mutant for ey2 showing expression of GFP driven by stg-FMW. GFP expression (green) is not affected despite the evident irregular progression of the MF. Eya is shown in red. (H-K) One Pax6 BS suffices for enhancer activity. Eye imaginal discs containing clones of ey RNAi (H, I) and toy RNAi (J, K) in the presence of either stg-BS1* or stg-BS2* mutant stg-FMW enhancer. Clones are marked by the absence of CD2 (red) and outlined. GFP expression driven by either stg-BS1* or stg-BS2* is shown in green. In none of these combinations, GFP expression is affected, indicating that Ey and Toy do not show functional preference for either BS1 or BS2.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 6

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 fusion proteins inDrosophila by immunofluorescence.
Image caption:
Activation of the Dpp or the Hh pathway does not lead to precocious activation of stg-FMW. Clones of gain of function of an activated form of thickveins (tkvQD) (A-C) and Cubitus interruptus (ci) (D) showing that the Dpp and Hh signalling pathways do not suffice for activation of stg-FMW in other domains of the eye imaginal disc. Clones are labelled by the absence of CD2 (magenta). The activity of stg-FMW is detected by the expression of GFP (green). Clones are outlined. Anterior is to the left.

From: Lopes CS, Casares F (2015) Eye Selector Logic for a Coordinated Cell Cycle Exit. PLoS Genet 11(2): e1004981.

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CD2 Antibody | OX-34 gallery image 7

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 tagged fusion protein in Drosophila by immunofluorescence.
Image caption:
Protrusion formation during mesoderm flattening. (A,B) Two-photon time-lapse sequence of mesoderm cells expressing GFP-Actin in the period following EMT (ventral imaging protocol; see Fig. S1 in the supplementary material). VM, ventral midline; DL, dorsolateral ectoderm. (A) Intensity-rendered 3D reconstructions (see Movie 4 in the supplementary material); (B) transverse sections (see Movie 5 in the supplementary material). Cells at the dorsal edge (DECs) protrude radially (white arrows) and move towards the ectoderm (yellow arrows indicate ventral cells protruding into the ectoderm). (C) DEC (white arrows) and more ventral cell (yellow arrows) protrusions visualised in a wild-type twi::CD2-expressing embryo fixed during mesoderm flattening (3D reconstructed image shown rotating in Movie 6 in the supplementary material). Embryo in C is shown in ventrolateral view, anterior towards the left.

From: Clark IB, Muha V, Klingseisen A, Leptin M, Müller HA. Fibroblast growth factor signalling controls successive cell behaviours during mesoderm layer formation in Drosophila. Development. 2011 Jul;138(13):2705-15.

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CD2 Antibody | OX-34 gallery image 8

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 tagged fusion protein in Drosophila by immunofluorescence.
Image caption:
Protrusion formation during mesoderm flattening. (A,B) Two-photon time-lapse sequence of mesoderm cells expressing GFP-Actin in the period following EMT (ventral imaging protocol; see Fig. S1 in the supplementary material). VM, ventral midline; DL, dorsolateral ectoderm. (A) Intensity-rendered 3D reconstructions (see Movie 4 in the supplementary material); (B) transverse sections (see Movie 5 in the supplementary material). Cells at the dorsal edge (DECs) protrude radially (white arrows) and move towards the ectoderm (yellow arrows indicate ventral cells protruding into the ectoderm). (C) DEC (white arrows) and more ventral cell (yellow arrows) protrusions visualised in a wild-type twi::CD2-expressing embryo fixed during mesoderm flattening (3D reconstructed image shown rotating in Movie 6 in the supplementary material). Embryo in C is shown in ventrolateral view, anterior towards the left.

From: Clark IB, Muha V, Klingseisen A, Leptin M, Müller HA. Fibroblast growth factor signalling controls successive cell behaviours during mesoderm layer formation in Drosophila. Development. 2011 Jul;138(13):2705-15.

