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Specificity of vesicular transport is regulated, in part, by the interaction of a vesicle-associated membrane protein termed synaptobrevin/VAMP with a target compartment membrane protein termed syntaxin. De plus, nous expédions Synaptosomal-Associated Protein, 23kDa Protéines (13) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal SNAP23 Primary Antibody pour ICC, IF - ABIN4354884
Stadler, Hjelmare, Neumann, Jonasson, Pepperkok, Uhlén, Lundberg: Systematic validation of antibody binding and protein subcellular localization using siRNA and confocal microscopy. dans Journal of proteomics 2012
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Human Polyclonal SNAP23 Primary Antibody pour ELISA, WB - ABIN4354882
Gratacòs, Costas, de Cid, Bayés, González, Baca-García, de Diego, Fernández-Aranda, Fernández-Piqueras, Guitart, Martín-Santos, Martorell, Menchón, Roca, Sáiz-Ruiz, Sanjuán, Torrens, Urretavizcaya et al.: Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and ... dans American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009
Human Polyclonal SNAP23 Primary Antibody pour ELISA, WB - ABIN4354883
Boström, Andersson, Vind, Håversen, Rutberg, Wickström, Larsson, Jansson, Svensson, Brånemark, Ling, Beck-Nielsen, Borén, Højlund, Olofsson: The SNARE protein SNAP23 and the SNARE-interacting protein Munc18c in human skeletal muscle are implicated in insulin resistance/type 2 diabetes. dans Diabetes 2010
Human Polyclonal SNAP23 Primary Antibody pour IF, IHC - ABIN347010
Galli, Zahraoui, Vaidyanathan, Raposo, Tian, Karin, Niemann, Louvard: A novel tetanus neurotoxin-insensitive vesicle-associated membrane protein in SNARE complexes of the apical plasma membrane of epithelial cells. dans Molecular biology of the cell 1998
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Rat (Rattus) Polyclonal SNAP23 Primary Antibody pour IP, WB - ABIN1742238
Tadokoro, Shibata, Inoh, Amano, Nakanishi, Hirashima, Utsunomiya-Tate: Phosphorylation of syntaxin-3 at Thr 14 negatively regulates exocytosis in RBL-2H3 mast cells. dans Cell biology international 2016
These results demonstrate opposing roles for SNAP23 in the secretion mechanisms of the endocrine and exocrine pancreas.
SNAP23 is selectively expressed in airway secretory cells and mediates baseline and stimulated mucin (Montrer SLC13A2 Anticorps) secretion.
these data suggest that SNAP23 is a key component of the endothelial SNARE (Montrer VTI1B Anticorps) machinery that mediates endothelial exocytosis.
Data indicate that acute depletion of synaptosomal-associated protein 23 (SNAP-23) in fibroblasts leads to rapid apoptotic cell death.
Use of neurons from double-knock-out (SNAP-25 (Montrer SNAP25 Anticorps), synaptotagmin-7 (Montrer SYT7 Anticorps)) mice in combination with viral transduction showed that SNAP-23-driven release is triggered by endogenous synaptotagmin-7 (Montrer SYT7 Anticorps)
Results suggest that Plin2 (Montrer PLIN2 Anticorps) inhibits glucose uptake by interacting with, and regulating cellular targeting of SNAP23 to lipid droplets.
morphine suppresses TLR4 (Montrer TLR4 Anticorps)-induced TNF (Montrer TNF Anticorps) release in mast cells, preventing the IKK (Montrer CHUK Anticorps)-dependent phosphorylation of SNAP-23, which is necessary for TNF (Montrer TNF Anticorps) exocytosis, and this inhibition correlates with the formation of a beta (Montrer SUCLA2 Anticorps)-arrestin-2 (Montrer ARRB2 Anticorps)/TRAF6 (Montrer TRAF6 Anticorps) complex
We report the regulation of platelet secretion via phosphorylation of SNAP-23 at Ser95.
Results suggest that phagosomal SNAP-23 is one of the key players regulating the phagosomal environment in macrophages.
We concluded that the SNARE (Montrer VTI1B Anticorps) protein SNAP23 mediates cAMP-stimulated renin (Montrer REN Anticorps) release.
A novel regulatory mechanism for SNAP23-dependent mast cell activation of T. vaginalis-secreted LTB4 involving surface trafficking of BLT1.
Study identified SNAP23 as a novel oncogene (Montrer RAB1A Anticorps) in Ovarian Cancer (OC). It is over-expressed in OC and could promote the proliferation, migration and invasion of OC in vitro.
Localization of SNAP23 was found in plasma membrane, lipid droplets and mitochondria of skeletal muscle.
these data suggest that SNAP23 is a key component of the endothelial SNARE (Montrer NAPA Anticorps) machinery that mediates endothelial exocytosis.
Increased level of SNAP23-Syntaxin4 (Montrer STX4 Anticorps)-VAMP7 (Montrer VAMP7 Anticorps) interaction correlates with decreased Syntaxin4 (Montrer STX4 Anticorps) phosphorylation and trafficking of MT1-MMP (Montrer MMP14 Anticorps) to invadopodia during cellular invasion.
The association of Src (Montrer SRC Anticorps), EGFR (Montrer EGFR Anticorps) and beta1 integrin is dependent upon membrane traffic that is mediated by syntaxin13 (officially known as STX12 (Montrer STX12 Anticorps)) and SNAP23.
Data suggest SNAP23 and VAMP3 (vesicle-associated membrane protein 3 (Montrer VAMP3 Anticorps)) participate in interleukin-1beta-, interleukin-1 receptor-, calcium signaling-dependent secretion/exocytosis of interleukin-6 (Montrer IL6 Anticorps) and tumor necrosis factor alpha (Montrer TNF Anticorps) from synoviocytes.
STX-3 (Montrer STX3 Anticorps) and SNAP-23 are crucial for the release of all chemokines in mature human mast cells
Data show that knockdown of SNAP-23 inhibited the production of virus.
mRNA levels of BSCL2 (Montrer BSCL2 Anticorps) and SNAP23, but not COPA (Montrer COPA Anticorps), increased during adipocyte differentiation. Redistribution of SNAP23 protein to different cellular compartments was observed when comparing undifferentiated mesenchymal stem cells and differentiated adipocytes.
Specificity of vesicular transport is regulated, in part, by the interaction of a vesicle-associated membrane protein termed synaptobrevin/VAMP with a target compartment membrane protein termed syntaxin. These proteins, together with SNAP25 (synaptosome-associated protein of 25 kDa), form a complex which serves as a binding site for the general membrane fusion machinery. Synaptobrevin/VAMP and syntaxin are believed to be involved in vesicular transport in most, if not all cells, while SNAP25 is present almost exclusively in the brain, suggesting that a ubiquitously expressed homolog of SNAP25 exists to facilitate transport vesicle/target membrane fusion in other tissues. The protein encoded by this gene is structurally and functionally similar to SNAP25 and binds tightly to multiple syntaxins and synaptobrevins/VAMPs. It is an essential component of the high affinity receptor for the general membrane fusion machinery and is an important regulator of transport vesicle docking and fusion. Two alternative transcript variants encoding different protein isoforms have been described for this gene.
synaptosomal-associated protein 23
, synaptosomal-associated protein 23 isoform SNAP23A
, synaptosomal-associated protein, 23kDa
, synaptosomal-associated protein, 23kD
, vesicle-membrane fusion protein SNAP-23
, synaptosomal-associated protein 23 kD
, synaptosomal-associated protein, 23 kD