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FACS analysis of human peripheral blood using GTX15021 CD41a antibody [HIP8].
FACS analysis of human peripheral blood using GTX15021 CD41a antibody [HIP8].
FACS analysis of human peripheral blood using GTX15021 CD41a antibody [HIP8].

CD41 antibody [HIP8]

GTX15021
GeneTex
ApplicationsFlow Cytometry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen
Product group Antibodies
ReactivityHuman, Primate
TargetITGA2B
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Overview

  • Supplier
    GeneTex
  • Product Name
    CD41 antibody [HIP8]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody reacts with alpha (a) subunit of CD41 (heavy chain; 120 kDa). The antibody HIP8 blocks platelet aggregation and completely inhibits ADP-, epinephrine-, and collagen-induced platelet activation, and partially inhibits ristocetin- and thrombin
  • Applications
    Flow Cytometry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    HIP8
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3674
  • Target name
    ITGA2B
  • Target description
    integrin subunit alpha 2b
  • Target synonyms
    alphaIIb protein; BDPLT16; BDPLT2; CD41; CD41B; GP2B; GPalpha IIb; GPIIb; GT; GT1; GTA; HPA3; integrin alpha-IIb; integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41); platelet fibrinogen receptor, alpha subunit; platelet glycoprotein IIb of IIb/IIIa complex; platelet membrane glycoprotein IIb; platelet-specific antigen BAK; PPP1R93; protein phosphatase 1, regulatory subunit 93
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP08514
  • Protein Name
    Integrin alpha-IIb
  • Scientific Description
    This gene encodes a member of the integrin alpha chain family of proteins. The encoded preproprotein is proteolytically processed to generate light and heavy chains that associate through disulfide linkages to form a subunit of the alpha-IIb/beta-3 integrin cell adhesion receptor. This receptor plays a crucial role in the blood coagulation system, by mediating platelet aggregation. Mutations in this gene are associated with platelet-type bleeding disorders, which are characterized by a failure of platelet aggregation, including Glanzmann thrombasthenia. [provided by RefSeq, Jan 2016]
  • Reactivity
    Human, Primate
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203