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CD2 Antibody | OX-34 gallery image 9

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 tagged fusion protein in Drosophila by immunofluorescence.
Image caption:
A role for Cdc42 at the mesoderm/ectoderm interface. (A) Comparison of dorsal and radial protrusions (from twi::CD2 stainings) in wild-type embryos (yellow bars) and embryos expressing UAS::Cdc[N17] driven by twi::Gal4. The asterisks indicate statistically significant differences in the number of radial protrusions [P<0.05 (n=5); two-sample t-test]. There is no difference in the number of dorsal protrusions [P>0.05 (n=5); two-sample t-test]. Data are mean±s.d. (B) Wild-type and Cdc42 mutant embryos (obtained from Cdc424/Cdc426 trans-heterozygous females) were stained for Twi (stages 8-10) and for Eve (stage 12). Note irregular distribution of mesoderm nuclei in Cdc42 mutants compared with wild type, indicating defects in mesoderm spreading. Arrowheads in stage 12 embryos indicate position of segmental Eve-positive dorsal mesoderm cells; note the strong reduction in the number of Eve-positive hemi-segments. (C) E-cadherin immunostaining of embryos (stage 9) expressing UAS::Cdc[N17] driven by twi::Gal4 compared with wild type. E-cadherin accumulates at the ectoderm-mesoderm interface (mesoderm is marked in red with CD2), which is absent in embryos expressing dominant-negative Cdc42.

From: Clark IB, Muha V, Klingseisen A, Leptin M, Müller HA. Fibroblast growth factor signalling controls successive cell behaviours during mesoderm layer formation in Drosophila. Development. 2011 Jul;138(13):2705-15.

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CD2 Antibody | OX-34 gallery image 10

Published customer image:
Mouse anti Rat CD2 antibody, clone OX-34 used for the detection of rat CD2 tagged fusion protein in Drosophila by immunofluorescence.
Image caption:
Recruitment of presumptive notal cells to the wing fate by ectopic Wg- and Vg-expressing cells. (A-B') Wild-type Drosophila discs containing Tuba1>Gal4/UAS-vg UAS-wg clones located within the presumptive notum, probed for Vg (A, red), 5XQE-DsRed (B, red) and rn-lacZ (B', blue) expression and marked by Vg overexpression (A, bright red) or loss of GFP (B). Arrows indicate clones that have induced `ectopic' wing pouches; note that rn-lacZ expression (B') extends beyond that of 5XQE-DsRed (B), as in the normal pouch. (C-F) Discs that express UAS-vg in A compartment border cells under dpp-Gal4 control [red by ectopic 1XQE-lacZ (D) and Vg (E,F) expression] and contain P compartment clones of Tuba1>Nrt-wg cells (indicated by the arrow in C; black by the absence of CD2, green. The arrowed clone in F is shown at higher magnification in E,E'. Cells within the clones that are located within 10-20 cell diameters of the A-P boundary ectopically express normal peak levels of 1XQE-lacZ (D) and endogenous Vg (E') and induce immediately adjacent cells across the clone border to do the same (appear yellow in overlap with CD2). (G-H') UAS>Nrt-wg (G,G') or UAS>arm* (H,H') clones (marked green by Flu epitope staining of Nrt-Wg and Arm*) located within the presumptive notum ectopically express normal peak levels of endogenous Vg (dull red) when they abut UAS>vg clones (bright red by Vg overexpression) and are located within 10-20 cell diameters of the A-P boundary. The UAS>Nrt-wg clones, but not the UAS>arm* clones, also induce their immediate neighbors to do the same.

From: Zecca M, Struhl G. Recruitment of cells into the Drosophila wing primordium by a feed-forward circuit of vestigial autoregulation. Development. 2007 Aug;134(16):3001-10.

