SAB4200247
Anti-GP1BA antibody, Mouse monoclonal
clone PM6/40, purified from hybridoma cell culture
别名:
MonoclonalAnti-BSS, MonoclonalAnti-CD42B, MonoclonalAnti-CD42balpha, MonoclonalAnti-GP1B, MonoclonalAnti-MGC34595, MonoclonalAnti-glycoprotein Ib (platelet), alpha polypeptide
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所有图片(1)
About This Item
UNSPSC代码:
12352203
NACRES:
NA.41
生物来源
mouse
偶联物
unconjugated
抗体形式
purified from hybridoma cell culture
抗体产品类型
primary antibodies
克隆
PM6/40, monoclonal
表单
buffered aqueous solution
分子量
antigen ~140 kDa
种属反应性
human
浓度
~1.0 mg/mL
技术
flow cytometry: 30-60 μg/mL using human platelet
immunohistochemistry: suitable
western blot: suitable
同位素/亚型
IgG1
UniProt登记号
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... GP1BA(2811)
一般描述
Monoclonal Anti-GP1BA (mouse IgG1 isotype) is derived from the hybridoma PM6/40 produced by the fusion of mouse myeloma cells and splenocytes from immunized BALB/c mice. GP1BA, also known as glycoprotein Ib (GP Ib) and CD42b, is a platelet surface membrane glycoprotein. GP Ib is a heterodimer, composed of an α and β chain, that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the α- and β-subunits with platelet glycoprotein IX and platelet glycoprotein V. The glycoprotein Ib platelet subunit α (GP1BA) gene is mapped to human chromosome 17p13.2.
特异性
Monoclonal Anti-GP1BA recognizes human GP1BA/CD42b.
免疫原
human platelet membranes.
应用
Anti-GP1BA antibody, Mouse monoclonal is suitable for:
- immunoblotting
- fluorescence-activated cell sorting (FACS)
- immunohistochemistry
生化/生理作用
Glycoprotein Ib (GP Ib) functions as a receptor for von Willebrand factor (VWF). It regulates the adhesion of blood platelets to damaged blood vessel walls and the subsequent platelet aggregation. It also transmits signals leading to platelet activation, aggregation and secretion. 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. The interaction between Gp Ib and VWF was found to induce apoptotic events in platelets, suggesting a mechanism for platelet clearance or some thrombocytopenic disease. Furthermore, 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.
外形
0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。
储存及稳定性
For continuous use, store at 2-8°C for up to one month. For extended storage, freeze at -20oC in working aliquots. Repeated freezing and thawing,or storage in “frost-free” freezers,is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
免责声明
Unless otherwise stated in our catalog, our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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储存分类代码
10 - Combustible liquids
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Platelets
Encyclopedia of Immunology, 1973-1976 null
Alan T Nurden et al.
British journal of haematology, 165(2), 165-178 (2013-11-30)
Genetic defects of platelets constitute rare diseases that include bleeding syndromes of autosomal dominant, recessive or X-linked inheritance. They affect platelet production, resulting in a low circulating platelet count and changes in platelet morphology, platelet function, or a combination of
Indra Ramasamy
Critical reviews in oncology/hematology, 49(1), 1-35 (2004-01-22)
Platelet aggregation at sites of vascular injury is essential for the formation of the primary haemostatic plug. The mechanism of platelet aggregation under conditions of physiological flow is a complex multistep process, which requires the synergistic action of several different
Shi-Zhong Luo et al.
Journal of molecular biology, 382(2), 448-457 (2008-08-05)
As the receptor on the platelet surface for von Willebrand factor, glycoprotein (GP) Ib-IX complex is critically involved in hemostasis and thrombosis. How the complex is assembled from GP Ibalpha, GP Ib beta and GP IX subunits, all of which
Ilaria Canobbio et al.
Cellular signalling, 16(12), 1329-1344 (2004-09-24)
The glycoprotein Ib-V-IX is one of the major adhesive receptors expressed on the surface of circulating platelets. It is composed of four different polypeptides-GPIbalpha, GPIbbeta, GPIX, and GPV-and represents a multifunctional receptor able to interact with a number of ligands
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