CD42d/GPV Polyclonal Antibody

    • Catalog No.:YT5587
    • Applications:WB;IHC;IF;FC;ELISA
    • Reactivity:Human;Mouse;Rat
      • Target:
      • CD42d
      • Fields:
      • >>ECM-receptor interaction;>>Platelet activation;>>Hematopoietic cell lineage
      • Gene Name:
      • GP5
      • Protein Name:
      • Platelet glycoprotein V
      • Human Gene Id:
      • 2814
      • Human Swiss Prot No:
      • P40197
      • Mouse Swiss Prot No:
      • O08742
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from the Internal region of human GP5. AA range:331-380
      • Specificity:
      • CD42d Polyclonal Antibody detects endogenous levels of CD42d protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. IHC: 1:100-1:300. ELISA: 1:10000.. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • GP5;Platelet glycoprotein V;GPV;Glycoprotein 5;CD42d
      • Observed Band(KD):
      • 62kD
      • Background:
      • Human platelet glycoprotein V (GP5) is a part of the Ib-V-IX system of surface glycoproteins that constitute the receptor for von Willebrand factor (VWF; MIM 613160) and mediate the adhesion of platelets to injured vascular surfaces in the arterial circulation, a critical initiating event in hemostasis. The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9; MIM 173515) and GP5. Mutations in GP1BA, GP1BB, and GP9 have been shown to cause Bernard-Soulier syndrome (MIM 231200), a bleeding disorder (review by Lopez et al., 1998 [PubMed 9616133]).[supplied by OMIM, Nov 2010],
      • Function:
      • function:The GPIb-V-IX complex functions as the vWF receptor and mediates vWF-dependent platelet adhesion to blood vessels. The adhesion of platelets to injured vascular surfaces in the arterial circulation is a critical initiating event in hemostasis.,PTM:The N-terminus is blocked.,similarity:Contains 14 LRR (leucine-rich) repeats.,tissue specificity:Platelets and megakaryocytes.,
      • Subcellular Location:
      • Membrane; Single-pass type I membrane protein.
      • Expression:
      • Platelets and megakaryocytes.
      • Products Images
      • Enhanced Proliferation of Visualizable Mesenchymal Stem Cell–Platelet Hybrid Cell for Versatile Intracerebral Hemorrhage Treatment ACS Nano Dai-Wen Pang WB,IF,FC Mouse platelets (PLs),mesenchymal stem cells (MSCs),fusion cells(FCs)
      • Enhanced Proliferation of Visualizable Mesenchymal Stem Cell–Platelet Hybrid Cell for Versatile Intracerebral Hemorrhage Treatment ACS Nano Dai-Wen Pang WB,IF,FC Mouse platelets (PLs),mesenchymal stem cells (MSCs),fusion cells(FCs)
      • Western Blot analysis of Hela cells using CD42d Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
      • Immunohistochemical analysis of paraffin-embedded human-tonsils, antibody was diluted at 1:100