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  • Mouse anti Rat CD2
  • Mouse anti Rat CD2:Alexa Fluor® 647
  • Mouse anti Rat CD2:Alexa Fluor® 488
  • Mouse anti Rat CD2
  • Mouse anti Rat CD2
  • Mouse anti Rat CD2:RPE
(Rated 0.0 out of 5 based on 0 customer reviews)
  • Product Type
    Monoclonal Antibody
  • Clone
    OX-34
  • Isotype
    IgG2a
4 Formats Available
    Product CodeApplicationsDatasheetMSDSPack SizeList PriceQuantity
    MCA154GAC, F, IF, IP, P *datasheet pdfdatasheet pdf0.1 mg
    MCA154GA
    MCA154RC, F, IF, IP, P *datasheet pdfdatasheet pdf0.25 mg
    MCA154R
    MCA154GC, F, IF, IP, P *datasheet pdfdatasheet pdf1 mg
    MCA154G
    MCA154PEFdatasheet pdfdatasheet pdf100 Tests
    MCA154PE
    MCA154A647Fdatasheet pdfdatasheet pdf100 Tests/1ml
    MCA154A647
    MCA154A488Fdatasheet pdfdatasheet pdf100 Tests/1ml
    MCA154A488
    Summary
    Secondary Antibodies
    Negative Isotype Controls
    Useful Reagents
    Positive Controls
    Histology Controls
    More Images
    References
    Reviews
    -
    • Mouse anti Rat CD2 antibody, clone OX-34 recognizes a determinant on thymocytes and peripheral T-cells but it does not bind to B cells or peritoneal macrophages. The antigen recognized by this antibody is a 50-54 kDa glycoprotein, homolog of the human CD2 antigen (Williams et al. 1987).
    • Intended Use
    • Target Species
      Rat
    • Product Form
      Purified IgG - liquid
      Purified IgG conjugated to Alexa Fluor® 647 - liquid
      Purified IgG conjugated to Alexa Fluor® 488 - liquid
      Purified IgG - liquid
      Purified IgG - liquid
      Purified IgG conjugated to R. Phycoerythrin (RPE) - lyophilised
    • Reconstitution
      Reconstitute with 1ml distilled water
    • Preparation
      Purified IgG prepared by affinity chromatography on Protein G
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G
      Purified IgG prepared by affinity chromatography on Protein G
      Purified IgG prepared by affinity chromatography on Protein G
    • Preservative Stabilisers
      0.09%Sodium Azide
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      0.09%Sodium Azide
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      5%Sucrose
    • Immunogen
      Activated rat T helper cells.
    • Purity
    • Approx. Protein Concentrations
      IgG concentration 1.0 mg/ml
      IgG concentration 0.05 mg/ml
      IgG concentration 0.05 mg/ml
      IgG concentration 1.0 mg/ml
      IgG concentration 1.0 mg/ml
    • Reagents In The Kit
    • Preparing The Antibody
    • Test Principle
    • Buffer Solution
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
    • Fusion Partners
      Spleen cells from immunised BALB/c mice were fused with cells of the NS1 mouse myeloma cell line.
    • Storage
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Prior to reconstitution store at +4oC. Following reconstitution store at +4oC.

      DO NOT FREEZE.

      This product should be stored undiluted. This product is photosensitive and should be protected from light. Should this product contain a precipitate we recommend microcentrifugation before use.
    • Shelf Life
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      12 months from date of reconstitution.
    • GO Terms
      extracellular space
      protein kinase binding
      antigen binding
      fully spanning the plasma membrane
      receptor tyrosine kinase binding
      protein complex
      cell-cell adhesion
      protein self-association
      protein homodimerization activity
      integral to membrane
      membrane raft
      T cell activation
      glycoprotein binding
      cell surface
    • UniProt
    • Entrez Gene
    • Acknowledgements
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.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
      Flow Cytometry1/50
      Immunofluorescence
      Immunohistology - Frozen
      Immunoprecipitation
      Immunohistology - Paraffin(1)
      (1)
      We recommend the use of PLP fixation for optimal results, see Whiteland et al.
    • Application NameYesNoMin DilutionMax Dilution
      Flow CytometryNeat1/10
    • Application NameYesNoMin DilutionMax Dilution
      Flow CytometryNeat1/10
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry1/50
      Immunofluorescence
      Immunohistology - Frozen
      Immunoprecipitation
      Immunohistology - Paraffin(1)
      (1)
      We recommend the use of PLP fixation for optimal results, see Whiteland et al.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry1/50
      Immunofluorescence
      Immunohistology - Frozen
      Immunoprecipitation
      Immunohistology - Paraffin(1)
      (1)
      We recommend the use of PLP fixation for optimal results, see Whiteland et al.
    • Application NameYesNoMin DilutionMax Dilution
      Flow CytometryNeat

    • Where this antibody has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the antibody for use in their own system using appropriate negative/positive controls.
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Flow Cytometry
      Use 10ul of the suggested working dilution to label 106 cells in 100ul.
    • 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
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use

    Additional CD2 Antibody Formats

    Formats Clone Applications Sizes available
    CD2 Antibody : Purified OX-34 C, F, IF, IP, P * 1 mg | 0.1 mg | 0.25 mg
    CD2 Antibody : Alexa Fluor® 488 OX-34 F 100 Tests/1ml
    CD2 Antibody : Alexa Fluor® 647 OX-34 F 100 Tests/1ml
    CD2 Antibody : RPE OX-34 F 100 Tests
    • Copyright © 2016 Bio-Rad

