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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 Proteins (21) and many more products for this protein.
Showing 10 out of 76 products:
Human Polyclonal VAMP7 Primary Antibody for IHC, WB - ABIN351364
DEsposito, Ciccodicola, Gianfrancesco, Esposito, Flagiello, Mazzarella, Schlessinger, DUrso: A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation. in Nature genetics 1996
Show all 7 references for ABIN351364
Human Polyclonal VAMP7 Primary Antibody for IHC (p), WB - ABIN657786
Vivona, Liu, Strop, Rossi, Filippini, Brunger: The longin SNARE VAMP7/TI-VAMP adopts a closed conformation. in The Journal of biological chemistry 2010
Show all 3 references for ABIN657786
Rat (Rattus) Monoclonal VAMP7 Primary Antibody for IHC, WB - ABIN1742477
Muzerelle, Alberts, Martinez-Arca, Jeannequin, Lafaye, Mazié, Galli, Gaspar: Tetanus neurotoxin-insensitive vesicle-associated membrane protein localizes to a presynaptic membrane compartment in selected terminal subsets of the rat brain. in Neuroscience 2003
Show all 3 references for ABIN1742477
Human Monoclonal VAMP7 Primary Antibody for ICC, IF - ABIN1724622
Feldmann, Amphornrat, Scha?nherr, Winterstein, Ma?bius, Ruhwedel, Danglot, Nave, Galli, Bruns, Trotter, Kra?mer-Albers: Transport of the major myelin proteolipid protein is directed by VAMP3 and VAMP7. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
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GLUT5 (show SLC2A5 Antibodies) required an interaction cascade of Rab11 (show RAB11A Antibodies), Myo5B, Slp4a, Munc18-2 (show STXBP2 Antibodies), and Vamp7 with Stx3 (show STX3 Antibodies).
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 Antibodies) and VAMP7 play in selection of the pathways leading to generation of ultrastructurally different LC3 (show MAP1LC3A Antibodies) compartments
Increased level of SNAP23 (show SNAP23 Antibodies)-Syntaxin4 (show STX4 Antibodies)-VAMP7 interaction correlates with decreased Syntaxin4 (show STX4 Antibodies) phosphorylation and trafficking of MT1-MMP (show MMP14 Antibodies) to invadopodia during cellular invasion.
increased gene dosage of VAMP7, and thus higher expression levels of its protein product, enhances estrogen receptor (show ESR1 Antibodies) 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 Antibodies) 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 Antibodies))-positive vacuoles colocalize with LC3 (show MAP1LC3A Antibodies) at the cell periphery (focal adhesions) upon starvation.
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 Antibodies). VAMP7-deficient mice exhibit reduced functional expression of TRPM8 (show TRPM8 Antibodies) 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 Antibodies) and vesicle-associated membrane protein 1 (show VAMP1 Antibodies) are more suitable targets to abolish functional soluble N-ethylmaleimide-sensitive factor attachment protein receptor (show VTI1B Antibodies) complexes
VAMP7 controls the phosphorylation of Lat (show LAT Antibodies), formation of the TCR-Lat (show LAT Antibodies) signaling complex and, ultimately, activation of T cells.
The binding of VAMP7 to delta-adaptin (show AP3D1 Antibodies) requires the VAMP7 SNARE (show VTI1B Antibodies) motif to be engaged in SNARE (show VTI1B Antibodies) complex formation and hence AP3 (show AP3B1 Antibodies) must transport VAMP7 when VAMP7 is part of a cis (show CISH Antibodies)-SNARE (show VTI1B Antibodies) 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 (show SLC17A7 Antibodies) and VAMP2 (show VAMP2 Antibodies) in the recycling pool and of VAMP7 in the resting pool
VAMP7 controls exocytosis of proteolipid protein (myelin) 1 (show PLP1 Antibodies) from late endosomal/lysosomal organelles as part of a transcytosis pathway
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