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PE/Cyanine7 anti-mouse CD86 Antibody

Pricing & Availability
Clone
GL-1 (See other available formats)
Regulatory Status
RUO
Other Names
B7-2, B70, Ly-58
Isotype
Rat IgG2a, κ
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Product Citations
publications
GL-1_PECy7_090707
C57BL/6 mouse splenocytes stained with GL-1 PE/Cyanine7
  • GL-1_PECy7_090707
    C57BL/6 mouse splenocytes stained with GL-1 PE/Cyanine7
Compare all formats See PE/Cyanine7 spectral data
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105013 25 µg $94
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105014 100 µg $282
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Description

CD86 is an 80 kD immunoglobulin superfamily member also known as B7-2, B70, and Ly-58. CD86 is expressed on activated B and T cells, macrophages, dendritic cells, and astrocytes. CD86, along with CD80, is a ligand of CD28 and CD152 (CTLA-4). CD86 is expressed earlier in the immune response than CD80. CD86 has also been shown to be involved in immunoglobulin class-switching and triggering of NK cell-mediated cytotoxicity. CD86 binds to CD28 to transduce co-stimulatory signals for T cell activation, proliferation, and cytokine production. CD86 can also bind to CD152, also known as CTLA-4, to deliver an inhibitory signal to T cells.

Product Details
Technical data sheet

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
LPS-activated CBA/Ca mouse splenic B cells
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with PE/Cyanine7 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
Blue Laser (488 nm)
Green Laser (532 nm)/Yellow-Green Laser (561 nm)
Application Notes

The GL-1 antibody can block the mixed lymphocyte reaction in vitro and has been shown to inhibit the priming of cytotoxic T lymphocytes in vivo (along with antibodies against B7-1). Additional reported applications (for the relevant formats) include: immunoprecipitation1, immunohistochemical staining of acetone-fixed frozen sections2,6, immunofluorescence microscopy, and in vivo and in vitro blocking of T cell responses1-6. GL-1 is not suitable for immunohistochemical staining of formalin-fixed paraffin sections. The Ultra-LEAF™ purified antibody (Endotoxin < 0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. No. 105051-105056).

