产品名称:PE-Cy™7 小鼠抗人 CD8 抗体;PE-Cy™7 Mouse Anti-Human CD8
中文名称:PE-Cy™7 小鼠抗人 CD8 抗体
英文名称:PE-Cy™7 Mouse Anti-Human CD8
PE-Cy™7 Mouse Anti-Human CD8 产品介绍:
Material Number: 557746 Alternate Name: CD8α; CD8A; CD8 alpha; Leu2; MAL; T8; p32 Size: 100 Tests Vol. per Test: 5 µl Clone: RPA-T8 Isotype: Mouse IgG1, κ Reactivity: QC Testing: Human Tested in Development: Rhesus, Cynomolgus, Baboon Workshop: IV T171; V T-CD08.03; VI 6T-CD8.1, 6T-081 Storage Buffer: Aqueous buffered solution containing BSA and ≤0.09% sodium azide. PE-Cy™7 Mouse Anti-Human CD8 Description:
The RPA-T8 monoclonal antibody specifically binds to CD8 alpha (CD8α). CD8α is a type I transmembrane glycoprotein and a member of the immunoglobulin superfamily. CD8α is expressed by the majority of thymocytes, by subpopulations of αβ T cells and γδ T cells and by some NK cells. Cell surface CD8α is expressed either as a disulfide-linked homodimer (CD8αα) or as a heterodimer (CD8αβ) when disulfide-bonded to a CD8 beta chain (CD8β). CD8-positive αβ T cells coexpress both CD8αα homodimers and CD8αβ heterodimers whereas some γδ T cells and NK cells express CD8αα homodimers. CD8 plays important roles in T cell activation and selection. The extracellular IgSF domain of CD8α binds to a non-polymorphic determinant on HLA class I molecules (α3 domain) and enables CD8 to function as a co-receptor with MHC class I-restricted TCR during T cell recognition of antigen. The cytoplasmic domain of CD8α associates with Lck, a Src family protein tyrosine kinase that is involved in intracellular signaling. The RPA-T8 and HIT8a monoclonal antibodies are not cross-blocking. This clone has been reported to react with a subset of peripheral blood lymphocytes, but not monocytes nor granuloyctes, of baboon and both rhesus and cynomolgus macaque monkey. In general, a higher frequency of CD8+ and CD4+CD8+ lymphocytes are observed in non-human primates compared to normal human donors.
Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated with PE-Cy7 under optimum conditions, and unconjugated antibody and free PE-Cy7 were removed.
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