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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. Zusätzlich bieten wir Ihnen VAMP7 Proteine (13) und und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 76 products:
Rat (Rattus) Monoclonal VAMP7 Primary Antibody für 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 Pubmed References
Human Monoclonal VAMP7 Primary Antibody für 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
Show all 2 Pubmed References
Dog (Canine) Monoclonal VAMP7 Primary Antibody für ELISA, ICC - ABIN446491
Spessott, Sanmillan, Kulkarni, McCormick, Giraudo: Syntaxin 4 mediates endosome recycling for lytic granule exocytosis in cytotoxic T-lymphocytes. in Traffic (Copenhagen, Denmark) 2018
Human Polyclonal VAMP7 Primary Antibody für ICC, IF - ABIN4364782
Tannour-Louet, Han, Louet, Zhang, Romero, Addai, Sahin, Cheung, Lamb: Increased gene copy number of VAMP7 disrupts human male urogenital development through altered estrogen action. in Nature medicine 2014
GLUT5 (zeige SLC2A5 Antikörper) required an interaction cascade of Rab11 (zeige RAB11A Antikörper), Myo5B, Slp4a, Munc18-2 (zeige STXBP2 Antikörper), and Vamp7 with Stx3 (zeige STX3 Antikörper).
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 (zeige VAMP3 Antikörper) and VAMP7 play in selection of the pathways leading to generation of ultrastructurally different LC3 (zeige MAP1LC3A Antikörper) compartments
Increased level of SNAP23 (zeige SNAP23 Antikörper)-Syntaxin4 (zeige STX4 Antikörper)-VAMP7 interaction correlates with decreased Syntaxin4 (zeige STX4 Antikörper) phosphorylation and trafficking of MT1-MMP (zeige MMP14 Antikörper) to invadopodia during cellular invasion.
increased gene dosage of VAMP7, and thus higher expression levels of its protein product, enhances estrogen receptor (zeige ESR1 Antikörper) 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 (zeige VPS41 Antikörper) 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 (zeige VTI1B Antikörper))-positive vacuoles colocalize with LC3 (zeige MAP1LC3A Antikörper) 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 (zeige TRPM8 Antikörper). VAMP7-deficient mice exhibit reduced functional expression of TRPM8 (zeige TRPM8 Antikörper) 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 (zeige STX1A Antikörper) and vesicle-associated membrane protein 1 (zeige VAMP1 Antikörper) are more suitable targets to abolish functional soluble N-ethylmaleimide-sensitive factor attachment protein receptor (zeige VTI1B Antikörper) complexes
VAMP7 controls the phosphorylation of Lat (zeige LAT Antikörper), formation of the TCR-Lat (zeige LAT Antikörper) signaling complex and, ultimately, activation of T cells.
The binding of VAMP7 to delta-adaptin (zeige AP3D1 Antikörper) requires the VAMP7 SNARE (zeige VTI1B Antikörper) motif to be engaged in SNARE (zeige VTI1B Antikörper) complex formation and hence AP3 (zeige AP3B1 Antikörper) must transport VAMP7 when VAMP7 is part of a cis (zeige CISH Antikörper)-SNARE (zeige VTI1B Antikörper) 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 (zeige VAMP2 Antikörper) 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