GP9 (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human GP9 full-length ORF ( AAH30229.1, 1 a.a. - 177 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MPAWGALFLLWATAEATKDCPSPCTCRALETMGLWVDCRGHGLTALPALPARTRHLLLANNSLQSVPPGAFDHLPQLQTLDVTQNPWHCDCSLTYLRLWLEDRTPEALLQVRCASPSLAAHGPLGRLTGYQLGSCGWQLQASWVRPGVLWDVALVTVAALGLALLAGLLCATTEALD
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
45.5
Interspecies Antigen Sequence
Mouse (72); Rat (69)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — GP9
Entrez GeneID
2815GeneBank Accession#
BC030229.1Protein Accession#
AAH30229.1Gene Name
GP9
Gene Alias
CD42a, GPIX
Gene Description
glycoprotein IX (platelet)
Gene Ontology
HyperlinkGene Summary
This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency. [provided by RefSeq
Other Designations
platelet glycoprotein IX
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Interactome
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Pathway
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Disease
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