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Human SNAP25 Protein expressed in HEK-293 Cells - ABIN2732308
Brinkmalm, Brinkmalm, Honer, Moreno, Jakobsson, Mallucci, Zetterberg, Blennow, Öhrfelt: Targeting synaptic pathology with a novel affinity mass spectrometry approach. in Molecular & cellular proteomics : MCP 2014
Show all 2 Pubmed References
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 (show SYT1 Proteins)):soluble NSF attachment protein (show NAPG Proteins) receptor (SNARE (show VTI1B Proteins)) 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 (show DLG4 Proteins) 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 (show KCNK2 Proteins), syntaxin-1A (show STX1A Proteins), and Gai3 exhibit stability and functionality such that isolated proteins can be reconstituted as insulin (show INS Proteins)-secreting porosomes in cell membrane of live cells.
we demonstrate that Syb2 (show VAMP2 Proteins) and SNAP25 mediate the vesicular release of BDNF (show BDNF Proteins) in axons and dendrites of cortical neurons
The extreme C terminus of SNAP25 is a critical region for the GBetaGamma-SNARE (show VTI1B Proteins) interaction.
Reduction of SNAP-25 levels in adolescent mice was associated with hyperactivity, cognitive and social impairment and an abnormal EEG, characterized by the occurrence of frequent spikes.
Data show a significant increase of vesicle-associated membrane protein 2 (VAMP-2 (show VAMP2 Proteins)) mRNA expression, however, the expressions of synaptosome-associated protein of 25 kDa (SNAP-25) and syntaxin 1A (show STX1A Proteins) did not exhibit the changes in hippocampus.
Single nucleotide polymorphism in SNAP-25 gene is associated with Attention deficit hyperactivity disorder.
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 (show SH3BP5 Proteins), LMO3 (show LMO3 Proteins), and SNAP25 were expressed in diffuse large B-cell lymphoma cells and associated with clinical features.
show that FOXC1 (show FOXC1 Proteins) regulates the expression of RAB3GAP1 (show RAB3GAP1 Proteins), RAB3GAP2 and SNAP25
study demonstrated that miR (show MLXIP Proteins)-27a and -b, which are widely expressed in host cells, suppress SNAP25 and TXN2 (show TXN2 Proteins) expression through posttranscriptional gene silencing.
Data suggest that A-syn (show FYN Proteins) (alpha-synuclein) promotes SNARE (show NAPA Proteins)-dependent vesicle docking; phosphatidylserine (PS) removal from t-SNARE (show NAPA Proteins)-bearing vesicles causes A-syn (show FYN Proteins) to inhibit vesicle docking; PS removal from v-SNARE (show VTI1B Proteins)-bearing vesicles promotes vesicle docking; the C-terminal 45 residues of A-syn (show FYN Proteins) are required for promotion of vesicle docking. (Here, t-SNARE (show NAPA Proteins) is SNAP-25; v-SNARE (show VTI1B Proteins) is VAMP2 (show VAMP2 Proteins).)
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 (show FOXC1 Proteins)-C.
Robust association of the rs3746544 SNP and ASD (show ARSD Proteins), 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.
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 (show NAPA Proteins) assembly pathway underlying regulated exocytosis.
microdomains carrying syntaxin1 (show STX1A Proteins)/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 (show NAPA Proteins) proteins VAMP-2 (show VAMP2 Proteins) 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