Recombinant Human GP1BA Protein, His-tagged
Cat.No. : | GP1BA-683H |
Product Overview : | Recombinant Human GP1BA Protein (Ile19-Leu291) with His tag was expressed in 293F. |
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Description : | Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that is 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. Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease. The coding region of this gene is known to contain a polymophic variable number tandem repeat (VNTR) domain that is associated with susceptibility to nonarteritic anterior ischemic optic neuropathy. |
Source : | HEK293F |
Species : | Human |
Tag : | N-His |
Form : | Freeze-dried powder |
Molecular Mass : | Predicted Molecular Mass: 31.8 kDa; Accurate Molecular Mass: 38-44 kDa |
Protein length : | Ile19-Leu291 |
Purity : | > 95% |
Applications : | Positive Control; Immunogen; SDS-PAGE; WB. |
Stability : | The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 centigrade for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8 centigrade for one month. Aliquot and store at -80 centigrade for 12 months. |
Storage Buffer : | 20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% SKL, 5% Trehalose and Proclin300. |
Reconstitution : | Reconstitute in 20mM Tris, 150mM NaCl (pH8.0) to a concentration of 0.1-1.0 mg/mL. Do not vortex. |
Gene Name : | GP1BA glycoprotein Ib platelet subunit alpha [ Homo sapiens (human) ] |
Official Symbol : | GP1BA |
Synonyms : | GP1BA; glycoprotein Ib platelet subunit alpha; BSS; GP1B; VWDP; CD42B; GPIbA; BDPLT1; BDPLT3; DBPLT3; GPIbalpha; CD42b-alpha; platelet glycoprotein Ib alpha chain; GP-Ib alpha; antigen CD42b-alpha; glycoprotein Ib (platelet), alpha polypeptide; glycoprotein Ib platelet alpha subunit; mutant platelet membrane glycoprotein Ib-alpha; platelet membrane glycoprotein 1b-alpha subunit; platelet membrane glycoprotein Ib-alpha |
Gene ID : | 2811 |
mRNA Refseq : | NM_000173 |
Protein Refseq : | NP_000164 |
MIM : | 606672 |
UniProt ID : | P07359 |
Products Types
◆ Recombinant Protein | ||
GP1BA-16H | Recombinant Human GP1BA Protein, His-tagged | +Inquiry |
GP1BA-2584H | Recombinant Human GP1BA protein(381-450 aa), N-SUMO & C-His-tagged | +Inquiry |
GP1BA-5130H | Recombinant Human GP1BA Protein, GST-tagged | +Inquiry |
GP1BA-531H | Recombinant Human GP1BA Protein (17-505 aa), His-tagged | +Inquiry |
GP1BA-1401H | Recombinant Human GP1BA Protein (17-531 aa), His-tagged | +Inquiry |
◆ Lysates | ||
GP1BA-5823HCL | Recombinant Human GP1BA 293 Cell Lysate | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (7)
Ask a questionGlycoprotein Ib platelet subunit alpha (GP1BA) plays a crucial role in platelet physiology and hemostasis, specifically in platelet adhesion.
Dysregulation or abnormal expression of GP1BA is associated with conditions such as Bernard-Soulier syndrome and other platelet disorders.
GP1BA contributes to platelet adhesion by interacting with von Willebrand factor (vWF), facilitating platelet plug formation at vascular injury sites.
Interactions or binding partners of GP1BA include vWF and other components of the platelet glycoprotein Ib-IX-V complex, influencing platelet function.
GP1BA participates in the regulation of blood clotting and coagulation cascades by initiating platelet activation and aggregation.
GP1BA is predominantly localized on the surface of platelets, especially within the platelet membrane.
There are potential therapeutic implications related to GP1BA in diseases involving platelet disorders, making it a target for drug development.
Customer Reviews (3)
Write a reviewIts compatibility with collaborative platforms and open-source tools facilitated sharing and reproducibility of our experiments.
The product's support in the form of educational resources positively impacted the learning curve for our researchers.
The product's track record of being featured in influential publications positively influenced our decision to use it.
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