CXCR4 Mouse Monoclonal Antibody [Clone ID: B-R24]

CAT#: AM31204PU-N

CXCR4 mouse monoclonal antibody, clone B-R24, Purified

Product Images

A typical staining pattern with the B-R24 monoclonal antibody of lymphocytes.

Specifications

Product Data

• Clone Name: B-R24
• Applications: FC
• Recommended Dilution: Flow Cytometry: Use 10 µl to label 10e6 cells or 100 µl of whole blood.
• Reactivities: Human
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: CXCR4 transfected CHO cell line.
  Hybridoma: Myeloma X63/AG.8653 x Balb/c spleen cells.
• Specificity: Recognizes the soluble antigen.
  Recognizes the CXCR4 antigen, a 39.7 kDa protein.
• Formulation: PBS containing 1% BSA as stabilizer and 0.09% Sodium Azide as preservative
  State: Purified
  State: Liquid purified IgG fraction.
• Purification: Ion Exchange Chromatography.
• Gene Name: Homo sapiens chemokine (C-X-C motif) receptor 4 (CXCR4), transcript variant 1
• Database Link:
  Entrez Gene 7852 Human
• Background: CXCR4 (fusin, LESTR or HUMSTR) is a principal coreceptor for T cell tropic strains of HIV1 fusion and entry of human white blood cells. CXCR4 is also required for the infection by dual tropic strains of HIV1 and mediates CD4 independent infection by HIV2. The a chemokine SDF1 is the ligand for CXCR4 and prevents infection by T tropic HIV1. CXCR4 associates with the surface CD4-gp120 complex before HIV enters target cells. CXCR4 messenger RNA levels correlated with HIV1 permissiveness in diverse human cell types. Antibodies to CXCR4 block HIV1 and HIV2 fusion and infection of human target cells. The amino terminal domain and the second extracellular loop of CXCR4 serve as HIV biding sites. CXCR4 is highly expressed in brain and heart, and in white blood cells, vascular endothelial cells, and umbilical cord endothelial cells.
• Synonyms: CXC-R4, CXCR-4, Fusin, LCR1, FB22, NPYRL, HM89, SDF1 receptor, LESTR

Reference Data

• Protein Families: Druggable Genome, ES Cell Differentiation/IPS, GPCR, Transmembrane
• Protein Pathways: Axon guidance, Chemokine signaling pathway, Cytokine-cytokine receptor interaction, Endocytosis, Leukocyte transendothelial migration