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VAMP7 encodes a transmembrane protein that is a member of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) family. Additionally we are shipping VAMP7 Antibodies (72) and many more products for this protein.
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GLUT5 required an interaction cascade of Rab11 (show RAB11A Proteins), Myo5B, Slp4a, Munc18-2 (show STXBP2 Proteins), and Vamp7 with Stx3 (show STX3 Proteins).
VAMP-7 participates in both platelet granule secretion and spreading and suggest a mechanism whereby VAMP-7 links granule exocytosis with actin reorganization.
highlight the role that VAMP3 (show VAMP3 Proteins) and VAMP7 play in selection of the pathways leading to generation of ultrastructurally different LC3 (show MAP1LC3A Proteins) compartments
Increased level of SNAP23 (show SNAP23 Proteins)-Syntaxin4 (show STX4 Proteins)-VAMP7 interaction correlates with decreased Syntaxin4 (show STX4 Proteins) phosphorylation and trafficking of MT1-MMP (show MMP14 Proteins) to invadopodia during cellular invasion.
increased gene dosage of VAMP7, and thus higher expression levels of its protein product, enhances estrogen receptor (show ESR1 Proteins) action in male genitourinary tissues
CALM is able to sort VAMP4 and VAMP7, even though they have sorting signals for other clathrin adaptors.
Overexpression of Vamp7 inhibited the heterotypic fusion with lysosomes and the homotypic fusion between individual Coxiella phagosomes and replicative vacuoles.
Activation of TI-VAMP-mediated exocytosis thus relies on tyrosine phosphorylation.
hVps41 (show VPS41 Proteins) and VAMP7 are specifically involved in the fusion of trans-Golgi network-derived lysosome-associated membrane protein carriers with late endosomes.
In a mammalian tumor cell line a subset of VAMP7 (V-SNARE (show VTI1B Proteins))-positive vacuoles colocalize with LC3 (show MAP1LC3A Proteins) at the cell periphery (focal adhesions) upon starvation.
VAMP7 mediates fusion of BLOC-1-dependent transport carriers with melanosomes, illuminate SNARE recycling from melanosomes as a critical BLOC-3-dependent step.
VAMP7-mediated release of interleukin-12 at the immune synapse is a mechanism to transmit innate signals to T cells.
VAMP7 mediates plasma membrane fusion of vesicles containing TRPM8 (show TRPM8 Proteins). VAMP7-deficient mice exhibit reduced functional expression of TRPM8 (show TRPM8 Proteins) in sensory neurons and concomitant deficits in cold avoidance and icilin-induced cold hypersensitivity.
VAMP-7(-/-) platelets demonstrated a partial defect in dense granule exocytosis and impaired aggregation. Consistent with a role in cytoskeletal remodeling, spreading on matrices was decreased in VAMP-7(-/-) platelets compared to wild-type controls.
syntaxin 1 (show STX1A Proteins) and vesicle-associated membrane protein 1 (show VAMP1 Proteins) are more suitable targets to abolish functional soluble N-ethylmaleimide-sensitive factor attachment protein receptor (show VTI1B Proteins) complexes
VAMP7 controls the phosphorylation of Lat (show LAT Proteins), formation of the TCR-Lat (show LAT Proteins) signaling complex and, ultimately, activation of T cells.
The binding of VAMP7 to delta-adaptin requires the VAMP7 SNARE (show VTI1B Proteins) motif to be engaged in SNARE (show VTI1B Proteins) complex formation and hence AP3 (show AP3B1 Proteins) must transport VAMP7 when VAMP7 is part of a cis (show CISH Proteins)-SNARE (show VTI1B Proteins) complex.
Behavioral characterization studies indicate that deletion of Vamp7 exon 7 is associated with increased anxiety in mice.
VAMP7 is required in neurons to extend axons to the full extent. VAMP7 does not seem to be required for epithelial cell polarity and lysosomal exocytosis.
VAMP7, and other synaptic vesicle proteins thus target to both recycling and resting pools. However, the proportions differ dramatically, with higher levels of VGLUT1 and VAMP2 (show VAMP2 Proteins) in the recycling pool and of VAMP7 in the resting pool
This gene encodes a transmembrane protein that is a member of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) family. The encoded protein localizes to late endosomes and lysosomes and is involved in the fusion of transport vesicles to their target membranes. Alternate splicing results in multiple transcript variants.
vesicle-associated membrane protein 7
, synaptobrevin-like 1
, synaptobrevin-like protein 1
, tetanus neurotoxin-insensitive VAMP
, tetanus-insensitive VAMP
, synaptobrevin like 1
, tetanus neurotoxin-insensitive vesicle-associated membrane protein