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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). Zusätzlich bieten wir Ihnen VAMP8 Antikörper (42) und VAMP8 Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
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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 (zeige RAB1A Proteine) 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 and RAB21 (zeige RAB21 Proteine) 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 (zeige VAMP7 Proteine), significantly reduces viral entry.
VAMP8 regulates mucin (zeige SLC13A2 Proteine) 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 (zeige IKBKG Proteine)- 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.
acute inhibition of VAMP8-mediated secretion during pancreatitis triggers intracellular trypsin accumulation and loss of the early endosomal compartment
These findings reveal a role for VAMP8 in LC3 (zeige MAP1LC3A Proteine)-associated phagocytosis and highlight a novel mechanism exploited by L. major promastigotes to interfere with the host antimicrobial machinery
VAMP8-mediated secretion is dependent on anterograde endosomal trafficking.
Leishmania evades host immunity by GP63 (zeige LMLN Proteine)-mediated VAMP8 cleavage.
VAMP8 mediates insulin (zeige INS Proteine) granule recruitment to the plasma membrane, which partly accounts for GLP-1 (zeige GCG Proteine) potentiation of glucose-stimulated insulin (zeige INS Proteine) secretion.
VAMP8 knockout mice were used to show that the SNARE (zeige VTI1B Proteine) machinery plays a critical role in the process of granule homotypic fusion.
that granule-to-granule fusion is regulated by VAMP8 containing SNARE (zeige VTI1B Proteine) complexes distinct from those that regulate primary granule fusion.
data demonstrate that, in the absence of VAMP8, the relative subcellular distribution of GLUT4 (zeige SLC2A4 Proteine) is altered, resulting in increased sarcolemma levels that can account for increased glucose clearance and insulin (zeige INS Proteine) sensitivity
VAMP8 mediates the regulated fusion of AQP2 (zeige AQP2 Proteine)-positive vesicles with the plasma membrane.
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