GP1BA monoclonal antibody, clone HIP1
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Specifications
Product Description
Mouse monoclonal antibody raised against native purified human GP1BA (CD42b) from peripheral blood mononuclear cells.
Immunogen
Native purified human GP1BA.
Host
Mouse
Reactivity
Human, Mouse, Primates
Form
Liquid
Purification
Protein A purification
Isotype
IgG1
Recommend Usage
CyTOF
Flow Cytometry 1-4 ug/mL
Immunohistochemistry (1:10-1:500)
Immunohistochemistry-Frozen (1:200)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH7.4 (0.05% Sodium Azide).
Storage Instruction
Store at 4°C.
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Applications
Immunohistochemistry (Frozen sections)
Immunohistochemistry
Flow Cytometry
Flow cytometric analysis of human platelets with GP1BA monoclonal antibody, clone HIP1 (Cat # MAB23340).Mass Cytometry
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Gene Info — GP1BA
Entrez GeneID
2811Gene Name
GP1BA
Gene Alias
BSS, CD42B, CD42b-alpha, GP1B, MGC34595
Gene Description
glycoprotein Ib (platelet), alpha polypeptide
Gene Ontology
HyperlinkGene Summary
Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that are linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Several polymorphisms and mutations have been described in this gene, some of which are the cause of Bernard-Soulier syndromes and platelet-type von Willebrand disease. [provided by RefSeq
Other Designations
platelet glycoprotein Ib alpha polypeptide|platelet membrane glycoprotein 1b-alpha subunit
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Interactomes
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Pathways
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Diseases
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