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APC anti-mouse CD152 Antibody

Pricing & Availability
Clone
UC10-4B9 (See other available formats)
Regulatory Status
RUO
Other Names
Cytotoxic T Lymphocyte-Associated Antigen-4 (CTLA-4), Ly-56
Isotype
Armenian Hamster IgG
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Product Citations
publications
A_UC10-4B9_APC_100809
Con A+IL-2-stimulated C57BL/6 splenocytes (3 days) stained with UC10-4B9 APC and CD3e (145-2C11) PE
  • A_UC10-4B9_APC_100809
    Con A+IL-2-stimulated C57BL/6 splenocytes (3 days) stained with UC10-4B9 APC and CD3e (145-2C11) PE
  • B_UC10-4B9_APC_100809
    Con A+IL-2-stimulated C57BL/6 splenocytes (3 days) stained with Armenian Hamster IgG isotype APC and CD3e (145-2C11) PE
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106309 25 µg 91€
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106310 100 µg 247€
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Description

CD152, also known as CTLA-4 or Ly-56, is a 33 kD member of the immunoglobulin superfamily. It is expressed on activated T and B lymphocytes. CD152 is similar to CD28 in amino acid sequence, structure, and genomic organization and these two receptors share common B7 family counter-receptors (B7-1, B7-2). Whereas CD28 delivers a costimulatory signal in T cell activation, CTLA-4 negatively regulates cell-mediated immune responses. CD152 is thought to play a role in the induction and maintenance of immunological tolerance as well as the development of protective immunity and thymocyte regulation.

Product Details
Technical data sheet

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Armenian Hamster
Immunogen
Mouse CTLA-4-mouse IgG2a fusion protein
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with APC under optimal conditions.
Concentration
0.2 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

FC - Quality tested
Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is ≤1.0 µg per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.

Excitation Laser
Red Laser (633 nm)
Application Notes

The UC10-4B9 antibody can enhance T cell co-stimulation by blocking CTLA-4 interactions with the B7 co-receptors, favoring CD28 interactions. Additional reported applications (for the relevant formats) include: immunoprecipitation1, in vitro stimulation, in vitro and in vivo blocking1-4 of ligand binding, and as ELISA capture antibody5. To reduce non-specific binding to cells bearing Fc-receptors, pre-incubation of cells with anti-mouse CD16/CD32, clone 93 (Cat. No. 101301/101302), is recommended prior to immunofluorescent staining. For most successful immunofluorescent staining results, it may be important to maximize signal over background by using a relatively bright fluorochrome-antibody conjugate (Cat. No. 106306) or by using a high sensitivity, three-layer staining technique (e.g., including a biotinylated anti-Armenian hamster IgG (Cat. No. 405501) second step, followed by SAv-PE (Cat. No. 405204)). The Ultra LEAF™ purified antibody (Endotoxin < 0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. No. 106327).

Application References

(PubMed link indicates BioLegend citation)
  1. Walunas TL, et al. 1994. Immunity 1:405. (Block, IP)
  2. Cilio CM, et al. 1998. J. Exp. Med. 188:1239. (Block)
  3. Issazadeh S, et al. 1999. J. Immunol. 162:761. (Block)
  4. McCoy K, et al. 1997. J. Exp. Med. 186:183. (Block)
  5. Hsu HC, et al. 2007. J. Immunol. 178:5357. (ELISA Capture)
  6. Sugita S, et al. 2010. Invest. Ophthalmol. Vis. Sci. 51:5783. PubMed
Product Citations
  1. Lehmkuhl P, et al. 2021. Cell Mol Immunol. 18:1677. PubMed
  2. Yang H, et al. 2023. Cell Death Differ. 30:560. PubMed
  3. Zhang P, et al. 2017. Int J Biol Macromol. 10.1016/j.ijbiomac.2017.06.023. PubMed
  4. Schmitt E, et al. 2013. J Immunol. 191:5640. PubMed
  5. Hayatsu N et al. 2017. Immunity. 47(2):268-283 . PubMed
  6. Lu SX, et al. 2021. Cell. . PubMed
  7. Gubser C, et al. 2016. Sci Rep. 6: 25758. PubMed
  8. Sidwell T, et al. 2020. Nat Commun. 0.633333333. PubMed
  9. Emmerson A, et al. 2018. J Clin Invest. 128:3088. PubMed
  10. Wong HS, et al. 2021. Cell. . PubMed
  11. Espinosa JR, et al. 2018. Front Immunol. 9:1371. PubMed
  12. Yue X, et al. 2019. Nat Commun. 10:2011. PubMed
  13. Harb H, et al. 2021. Immunity. 54(6):1186-1199.e7. PubMed
  14. Studniberg SI, et al. 2022. Mol Syst Biol. 18:e10824. PubMed
  15. Koikawa K, et al. 2021. Cell. 184:4753. PubMed
  16. Katagiri T, et al. 2019. Mucosal Immunol. 12:p1104. PubMed
  17. Severance AL, et al. 2022. iScience. 25:104400. PubMed
  18. Takenori Inomata, Jing Hua, Antonio Di Zazzo 2016. Sci Rep. 6:39924. PubMed
  19. Fan MY et al. 2018. Cell reports. 25(5):1204-1213 . PubMed
  20. Fedele C, et al. 2021. J Exp Med. 218: . PubMed
  21. Henkle TR, et al. 2021. Cancer Res. 81:4560. PubMed
  22. Long L, et al. 2021. Nature. 600:308. PubMed
RRID
AB_2087653 (BioLegend Cat. No. 106309)
AB_2087653 (BioLegend Cat. No. 106310)

Antigen Details

Structure
Ig superfamily, 33 kD
Distribution

Activated T cells and B cells

Function
Negative regulator of T cell activation
Ligand/Receptor
CD80 (B7-1), CD86 (B7-2)
Cell Type
B cells, T cells, Tregs
Biology Area
Immunology
Molecular Family
CD Molecules, Immune Checkpoint Receptors
Antigen References

1. Barclay A, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Allison JP, et al. 1995. Science 270:932.
3. Waterhouse P, et al. 1995. Science 270:985.
4. Linsley PS, et al. 1991. J. Exp. Med. 174:561.

Gene ID
12477 View all products for this Gene ID
UniProt
View information about CD152 on UniProt.org

Related FAQs

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Go To Top Version: 2    Revision Date: 04.18.2014

For Research Use Only. Not for diagnostic or therapeutic use.

 

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This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

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