Anti-Mouse CD275 (B7-H2) PE

Also known as: B7RP-1, B7RP1, ICOS-L, ICOSL, GL50, B7H2

Clone: HK5.3

RUO: For Research Use Only. Not for use in diagnostic procedures.

SKU# 12-5985

Cat. No. Size
12-5985-81 50 ug
12-5985-82 100 ug
12-5985-83 200 ug
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Data for Anti-Mouse CD275 (B7-H2) PE.

Staining of BALB/c splenocytes with Anti-Mouse CD3e FITC (cat. 11-0031) and staining buffer...View More

  • Data for Anti-Mouse CD275 (B7-H2) PE.
Description

Description: The HK5.3 monoclonal antibody reacts with mouse B7RP-1, also known as B7h, B7-H2, GL50 and ICOS Ligand. B7RP-1, a member of the B7 family, has a predicted molecular weight of ~40 kDa and belongs to the Ig superfamily. Mouse B7RP-1 is expressed by antigen presenting cells including B cells, monocytes/macrophages and dendritic cells. B7RP-1 binds to the ICOS molecule (AILIM, CRP-1) expressed by activated T cells. The interaction of ICOS/B7RP-1 plays an important role in the T cell costimulation pathway.

Details
Host Rat
Isotype IgG2a, kappa
Reactivity Mouse
Conjugate PE
Laser Blue Laser, Green Laser, Yellow-Green Laser
Emit 575 nm
Excite 488 - 561 nm
Reported Applications Flow Cytometric Analysis
Documentation
TDS Link Download TDS
Additional Formats
Cat. No. Name Excite Emit Application Reg.
13-5985 Anti-Mouse CD275 (B7-H2) Biotin FC RUO
14-5985 Anti-Mouse CD275 (B7-H2) Purified FC, FA RUO
16-5985 Anti-Mouse CD275 (B7-H2) Functional Grade Purified FC, FA RUO
Related Products
Cat. No. Name Excite Emit Application Reg.
11-0031 Anti-Mouse CD3e FITC 488 nm FC RUO
12-4321 Rat IgG2a K Isotype Control PE 488 - 561 nm FC RUO
References

References: Iwai H, Kozono Y, et al. 2002. Amelioration of collagen-induced arthritis by blockade of inducible costimulator-b7 homologous protein costimulation. J Immunol. 169(8): 4332-9. Carreno BM, Collins M. 2002. THE B7 FAMILY OF LIGANDS AND ITS RECEPTORS: New Pathways for Costimulation and Inhibition of Immune Responses. Annu Rev Immunol. 20: 29-53. Liu X, Bai XF, et al. 2001. B7H costimulates clonal expansion of, and cognate destruction of tumor cells by, CD8(+) T lymphocytes in vivo. J Exp Med. 194(9): 1339-48.