CD42d rabbit pAb

CD42d rabbit pAb

AO-06-ES4317-100

CD42d rabbit pAb 100μL

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€429.00
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Antibody Product Overview

ELK.NoES4317
Product nameCD42d rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameGP5; Platelet glycoprotein V; GPV; Glycoprotein 5; CD42d
Size100μL
Unit price ($)248
Human gene ID2814
Human Swiss-ProtP40197
SourceRabbit
IsotypeIgG
TargetCD42d
Fields>>ECM-receptor interaction;>>Platelet activation;>>Hematopoietic cell lineage
Gene nameGP5
Protein namePlatelet glycoprotein V
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtO08742
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25259
Rat gene linkView Rat Gene
Rat Swiss-ProtO08770
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human GP5. AA range:331-380
SpecificityCD42d Polyclonal Antibody detects endogenous levels of CD42d protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)62kD
BackgroundHuman 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],
Functionfunction: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 locationMembrane; Single-pass type I membrane protein.
ExpressionPlatelets and megakaryocytes.

Additional Images

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Western Blot analysis of Hela cells using CD42d Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-tonsils, antibody was diluted at 1:100
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: AO-06-ES4317-100
: 10 Items
Hurry! only 10 items left in stock.

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