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      Goat anti Mouse IgG (H/L):FITC (Multi Species Adsorbed)STAR117F0.5 mgF
      STAR117F
      Goat anti Mouse IgG:FITC (Rat Adsorbed)STAR700.5 mgF
      STAR70
      Goat anti Mouse IgG (Fc):FITCSTAR120F1 mgC, F
      STAR120F
      Rabbit F(ab')2 anti Mouse IgG:FITCSTAR9B1 mgF
      STAR9B
      Human anti Mouse IgG2a:HRPHCA037P0.1 mgE
      HCA037P
      Goat anti Mouse IgG (H/L):HRP (Multi Species Adsorbed)STAR117P0.5 mgE, WB
      STAR117P
      Goat anti Mouse IgG:HRP (Rat Adsorbed)STAR770.5 mgC, E, P
      STAR77
      Goat anti Mouse IgG (Fc):HRPSTAR120P1 mgE, WB
      STAR120P
      Rabbit F(ab')2 anti Mouse IgG:HRP (Human Adsorbed)STAR13B1 mgC, E, P, RE, WB
      STAR13B
      Goat anti Mouse IgG/A/M:HRP (Human Adsorbed)STAR87P1 mgE
      STAR87P
      Rabbit F(ab')2 anti Mouse IgG:RPESTAR12A1 mlF
      STAR12A
      Goat anti Mouse IgG:RPE (Rat Adsorbed)STAR761 mlF
      STAR76
      DescriptionProduct CodePack SizeApplicationsList PriceQuantity
      Goat anti Mouse IgG (H/L):Alk. Phos. (Multi Species Adsorbed)STAR117A0.5 mgE, WB
      STAR117A
      Goat anti Mouse IgG/A/M:Alk. Phos.STAR87A1 mgC, E, WB
      STAR87A
      Goat anti Mouse IgG (H/L):DyLight®488 (Multi Species Adsorbed)STAR117D488GA0.1 mgF, IF
      STAR117D488GA
      Goat anti Mouse IgG (H/L):DyLight®549 (Multi Species Adsorbed)STAR117D549GA0.1 mgF, IF
      STAR117D549GA
      Goat anti Mouse IgG (H/L):DyLight®649 (Multi Species Adsorbed)STAR117D649GA0.1 mgF, IF
      STAR117D649GA
      Goat anti Mouse IgG (H/L):DyLight®680 (Multi Species Adsorbed)STAR117D680GA0.1 mgF, WB
      STAR117D680GA
      Goat anti Mouse IgG (H/L):DyLight®800 (Multi Species Adsorbed)STAR117D800GA0.1 mgF, IF, WB
      STAR117D800GA
      Rabbit F(ab')2 anti Mouse IgG:Dylight®800STAR8D800GA0.1 mgF, IF, WB
      STAR8D800GA
      Human anti Mouse IgG2a:FITCHCA037F0.1 mgF
      HCA037F
      Goat anti Mouse IgG (H/L):FITC (Multi Species Adsorbed)STAR117F0.5 mgF
      STAR117F
      Goat anti Mouse IgG:FITC (Rat Adsorbed)STAR700.5 mgF
      STAR70
      Goat anti Mouse IgG (Fc):FITCSTAR120F1 mgC, F
      STAR120F
      Rabbit F(ab')2 anti Mouse IgG:FITCSTAR9B1 mgF
      STAR9B
      Human anti Mouse IgG2a:HRPHCA037P0.1 mgE
      HCA037P
      Goat anti Mouse IgG (H/L):HRP (Multi Species Adsorbed)STAR117P0.5 mgE, WB
      STAR117P
      Goat anti Mouse IgG:HRP (Rat Adsorbed)STAR770.5 mgC, E, P
      STAR77
      Goat anti Mouse IgG (Fc):HRPSTAR120P1 mgE, WB
      STAR120P
      Rabbit F(ab')2 anti Mouse IgG:HRP (Human Adsorbed)STAR13B1 mgC, E, P, RE, WB
      STAR13B
      Goat anti Mouse IgG/A/M:HRP (Human Adsorbed)STAR87P1 mgE
      STAR87P
      Rabbit F(ab')2 anti Mouse IgG:RPESTAR12A1 mlF
      STAR12A
      Goat anti Mouse IgG:RPE (Rat Adsorbed)STAR761 mlF
      STAR76

      Recommended Negative Isotype Control

        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative ControlMCA1210100 TestsF
        MCA1210
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative Control:Alexa Fluor® 647MCA1210A647100 Tests/1mlF
        MCA1210A647
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative Control:Alexa Fluor® 488MCA1210A488100 Tests/1mlF
        MCA1210A488
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative ControlMCA1210100 TestsF
        MCA1210
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative ControlMCA1210100 TestsF
        MCA1210
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Mouse IgG2a Negative Control:RPEMCA1210PE100 TestsF
        MCA1210PE

        Useful Reagents

          Recommended Positive Controls

            Histology Controls

              References

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