Application References

(PubMed link indicates BioLegend citation)
  1. Hathcock KS, et al. 1993. Science 262:905. (Block, IP)
  2. Inaba KM, et al. 1994. J. Exp. Med. 180:1849. (Block, IHC)
  3. Hathcock KS, et al. 1994. J. Exp. Med. 180:631. (Block)
  4. Krummel MF, et al. 1995. J. Exp. Med. 182:459. (Block)
  5. Liu Y, et al. 1997. J. Exp. Med. 185:251. (Block)
  6. Herold KC, et al. 1997. J. Immunol. 158:984. (Block, IHC)
  7. Shih FF, et al. 2006. J. Immunol. 176:3438. (FC)
  8. Lawson BR, et al. 2007. J. Immunol. 178:5366.
  9. Turnquist HR, et al. 2007. J. Immunol. 178:7018.
  10. Klinger MB, et al. 2007. Am. J. Physiol. Requl. Integr. Comp. Physiol. 293:R677. PubMed
  11. de Verteuil DA, et al. 2014. J Immunol. 193:1121. PubMed
Product Citations
  1. Kuo PC, et al. 2021. Brain Commun. 3:fcab187. PubMed
  2. Zhang Z, et al. 2022. Front Pharmacol. 13:906625. PubMed
  3. Leung W, et al. 2022. Cancer Discov. 12:1782. PubMed
  4. Wang L, et al. 2022. Cell Rep. 41:111462. PubMed
  5. Xie Z, et al. 2022. Cell Discov. 8:133. PubMed
  6. Fan R, et al. 2023. J Immunother Cancer. 11: . PubMed
  7. Jiang X, et al. 2023. Cell Discov. 9:7. PubMed
  8. Ju C, et al. 2023. Cell Mol Biol Lett. 28:5. PubMed
  9. Fontana MF, et al. 2023. Elife. 12: . PubMed
  10. Grenov A, et al. 2022. Cell Rep. 39:110778. PubMed
  11. Zhang Y, et al. 2023. Invest Ophthalmol Vis Sci. 64:1. PubMed
  12. Cheng K, et al. 2023. Small. 19:e2300125. PubMed
  13. Ma X, et al. 2023. Nat Commun. 14:1606. PubMed
  14. Shi Y, et al. 2023. Nat Commun. 14:1884. PubMed
  15. Hsieh MS, et al. 2023. NPJ Vaccines. 8:82. PubMed
  16. Giorgetti E, et al. 2020. Cell Reports. 29(6):1539-1554.e7.. PubMed
  17. Amir M, et al. 2020. Biochem Biophys Res Commun. 527:1000. PubMed
  18. Liang S, et al. 2022. Acta Pharm Sin B. 12:2494. PubMed
  19. Limon JJ et al. 2019. Cell host & microbe. 25(3):377-388 . PubMed
  20. Kim CC et al. 2019. Cell Rep. 27(5):1446-1460 . PubMed
  21. Zhao J, et al. 2019. Nat Commun. 10:899. PubMed
  22. Oyarce C, et al. 2018. Front Immunol. 8:1794. PubMed
  23. Clement M, et al. 2016. PLoS Pathog. 12:e1006050. PubMed
  24. Palm A, et al. 2016. Sci Rep. 10.1038/srep20531. PubMed
  25. Xu AQ, et al. 2020. Elife. 9:00. PubMed
  26. Li K, et al. 2022. J Immunother Cancer. 10:. PubMed
  27. Terashima Y, et al. 2020. Nat Commun. 11:609. PubMed
  28. Ly A, et al. 2020. Cell Reports. 29(8):2257-2269.e6.. PubMed
  29. Dane EL, et al. 2022. Nat Mater. 21:710. PubMed
  30. Wang B, et al. 2022. Nat Commun. 13:3821. PubMed
  31. Zhang X, et al. 2022. Cells. 11:. PubMed
  32. Park HB, et al. 2020. Oncoimmunology. 9:1772663. PubMed
  33. Nguyen TKT, et al. 2020. Am J Pathol. 286:190. PubMed
  34. Zhang P, et al. 2022. BMC Med. 20:435. PubMed
  35. Li Z, et al. 2022. J Exp Clin Cancer Res. 41:74. PubMed
  36. Jeong SH, et al. 2021. Nat Commun. 12:4405. PubMed
  37. Polavaram NS, et al. 2021. Bone Res. 9:24. PubMed
  38. Wang J, et al. 2021. Nat Commun. 12:6198. PubMed
  39. Pardy RD, et al. 2021. Nat Commun. 12:4051. PubMed
  40. Schoeler K, et al. 2019. FEBS J. 10.1111/febs.14934. PubMed
  41. Tavazoie MF, et al. 2018. Cell. 172:825. PubMed
  42. Trabucco S, Gerstein R, Zhang H 2016. J Immunol. 197: 1699 - 1707. PubMed
  43. Guo L, et al. 2021. Vaccines (Basel). 9:. PubMed
  44. Pilones KA, et al. 2020. Cancer Immunol Res. 8:1054. PubMed
  45. Zhang J, et al. 2018. Sci Rep. 8:2373. PubMed
  46. Fox C, et al. 2016. J Control Release. 244:98-107. PubMed
  47. Anger-Góra N, et al. 2021. Oncol Lett. 22:582. PubMed
  48. Olson WJ, et al. 2019. Cell Rep. 28:2878. PubMed
  49. Lee W, et al. 2021. PLoS Pathog. 17:e1009168. PubMed
  50. Zhang W, et al. 2020. Nat Commun. 11:1187. PubMed
  51. Toki S, et al. 2013. Nanomedicine. 9:1235. PubMed
  52. Kelly SH, et al. 2021. ACS Biomater Sci Eng. 7:1876. PubMed
  53. Tukaramrao DB, et al. 2021. Cancers (Basel). 13:. PubMed
  54. Yang X, et al. 2022. Front Immunol. 13:856230. PubMed
  55. Kumagai S, et al. 2020. Immunity. 53(1):187-203.e8. PubMed
  56. Ma Y, et al. 2022. Front Immunol. 13:816952. PubMed
  57. Zhou J, et al. 2022. Int J Oncol. 61: . PubMed
  58. Resch TK, et al. 2018. Sci Rep. 0.722916667. PubMed
  59. Baumann D, et al. 2020. Nat Commun. 1.969444444. PubMed
  60. Cerina M, et al. 2017. Brain Behav Immun. 59:103-117. PubMed
  61. Qi H, et al. 2020. Cell Reports. 31(6):107621. PubMed
  62. Lee C, et al. 2020. Front Immunol. 11:77. PubMed
  63. Han P, et al. 2020. Sci Adv. 6:eaaz1580. PubMed
  64. Ryu S, et al. 2021. eLife. 0.416666666666667. PubMed
  65. Smith LK, et al. 2021. Elife. 10:. PubMed
  66. Perper SJ, et al. 2019. J Immunol. 203:58. PubMed
  67. Lu H, et al. 2011. Toxicol Appl Pharmacol. 255:251. PubMed
  68. Zamora-Chimal J, et al. 2017. Immunobiology. 222(2):454-462. PubMed
  69. Gangoso E, et al. 2021. Cell. 184:2454. PubMed
  70. Chen S, et al. 2018. Nat Commun. 9:5298. PubMed
RRID
AB_439782 (BioLegend Cat. No. 105013)
AB_439782 (BioLegend Cat. No. 105014)

Antigen Details

Structure
Ig superfamily, 80 kD
Distribution

B cells and T cells (upregulated upon activation), macrophages, dendritic cells, and astrocytes

Function
T cell costimulation, Ig class-switching, NK cell cytotoxicity
Ligand/Receptor
CD28, CD152 (CTLA-4)
Cell Type
Astrocytes, 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 A, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Hathcock KS, et al. 1993. Science 262:905.
3. Freeman GJ, et al. 1993. Science 262:907.
4. Carreno BM, et al. 2002. Annu. Rev. Immunol. 20:29.

Gene ID
12524 View all products for this Gene ID
UniProt
View information about CD86 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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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.
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