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.

(Hematopoietic cells
Staining: Medium
Intensity: Strong
Quantity: <25%
Location: Cytoplasmic/membranous)
* Image credit: Human Protein Atlas v21.proteinatlas.org/images/2496/6301_B_6_4.jpg

(Cell lines ordered by descending RNA expression order.)
* Image credit: Human Protein Atlas v21.proteinatlas.org/ENSG00000185245-GP1BA
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
Downloads
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See other products for "GP1BA"
Select a product category from the dropdown menu below to view related products.
CAT | Product Name | Application | Type |
---|---|---|---|
MOB-413 | Recombinant Anti-human GP1BA Antibody | ELISA, WB, Neut, FuncS | IgG |
MRO-1754-CN | Rabbit Anti-GP1BA Polyclonal Antibody (MRO-1754-CN) | WB, IF, IHC, FC | Rabbit IgG |
FN-141CQ | Human Anti-GP1BA Recombinant Antibody (clone CBL-1310) | FuncS, Block | Human IgG1 |
HPAB-0367-YJ | Mouse Anti-GP1BA Recombinant Antibody (HPAB-0367-YJ) | ELISA, FC, WB, Inhib | Mouse IgG |
VS2-QX5 | Mouse Anti-GP1BA Recombinant Antibody (clone PAB-5) | IF | Mouse IgG1, κ |
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For Research Use Only. Not For Clinical Use.
For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.
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