The 2.4G2 antibody reacts specifically with a common nonpolymorphic epitope on the extracellular domains of the mouse FcγIII and FcγII receptors. It has also been reported to bind the FcγI receptor (CD64) via its Fc domain. 2.4G2 mAb blocks non-antigen-specific binding of immunoglobulins to the FcγIII and FcγII, and possibly FcγI, receptors in vitro and in vivo. CD16 and/or CD32 are expressed on natural killer cells, monocytes, macrophages, dendritic cells (at low levels), Kupffer cells, granulocytes, mast cells, B lymphocytes, immature thymocytes, and some activated mature T lymphocytes. This antibody is routinely tested by flow cytometric analysis. Other applications were tested during antibody development only or reported in the literature. Two color analysis of the expression of CD16/CD32 on mouse spleen cells and demonstration of FCγR-mediated non-specific staining. Left: BALB/c splenocytes were simultaneously stained with PE-conjugated anti-mouse CD3e mAb 145-2C11 (Cat. No. 553063/553064) and purified 2.4G2 mAb. The staining by 2.4G2 antibody was detected with FITC-conjugated mouse anti-rat lg, κ chain mAb MRK-1 (Cat. No. 553872). Right: BALB/c splenocytes were stained with FITC-conjugated rat anti-mouse CD90.2 (Thy-1.2) mAb 53-2.1 (Cat. No. 553003/553004) in the presence of purified 2.4G2 mAb (filled histogram) and without 2.4G2 mAb (open histogram). Flow cytometry was performed on a BD FACScan™ flow cytometry system.
BD Pharmingen™ Purified Rat Anti-Mouse CD16/CD32 (Mouse BD Fc Block™) - Purified - Clone 2.4G2 - Isotype Rat IgG2b, κ - Reactivity Ms - 0.1 mg
Aufreinigung
The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Lagerung
4 °C
Informationen zur Lagerung
Store undiluted at 4°C.
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