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Purified 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
UC10-4B9_Purified_CD152_Antibody_052819_updated.png
Con A+IL-2-stimulated C57BL/6 splenocytes (3 days) were stained with CD3 APC and CD152 (clone UC10-4B9) Purified (left) or Purified Armenian Hamster IgG isotype control (right) followed by PE anti-Armenian Hamster IgG.
  • UC10-4B9_Purified_CD152_Antibody_052819_updated.png
    Con A+IL-2-stimulated C57BL/6 splenocytes (3 days) were stained with CD3 APC and CD152 (clone UC10-4B9) Purified (left) or Purified Armenian Hamster IgG isotype control (right) followed by PE anti-Armenian Hamster IgG.
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106302 500 µg 184€
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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 (pdf)

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.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

FC - Quality tested
IP, ELISA, Block - Reported in the literature, not verified in house
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.

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. Liu CJ, et al. 2020. Neuro Oncol. 22:1276. PubMed
  2. Moore AR, et al. 2022. Cell Rep. 41:111651. PubMed
  3. Hezaveh K, et al. 2022. Immunity. 55:324. PubMed
  4. Hu J, et al. 2019. Am J Transl Res. 3.043055556. PubMed
  5. Goel S, et al. 2017. Nature. 548:471. PubMed
  6. Wei SC et al. 2017. Cell. 170(6):1120-1133 . PubMed
  7. Wei SC, et al. 2019. Immunity. 50:1084. PubMed
  8. Sato Y, et al. 2021. BMC Cancer. 21:1222. PubMed
  9. Yang K, et al. 2017. Nature. 548:602. PubMed
  10. Sun Y, et al. 2020. J Immunol. 205:3358. PubMed
  11. Sprouse ML, et al. 2018. JCI Insight. 3:e97322. PubMed
  12. Muhammad F, et al. 2020. J Autoimmun. 111:102441. PubMed
  13. Gubin MM, et al. 2018. Cell. 175:1014. PubMed
  14. Rosenbaum M, et al. 2019. Nat Commun. 2.05. PubMed
  15. Jiao S, et al. 2020. Cell. 179(5):1177-1190.e13.. PubMed
  16. Sudan R, et al. 2022. Front Immunol. 13:830961. PubMed
  17. Xu W, et al. 2021. Immunity. 54(3):526-541.e7. PubMed
RRID
AB_313251 (BioLegend Cat. No. 106302)

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

There are no FAQs for this product.
Go To Top Version: 1    Revision Date: 11/30/2012

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

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
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