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APC anti-mouse CD80 Antibody

Pricing & Availability
Clone
16-10A1 (See other available formats)
Regulatory Status
RUO
Other Names
B7-1, B7, Ly-53
Isotype
Armenian Hamster IgG
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Product Citations
publications
16-10A1_APC_CD80_Antibody_FC_091014.jpg
LPS-stimulated (3 days) BALB/c splenocytes were stained with CD80 (clone 16-10A1) APC (filled histogram) or Armenian hamster IgG APC isotype control (open histogram).
  • 16-10A1_APC_CD80_Antibody_FC_091014.jpg
    LPS-stimulated (3 days) BALB/c splenocytes were stained with CD80 (clone 16-10A1) APC (filled histogram) or Armenian hamster IgG APC isotype control (open histogram).
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104713 25 µg 71€
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104714 100 µg 212€
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Description

CD80 is a 60 kD highly glycosylated protein. It is a member of the Ig superfamily and is also known as B7-1, B7, and Ly-53. CD80 is constitutively expressed on dendritic cells and monocytes/macrophages, and inducibly expressed on activated B and T cells. The ligation of CD28 on T cells with CD80 and CD86 (B7-2) on antigen presenting cells (such as dendritic cells, macrophages, and B cells) elicits co-stimulation of T cells resulting in enhanced cell activation, proliferation, and cytokine production. CD80 appears to be expressed later in the immune response than CD86. CD80 can also bind to CD152, also known as CTLA-4, to deliver an inhibitory signal to T cells.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Reported Reactivity
Dog
Antibody Type
Monoclonal
Host Species
Armenian Hamster
Immunogen
CHO cell line transfected with mouse B7 (CD80)
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

Additional reported applications (for the relevant formats) include: immunoprecipitation2, in vitro and in vivo blocking of CTLA-4 Ig to CD80 by blocking costimulation of T cells by activated B cells2-4, and immunohistochemical staining of acetone-fixed frozen sections1,4. The Ultra-LEAF™ purified antibody (Endotoxin < 0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. Nos. 104747-104752).

