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Merck

SAB4200247

Sigma-Aldrich

Anti-GP1BA antibody, Mouse monoclonal

clone PM6/40, purified from hybridoma cell culture

Sinónimos:

MonoclonalAnti-BSS, MonoclonalAnti-CD42B, MonoclonalAnti-CD42balpha, MonoclonalAnti-GP1B, MonoclonalAnti-MGC34595, MonoclonalAnti-glycoprotein Ib (platelet), alpha polypeptide

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

origen biológico

mouse

conjugado

unconjugated

forma del anticuerpo

purified from hybridoma cell culture

tipo de anticuerpo

primary antibodies

clon

PM6/40, monoclonal

Formulario

buffered aqueous solution

mol peso

antigen ~140 kDa

reactividad de especies

human

concentración

~1.0 mg/mL

técnicas

flow cytometry: 30-60 μg/mL using human platelet
immunohistochemistry: suitable
western blot: suitable

isotipo

IgG1

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... GP1BA(2811)

Descripción general

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.

Especificidad

Monoclonal Anti-GP1BA recognizes human GP1BA/CD42b.

Inmunógeno

human platelet membranes.

Aplicación

Anti-GP1BA antibody, Mouse monoclonal is suitable for:
  • immunoblotting
  • fluorescence-activated cell sorting (FACS)
  • immunohistochemistry

Acciones bioquímicas o fisiológicas

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.

Forma física

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Almacenamiento y estabilidad

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.

Cláusula de descargo de responsabilidad

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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Código de clase de almacenamiento

10 - Combustible liquids

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Visite la Librería de documentos

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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