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NIPSNAP1 encodes a member of the NipSnap family of proteins that may be involved in vesicular transport. Zusätzlich bieten wir Ihnen 4-Nitrophenylphosphatase Domain and Non-Neuronal SNAP25-Like Protein Homolog 1 (C. Elegans) Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal NIPSNAP1 Primary Antibody für IHC (p), WB - ABIN541700
Seroussi, Pan, Kedra, Roe, Dumanski: Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family. in Gene 1998
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Human Polyclonal NIPSNAP1 Primary Antibody für IHC (p), WB - ABIN541701
Surendran, Tyring, Matalon: Expression of calpastatin, minopontin, NIPSNAP1, rabaptin-5 and neuronatin in the phenylketonuria (PKU) mouse brain: possible role on cognitive defect seen in PKU. in Neurochemistry international 2005
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NIPSNAP1 is an interacting molecule of NST and plays a crucial role in pain transmission.
This study presents the first physiological function of Nipsnap1 as an associated protein inhibiting transient receptor potential vanilloid channel 6 activity that possibly exerts its effect directly at the plasma membrane.
Data suggest that amyloid precursor proteins may affect mitochondrial function through a direct interaction with NIPSNAP1 as well as with other mitochondrial proteins.
identified mitochondrial proteins 4-nitrophenylphosphatase domain and non-neuronal synaptosomal associated protein 25-like protein homolog (NIP-SNAP)-1 and -2 as clarithromycin-binding proteins. Production of proinflammatory cytokines induced by lipopolysaccharides and Pam3-CSK4 in epithelial cell lines BEAS-2B and T24 were suppressed by knockdown of NIP-SNAP-1 or -2
NIP-SNAP-1 and -2 localized in the mitochondrial inner membrane space, whereas HSP60 localized in the matrix. Expression levels of NIP-SNAP-1 and -2 in cells were decreased by knockdown of HSP60, but not HSP10. The findings indicate that HSP60 promotes folding and maintains the stability of NIP-SNAP-1 and -2.
These results suggest that changes in NIPSNAP1 expression may contribute to the pathogenesis of inflammatory pain.
Structural variants unique to the malignant cell line inactivated: gene NIPSNAP1, putative tumor suppressor that inhibits TRPV6, an anti-apoptotic oncogene implicated in prostate cancer progression.
NIPSNAP1 mutations could not explain phenotype of patients with combined oxidative phosphorylation system deficiencies.
This study presents the first physiological function of mouse Nipsnap1 as an associated protein inhibiting transient receptor potential vanilloid channel 6 activity that possibly exerts its effect directly at the plasma membrane.
This gene encodes a member of the NipSnap family of proteins that may be involved in vesicular transport. A similar protein in mice inhibits the calcium channel TRPV6, and is also localized to the inner mitochondrial membrane where it may play a role in mitochondrial DNA maintenance. A pseudogene of this gene is located on the short arm of chromosome 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
4-nitrophenylphosphatase domain and non-neuronal SNAP25-like protein homolog 1
, protein NipSnap homolog 1
, 4-nitrophenylphosphatase domain and non-neuronal SNAP25-like 1