GP9 Rabbit Polyclonal Antibody (CAB5374)
- SKU:
- CAB5374
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cardiovascular
Frequently bought together:
Description
Product Name: | GP9 Rabbit Polyclonal Antibody |
SKU: | CAB5374 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 17-147 of human GP9 (NP_000165.1). |
Sequence: | TKDC PSPC TCRA LETM GLWV DCRG HGLT ALPA LPAR TRHL LLAN NSLQ SVPP GAFD HLPQ LQTL DVTQ NPWH CDCS LTYL RLWL EDRT PEAL LQVR CASP SLAA HGPL GRLT GYQL GSCG WQLQ ASWV RPG |
Tested Applications: | WB IHC-P ELISA |
Recommended Dilution: | WB,1:100 - 1:500 IHC-P,1:50 - 1:200 |
Synonyms: | GPIX; CD42a; GP9 |
Positive Sample: | K-562 |
Conjugate: | Unconjugated |
Cellular Localization: | Membrane, Single-pass type I membrane protein. |
Calculated MW: | 19kDa |
Observed MW: | 19kDa |
This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency.
Purification Method: | Affinity purification |
Gene ID: | 2815 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3. |