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The gene is a member of the syntaxin family. Additionally we are shipping STX3 Proteins (9) and many more products for this protein.
Showing 10 out of 22 products:
Human Polyclonal STX3 Primary Antibody for EIA, IHC (p) - ABIN357986
Darios, Davletov: Omega-3 and omega-6 fatty acids stimulate cell membrane expansion by acting on syntaxin 3. in Nature 2006
Show all 3 references for ABIN357986
Human Polyclonal STX3 Primary Antibody for EIA, IHC (fro) - ABIN1109188
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. in Molecular biology of the cell 1998
we report for the first time a missense mutation of a novel lens specific gene STX3 in a phenotype associating autosomal recessive congenital cataract and intellectual disability.
GLUT5 (show SLC2A5 Antibodies) required an interaction cascade of Rab11 (show RAB11A Antibodies), Myo5B, Slp4a, Munc18-2 (show STXBP2 Antibodies), and Vamp7 (show VAMP7 Antibodies) with Stx3.
Rab11a (show RAB11A Antibodies)-knockdown cells displayed mislocalization of STX3 and the presentation of microvilli in the basolateral compartment
the secretion of IL-1alpha, IL-1beta (show IL1B Antibodies), IL-12b (show IL12B Antibodies), and CCL4 (show CCL4 Antibodies) occurs during gelatinase degranulation, a process controlled by STX3.
The results showed that there was reduction in aggregation propensity of syntaxin-3 with point mutation at Val286.
hcmv-miR (show MLXIP Antibodies)-US33-5p-mediated inhibition of HCMV DNA synthesis and of viral replication are specifically mediated by down-regulation of STX3 expression.
loss of STX3 function causes variant microvillus inclusion disease
In insulin (show INS Antibodies) secretion, SYN-3 (show SYN3 Antibodies) plays a role in the mediation of newcomer SG exocytosis and SG-SG fusion that contributes to biphasic GSIS.
STX-3 and SNAP-23 (show SNAP23 Antibodies) are crucial for the release of all chemokines in mature human mast cells
These results demonstrate a function for STX3 in human cytomegalovirus morphogenesis, and unravel a new role for this SNARE (show NAPA Antibodies) protein in late endosomes/lysosomes compartments.
Phosphorylation of syntaxin 3B by CaMKII (show CAMK2G Antibodies) can modulate the assembly of the SNARE (show VTI1B Antibodies) complex in ribbon synapses of the retina.
The SNARE (show VTI1B Antibodies) machinery composed of VAMP7 (show VAMP7 Antibodies) on Tyrp1 (show TYRP1 Antibodies)-containing vesicles and syntaxin-3 and SNAP23 (show SNAP23 Antibodies) on melanosomes regulates Tyrp1 (show TYRP1 Antibodies) trafficking to the melanosome in melanocytes.
In insulin (show INS Antibodies) secretion, SYN-3 plays a role in the mediation of newcomer SG exocytosis and SG-SG fusion that contributes to biphasic GSIS.
Results show that cells in the mouse retina express only syntaxin 3B, while nonneuronal tissues, such as kidney, express only syntaxin 3A.
The gene is a member of the syntaxin family. The encoded protein is targeted to the apical membrane of epithelial cells where it forms clusters and is important in establishing and maintaining polarity necessary for protein trafficking involving vesicle fusion and exocytosis. Alternative splicing results in multiple transcript variants.
, syntaxin 3
, syntaxin 3A
, syntaxin 3B