Recombinant Anti-GP1BA Vesicular Antibody, EV Displayed (VS-0425-YC574)
CAT#: VS-0425-YC574
The Recombinant Anti-GP1BA Vesicular Antibody, EV Displayed (VS-0425-YC574) is an antibody-displaying extracellular vesicle (Ab-EV). The product combines the benefits of both extracellular vesicle (EV) and antibody (Ab) which can guide the decorated EVs to GP1BA-expressed cells or tissues. GP1BA is the alpha subunit of glycoprotein Ib, a receptor for von Willebrand factor (VWF) involved in platelet adhesion to vascular injury sites. Mutations in this gene cause Bernard-Soulier syndromes and platelet-type von Willebrand disease.


Recombinant Antibody
- Application
- ELISA, FC, Inhib, Cell-uptake
- Product Type
- Ab-Fc-EVs
- Antibody Quantification (Ab/EV)
- ~100 Ab/EV
- Target
- GP1BA
- Host Animal
- Mouse
- Antibody Isotype
- IgG
- Species Reactivity
- Human
- Expression Cell
- Mammalian cell
Engineered EVs
- EV-sorting domain
- CD63
- Fc-binding domain
- Protein A
- EV Size
- 30~150 nm
- Producing Cell
- HEK293F
- Isolation Method
- Gradient centrifugation
- Purification
- qEV size exclusion chromatography
- Concentration
- 1 x 10¹⁰
- Size
- 1 mL
- Buffer
- PBS
- Storage
- Store at -80°C for 12 months
Target
- Full Name
- Glycoprotein Ib platelet subunit alpha
- Biological Process
- Blood coagulation, Cell adhesion, Hemostasis
- Introduction
- 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.
- Alternative Names
- CD42b, GP1B, GPIbalpha
- Gene ID
- 2811
- UniProt ID
- P07359
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Datasheet
MSDS
COA
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