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GP6 encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. Zusätzlich bieten wir Ihnen GP6 Kits (31) und GP6 Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.
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Platelet adhesion to collagen induces GPVI dimer clustering. GPVI clustering increases both avidity for collagen and the proximity of GPVI-associated signaling molecules, which may be crucial for the initiation and persistence of signaling
Loss of the platelet surface receptors GPIbalpha (zeige GP1BA Antikörper) and GPVI in heart failure, CF-VAD (zeige KCTD1 Antikörper) and ECMO patients may contribute to ablated platelet adhesion/activation, and limit thrombus formation under high/pathologic shear conditions
Novel antithrombotic peptides derived from trowaglerix that acts through GPVI antagonism with greater safety-no severe bleeding.
results support the idea that genetic variability of GP6 regulatory regions can be associated with platelet hyperaggregability - a possible cause of miscarriage
These results demonstrate that GP6 is a receptor for fibrin and provide evidence that this interaction contributes to thrombus growth and stability.
data suggest a novel role for FAK (zeige PTK2 Antikörper) in GPVI-dependent ROS (zeige ROS1 Antikörper) formation and platelet activation and elucidate a proximal signaling role for FAK (zeige PTK2 Antikörper) within the GPVI pathway.
This study identifies GPVI as a platelet receptor for polymerized fibrin with 2 major functions: (1) amplification of thrombin (zeige F2 Antikörper) generation and (2) recruitment of circulating platelets to clots.
Glaucocalyxin A inhibits platelet activation and thrombus formation preferentially via GPVI signaling pathway.
The plasma levels of sGPVI were the highest in patients with TMA without markedly reduced ADAMTS13 (zeige ADAMTS13 Antikörper) and those were significantly reduced after plasma exchange.
Results suggest that variants of GP6 SNPs, namely, rs1671153, rs1654410, rs1654419, and rs1613662, may be associated with risk of recurrent miscarriage.
These results reveal a novel and unexpected function of hepatic Fc-gamma-RIIB in the targeted downregulation of GPVI in vivo.
collagen-I-mediated inhibition of proplatelet formation is specifically controlled by GPVI.
platelet GP6 and thromboxane A2 receptor (zeige TBXA2R Antikörper) have a role in promoting inflammatory macrophage phenotype in skin inflammation
TULA-2 (zeige STS1 Antikörper) Protein Phosphatase Suppresses Activation of Syk (zeige SYK Antikörper) through the GPVI Platelet Receptor for Collagen by Dephosphorylating Tyr (zeige TYR Antikörper)(P)346, a Regulatory Site of Syk (zeige SYK Antikörper).
Inhibition of platelet activation by an anti-GPVI antibody significantly reduces infarct size.
These results demonstrate that GPVI is a receptor for fibrin and provide evidence that this interaction contributes to thrombus growth and stability.
data demonstrate that genetic deletion of GPVI receptor, FcRgamma (zeige FCER1G Antikörper) chain, or the alpha2beta1 integrin changes the thrombotic potentials of these platelets to collagen dependent on the stimulus mechanism.
our results show that GPVI plays a dual role in inflammation by enhancing neutrophil-damaging activities while supporting the activation and hemostatic adhesion of single platelets to neutrophil-induced vascular breaches.
This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
, platelet collagen receptor
, platelet glycoprotein VI
, glycoprotein VI (platelet)
, glycoprotein 5
, glycoprotein 6 (platelet)
, glycoprotein VI