ICAM1 monoclonal antibody, clone 15.2 (Biotin) View larger

ICAM1 monoclonal antibody, clone 15.2 (Biotin)

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Data sheet of ICAM1 monoclonal antibody, clone 15.2 (Biotin)

BrandAbnova
Product typePrimary antibodies
ReactivityHuman
Host speciesMouse
ApplicationsFlow Cyt

More info about ICAM1 monoclonal antibody, clone 15.2 (Biotin)

Brand: Abnova
Reference: MAB5507
Product name: ICAM1 monoclonal antibody, clone 15.2 (Biotin)
Product description: Mouse monoclonal antibody raised against native ICAM1.
Clone: 15.2
Isotype: IgG1
Gene id: 3383
Gene name: ICAM1
Gene alias: BB2|CD54|P3.58
Gene description: intercellular adhesion molecule 1
Immunogen: A mixture of native ICAM1 from Rheumatoid synovial cells and human monocytes.
Form: Liquid
Recommend dilutions: Flow Cytometry (using 1ug to stain 1 x 106 cells)
The optimal working dilution should be determined by the end user.
Storage buffer: In 10 mM PBS, pH 7.2 (1% BSA, 0.09% sodium azide)
Storage instruction: Store at 4°C. Do not freeze.
Note: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Conjugate tag: Biotin
Product type: Primary antibodies
Host species: Mouse
Antigen species / target species: Human
Specificity: Recognizes the (Mr 85-115KDa) intercellular adhesion molecule ICAM-1 which permits antigen-independent adhesion between lymphocytes and their targets. The LFA-1 binding site is located in domain 1 of ICAM-1. ICAM-1 is a membrane glycoprotein with a wide tissue distribution that includes vascular endothelium and many cells of the immune system. CD54 is weakly expressed on resting peripheral blood lymphocytes. Upon activation by mitogens, the CD54 antigen is strongly expressed on B-cells, T-cells, macrophages and granulocytes. CD54 is the receptor for rhinoviruses and malaria
Reactivity: Human
Applications: Flow Cyt
Shipping condition: Blue Ice
Publications: The binding site on ICAM-1 for Plasmodium falciparum-infected erythrocytes overlaps, but is distinct from, the LFA-1-binding site.Berendt AR, McDowall A, Craig AG, Bates PA, Sternberg MJ, Marsh K, Newbold CI, Hogg N.
Cell. 1992 Jan 10;68(1):71-81.

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