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VAMP8 encodes an integral membrane protein that belongs to the synaptobrevin/vesicle-associated membrane protein subfamily of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs). Additionally we are shipping VAMP8 Antibodies (38) and VAMP8 Proteins (9) and many more products for this protein.
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our study suggested that VAMP8 gene variants might not contribute to glioma susceptibility and associated with glioma in the Chinese Han population.
Vesicle-associated membrane protein 8 as a novel oncogene (show RAB1A ELISA Kits) by promoting cell proliferation and therapeutic resistance in glioma. Targeting VAMP8 may serve as a potential therapeutic regimen for the treatment of glioma.
Starvation-induced MTMR13 (show SBF2 ELISA Kits) and RAB21 (show RAB21 ELISA Kits) activity regulates VAMP8 to promote autophagosome-lysosome fusion.
Cytotoxic granule exocytosis is a sequential, multivesicle fusion process requiring VAMP8-mediated recycling endosome fusion before cytotoxic granule fusion.
Inhibition of VAMP8, but not VAMP7 (show VAMP7 ELISA Kits), significantly reduces viral entry.
VAMP8 regulates mucin (show SLC13A2 ELISA Kits) granule exocytosis in airway goblet cells, and reduction of its expression may provide a novel therapeutic target to ameliorate airway mucus obstruction in lung diseases
Assessment of KIF6 genotype is not useful in predicting low density lipoprotein cholesterol lowering response to pravastatin, and heart disease risk reduction in the elderly.
Dynamics of FIP3 (show IKBKG ELISA Kits)- and VAMP8-containing endosomes reflect the progressive stages of abscission.
The VAMP8 rs1010 polymorphism was associated with CHD risk in Chinese Han population, the A allele might serve as a genetic risk factor of coronary heart disease.
Results suggest that the combinational SNARE proteins VAMP8 and Vti1b mediate the fusion of antimicrobial and canonical autophagosomes with lysosomes, an essential event for autophagic degradation.
VAMP8-mediated secretion is dependent on anterograde endosomal trafficking.
Leishmania evades host immunity by GP63 (show LMLN ELISA Kits)-mediated VAMP8 cleavage.
VAMP8 mediates insulin (show INS ELISA Kits) granule recruitment to the plasma membrane, which partly accounts for GLP-1 (show GCG ELISA Kits) potentiation of glucose-stimulated insulin (show INS ELISA Kits) secretion.
VAMP8 knockout mice were used to show that the SNARE (show VTI1B ELISA Kits) machinery plays a critical role in the process of granule homotypic fusion.
that granule-to-granule fusion is regulated by VAMP8 containing SNARE (show VTI1B ELISA Kits) complexes distinct from those that regulate primary granule fusion.
data demonstrate that, in the absence of VAMP8, the relative subcellular distribution of GLUT4 (show SLC2A4 ELISA Kits) is altered, resulting in increased sarcolemma levels that can account for increased glucose clearance and insulin (show INS ELISA Kits) sensitivity
VAMP8 mediates the regulated fusion of AQP2 (show AQP2 ELISA Kits)-positive vesicles with the plasma membrane.
VAMP8 has a role in regulated exocytosis of pancreatic acinar cells by serving as a v-SNARE (show GOSR1 ELISA Kits) of zymogen granules
VAMP-8 is required for release from dense core granules, alpha granules, and lysosomes.
This gene encodes an integral membrane protein that belongs to the synaptobrevin/vesicle-associated membrane protein subfamily of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs). The encoded protein is involved in the fusion of synaptic vesicles with the presynaptic membrane.
vesicle-associated membrane protein 8
, vesicle-associated membrane protein 8 (endobrevin)
, Vesicle-associated membrane protein 8