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抗Rat (Rattus) SNAP25 抗体:
抗Mouse (Murine) SNAP25 抗体:
抗Human SNAP25 抗体:
Chicken Polyclonal SNAP25 Primary Antibody for ICC, IP - ABIN1742235
Young, Franciosi, Spreeuw, Deng, Sanders, Tam, Huang, Singaraja, Zhang, Bissada, Kay, Hayden: Low levels of human HIP14 are sufficient to rescue neuropathological, behavioural, and enzymatic defects due to loss of murine HIP14 in Hip14-/- mice. in PLoS ONE 2012
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Mouse (Murine) Monoclonal SNAP25 Primary Antibody for IF, IP - ABIN967923
Chapman, An, Barton, Jahn: SNAP-25, a t-SNARE which binds to both syntaxin and synaptobrevin via domains that may form coiled coils. in The Journal of biological chemistry 1994
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Mouse (Murine) Monoclonal SNAP25 Primary Antibody for IF, IP - ABIN967922
Hasegawa, Zinsser, Rhee, Vik-Mo, Davanger, Hay: Mammalian ykt6 is a neuronal SNARE targeted to a specialized compartment by its profilin-like amino terminal domain. in Molecular biology of the cell 2003
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Human Polyclonal SNAP25 Primary Antibody for ICC, IF - ABIN4354886
Cardoso, Ferrari, Garcia, Bregano, Andrade, Nogueira: Immunohistochemical approach to the pathogenesis of clinical cases of bovine Herpesvirus type 5 infections. in Diagnostic pathology 2010
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Human Polyclonal SNAP25 Primary Antibody for IHC (p), WB - ABIN967060
Gonelle-Gispert, Halban, Niemann, Palmer, Catsicas, Sadoul: SNAP-25a and -25b isoforms are both expressed in insulin-secreting cells and can function in insulin secretion. in The Biochemical journal 1999
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Human Polyclonal SNAP25 Primary Antibody for IHC (p), IHC - ABIN250341
Mouton-Liger, Sahún, Collin, Lopes Pereira, Masini, Thomas, Paly, Luilier, Même, Jouhault, Bennaï, Beloeil, Bizot, Hérault, Dierssen, Créau: Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: implications for Down syndrome. in Neurobiology of disease 2014
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Human Polyclonal SNAP25 Primary Antibody for IHC, ELISA - ABIN185392
Voeller: Attention-deficit hyperactivity disorder (ADHD). in Journal of child neurology 2004
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Human Polyclonal SNAP25 Primary Antibody for IHC (fro), IF (p) - ABIN738111
Wang, Wang, Liu, Zhao, Zhao, He, Qian, Xu, Liu, Liu, Liu, Liu, Zhou, Wang: SNAP25 Ameliorates Sensory Deficit in Rats with Spinal Cord Transection. in Molecular neurobiology 2014
a mouse mutant engineered to express normal levels of SNAP-25 but only SNAP-25a shows metabolic disease.
The function of synaptotagmin-1 (syt-1 (显示 SYT1 抗体)):soluble NSF attachment protein (显示 NAPG 抗体) receptor (SNARE (显示 VTI1B 抗体)) interactions during neurotransmission remains unclear.
proteins, such as syntaxin-1, Munc18-1, or SNAP-25, modulate alpha-synuclein neuropathy and/or are dysregulated in Alzheimer's disease, understanding this type of neurodegeneration may provide new links between synaptic defects and neurodegeneration in humans
Study showed that SNAP25 is synthesized in the motor nerve endings and that the level of SNAP25 mRNA affects the activity of exocytosis of the neurotransmitter
Data demonstrate a role for SNAP-25 in controlling PSD-95 (显示 DLG4 抗体) clustering and open the possibility that genetic reductions of the protein levels may contribute to the pathology through an effect on postsynaptic function and plasticity.
Data suggest that porosome-associated proteins SNAP25, TREK-1 (显示 KCNK2 抗体), syntaxin-1A (显示 STX1A 抗体), and Gai3 exhibit stability and functionality such that isolated proteins can be reconstituted as insulin (显示 INS 抗体)-secreting porosomes in cell membrane of live cells.
we demonstrate that Syb2 (显示 VAMP2 抗体) and SNAP25 mediate the vesicular release of BDNF (显示 BDNF 抗体) in axons and dendrites of cortical neurons
The extreme C terminus of SNAP25 is a critical region for the GBetaGamma-SNARE (显示 VTI1B 抗体) interaction.
Data show a significant increase of vesicle-associated membrane protein 2 (VAMP-2 (显示 VAMP2 抗体)) mRNA expression, however, the expressions of synaptosome-associated protein of 25 kDa (SNAP-25) and syntaxin 1A (显示 STX1A 抗体) did not exhibit the changes in hippocampus.