Application References
  1. Harlan DM, et al. 1994. P. Natl. Acad. Sci. USA 91:3137. (IHC)
  2. Razi-Wolf Z, et al. 1992. P. Natl. Acad. Sci. USA 89:4210. (Block, IP)
  3. Hathcock KS, et al. 1994. J. Exp. Med. 180:631. (Block)
  4. Herold KC, et al. 1997. J. Immunol. 158:984. (Block, IHC)
  5. Ma XT, et al. 2006. Cancer Res. 66:1169.
  6. Andoniou CE, et al. 2005. Nature Immunology 6:1011. (FC)
  7. Lawson BR, et al. 2007. J. Immunol. 178:5366.
  8. Turnquist HR, et al. 2007. J. Immunol. 178:7018.
  9. Misra RS, et al. 2010. J. Exp Med. 207:1775. PubMed
  10. del Rio ML, et al. 2011. Transpl. Int. 24:501. (FC) PubMed
  11. Philipsen L, et al. 2013. Mol Cell Proteomics. 12:2551. PubMed
Product Citations
  1. Russler-Germain EV, et al. 2021. Immunity. 54:2547. PubMed
  2. Mi Z, et al. 2021. Vaccines (Basel). 10: . PubMed
  3. Zhu J, et al. 2022. Nat Commun. 13:7466. PubMed
  4. Yu J, et al. 2022. Nat Commun. 13:7903. PubMed
  5. Ding D, et al. 2023. J Med Chem. 66:1467. PubMed
  6. Yao RQ, et al. 2022. Theranostics. 12:4606. PubMed
  7. An S, et al. 2022. Int J Mol Sci. 23:. PubMed
  8. Català C, et al. 2022. iScience. 25:105078. PubMed
  9. Miao L, et al. 2020. Theranostics. 0.7625. PubMed
  10. Diao L, et al. 2022. iScience. 25:105511. PubMed
  11. Hreha TN, et al. 2020. Front Immunol. 1.597916667. PubMed
  12. Clement M, et al. 2016. PLoS Pathog. 12:e1006050. PubMed
  13. Tyagi AM et al. 2018. Immunity. 49(6):1116-1131 . PubMed
  14. Onodera T, et al. 2012. Proc Natl Acad Sci U S A. 109:2485. PubMed
  15. Britton GJ et al. 2019. Immunity. 50(1):212-224 . PubMed
  16. Wang Z, et al. 2021. J Virol. 95:e0141421. PubMed
  17. Ma J, et al. 2021. Curr Protoc. 1:e144. PubMed
  18. Škrnjug I, et al. 2014. PLoS One. 9:110150. PubMed
  19. Jeljeli M, et al. 2020. Cell Rep. 33:108325. PubMed
  20. Uchil PD et al. 2018. Cell host & microbe. 25(1):87-100 . PubMed
  21. Terashima Y, et al. 2020. Nat Commun. 11:609. PubMed
  22. Stewart JM, et al. 2020. ACS Biomater Sci Eng. 6:5941. PubMed
  23. Russler-Germain EV, et al. 2021. Elife. 10:. PubMed
  24. Onodera T, et al. 2016. J Immunol. 196: 4172 - 4184. PubMed
  25. Horiguchi H, et al. 2019. Genes Dev. 33:1641. PubMed
  26. Carbone C, et al. 2021. J Immunother Cancer. 9:. PubMed
  27. Mao L, et al. 2022. Front Immunol. 13:833418. PubMed
  28. Xue RY, et al. 2019. Front Immunol. 10:1372. PubMed
  29. Han F, et al. 2020. Invest Ophthalmol Vis Sci. 61:24. PubMed
  30. Chou S, et al. 2016. J Control Release. 244:14-23. PubMed
  31. Assi H, et al. 2014. PLoS One. 9:96318. PubMed
  32. Olson WJ, et al. 2019. Cell Rep. 28:2878. PubMed
  33. Guan X, et al. 2022. Nat Commun. 13:2834. PubMed
  34. Feng Y, et al. 2022. J Nanobiotechnology. 20:193. PubMed
  35. Zhang S, et al. 2022. Nat Commun. 13:4744. PubMed
  36. Ghorbani S, et al. 2022. Nat Commun. 13:2445. PubMed
  37. Wang X, et al. 2022. J Biol Chem. 298:101561. PubMed
  38. Yi H, et al. 2021. Front Immunol. 12:719189. PubMed
  39. Gong N, et al. 2020. Nat Nanotechnol. 1.35625. PubMed
  40. Zhang J, et al. 2022. Biomater Res. 26:44. PubMed
  41. Zhao Y, et al. 2020. Immunity. 51(6):1059-1073.e9.. PubMed
  42. Hollern DP, et al. 2020. Cell. 179(5):1191-1206.e21.. PubMed
  43. Molina MS, et al. 2021. Front Immunol. 12:699128. PubMed
  44. Peng KT, et al. 2019. Int J Nanomedicine. 14:469. PubMed
  45. Xu Y, et al. 2021. iScience. 24:103445. PubMed
  46. Singhal P, et al. 2016. Proc Natl Acad Sci U S A. 113: 122 - 127. PubMed
  47. Knox T, et al. 2019. Sci Rep. 9:6136. PubMed
  48. Lavoie S, et al. 2020. Gastroenterology. 158:1359. PubMed
  49. Mino T, et al. 2019. Nucleic Acids Res. 47:8838. PubMed
  50. Guo S, et al. 2021. Chronic Dis Transl Med. 7:254. PubMed
  51. Angulo G, et al. 2021. eLife. 10:00. PubMed
  52. Lucas ED, et al. 2020. Cell Reports. 33(2):108258. PubMed
  53. Chng S, et al. 2016. Sci Rep. 6: 23820. PubMed
RRID
AB_313135 (BioLegend Cat. No. 104713)
AB_313135 (BioLegend Cat. No. 104714)

Antigen Details

Structure
Ig superfamily, 60 kD
Distribution

Macrophages, activated B cells and T cells, dendritic cells

Function
T cell costimulation
Ligand/Receptor
CD28 (stimulatory), CD152(CTLA4) (inhibitory)
Cell Type
B cells, Dendritic cells, Macrophages, T cells, Tregs
Biology Area
Cell Biology, Costimulatory Molecules, Immunology, Neuroscience, Neuroscience Cell Markers
Molecular Family
CD Molecules, Immune Checkpoint Receptors
Antigen References

1. Barclay AN, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Linsley PS, et al. 1991. J. Exp. Med. 174:561.
3. Salomon B, et al. 2001. Annu. Rev. Immunol. 19:225.

Gene ID
12519 View all products for this Gene ID
UniProt
View information about CD80 on UniProt.org
Go To Top Version: 4    Revision Date: 09/11/2014

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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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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