SNAP-25 phosphorylation is regulated in a stress-dependent manner through both central and peripheral mechanisms.
Findings indicate that lower SNAP-25 in ventromedial caudate in schizophrenia is primarily due to less SNAP-25A, and that the remaining SNAP-25 is associated with greater protein-protein interaction with syntaxin. The absence of a link to recent treatment effects in the human samples, or to administration of antipsychotic drugs in rats suggests the findings are illness- and not treatment-related.
Allelic variation of SNAP25 modulates development and plasticity of the prefrontal-limbic network and a shared genetic vulnerability between Bipolar Disorder and Schizophrenia.
SH3BP5 (显示 SH3BP5 抗体), LMO3 (显示 LMO3 抗体), and SNAP25 were expressed in diffuse large B-cell lymphoma cells and associated with clinical features.
show that FOXC1 (显示 FOXC1 抗体) regulates the expression of RAB3GAP1 (显示 RAB3GAP1 抗体), RAB3GAP2 (显示 RAB3GAP2 抗体) and SNAP25
study demonstrated that miR (显示 MLXIP 抗体)-27a and -b, which are widely expressed in host cells, suppress SNAP25 and TXN2 (显示 TXN2 抗体) expression through posttranscriptional gene silencing.
Data suggest that A-syn (显示 FYN 抗体) (alpha-synuclein) promotes SNARE (显示 NAPA 抗体)-dependent vesicle docking; phosphatidylserine (PS) removal from t-SNARE (显示 NAPA 抗体)-bearing vesicles causes A-syn (显示 FYN 抗体) to inhibit vesicle docking; PS removal from v-SNARE (显示 VTI1B 抗体)-bearing vesicles promotes vesicle docking; the C-terminal 45 residues of A-syn (显示 FYN 抗体) are required for promotion of vesicle docking. (Here, t-SNARE (显示 NAPA 抗体) is SNAP-25; v-SNARE (显示 VTI1B 抗体) is VAMP2 (显示 VAMP2 抗体).)
our data indicate that the expression of SNAP25 is crucial for dendrite formation and is associated with the effects of targeted chemotherapy. The detection of SNAP25 expression in MB cells may thus be essential for the chemotherapeutic application of Ara (显示 FOXC1 抗体)-C.
Robust association of the rs3746544 SNP and ASD (显示 ARSD 抗体), in both allele and haplotype-based analyses, was observed in Iranian population.
Our results will provide novel evidence to reveal the possible role of SNAP-25 in B[a]P-induced neurotoxicity and may be helpful for searching the potential strategy for the prevention measures against B[a]P neurotoxicity.
Our analysis indicated that there is no significant association between none of studied variants in SNAP-25 and ADHD.
In individual chromaffin cells, we tracked conformational changes in SNAP25 by total internal reflection fluorescence resonance energy transfer (FRET) microscopy while exocytotic catecholamine release from single vesicles was simultaneously recorded
dynamic experiments using TIRFM revealed that attenuation of cortical F-actin movement clearly diminishes the mobility of SNAP-25 clusters.
Stable syntaxin/SNAP-25 dimers are a central principle of the SNARE (显示 NAPA 抗体) assembly pathway underlying regulated exocytosis.
microdomains carrying syntaxin1 (显示 STX1A 抗体)/SNAP-25 and different types of calcium channels act as the sites for physiological granule fusion in "in situ" chromaffin cells
These data demonstrate a differential ability of SNAP-25 homlog to support neuronal function.
data indicate that SNARE (显示 NAPA 抗体) proteins VAMP-2 (显示 VAMP2 抗体) and SNAP-25 play an essential role in daughter blastomere apposition, possibly via the delivery of components that promote the cell-to-cell adhesion required for the successful completion of cytokinesis
Synaptic vesicle membrane docking and fusion is mediated by SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) located on the vesicle membrane (v-SNAREs) and the target membrane (t-SNAREs). The assembled v-SNARE/t-SNARE complex consists of a bundle of four helices, one of which is supplied by v-SNARE and the other three by t-SNARE. For t-SNAREs on the plasma membrane, the protein syntaxin supplies one helix and the protein encoded by this gene contributes the other two. Therefore, this gene product is a presynaptic plasma membrane protein involved in the regulation of neurotransmitter release. Two alternative transcript variants encoding different protein isoforms have been described for this gene.
synaptosomal-associated protein 25
, super protein
, synaptosomal-associated 25 kDa protein
, synaptosomal-associated protein, 25 kDa
, GENA 70
, blind drunk
, resistance to inhibitors of cholinesterase 4 homolog
, synaptosomal associated protein-25
, synaptosomal-associated protein 25 isoform SNAP25B
, synaptosomal-associated 25kD protein