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SELS encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. Additionally we are shipping Selenoprotein S Kits (6) and Selenoprotein S Proteins (3) and many more products for this protein.
Showing 10 out of 42 products:
Cow (Bovine) Polyclonal SELS Primary Antibody for WB - ABIN2783218
Moses, Johnson, Tømmerdal, Forsmo, Curran, Abraham, Charlesworth, Brennecke, Blangero, Austgulen: Genetic association of preeclampsia to the inflammatory response gene SEPS1. in American journal of obstetrics and gynecology 2008
Show all 3 references for ABIN2783218
Human Polyclonal SELS Primary Antibody for ICC, IF - ABIN4352486
Bubenik, Miniard, Driscoll: Alternative transcripts and 3'UTR elements govern the incorporation of selenocysteine into selenoprotein S. in PLoS ONE 2013
Show all 3 references for ABIN4352486
Human Polyclonal SELS Primary Antibody for IP, WB - ABIN527713
Huang, Hsiao, Chu, Ye, Chen: Derlin2 protein facilitates HRD1-mediated retro-translocation of sonic hedgehog at the endoplasmic reticulum. in The Journal of biological chemistry 2013
interaction between SelK (show HSP Antibodies) and p97(VCP (show vcp Antibodies)) is SelS-dependent, and the resulting ERAD complex (SelS-p97(VCP (show vcp Antibodies))-SelK (show HSP Antibodies)) plays an important role in ERAD and ER stress
Potential roles of the SEPS1 gene in the pathogenesis and etiology of Hashimoto's thyroiditis.
SNP rs4965814 of SELS may affect the susceptibility to ischemic stroke.
The SEPS1 -105G>A is associated with an increased risk of Kashin-Beck disease and influences the expression of PI3K (show PIK3CA Antibodies)/Akt (show AKT1 Antibodies) signaling pathway in Kashin-Beck disease patients
Although VIMP can interact with CLIMP-63 (show CKAP4 Antibodies) and Syn5L, it does not interact with MT-binding ER proteins (such as Reep1 (show REEP1 Antibodies)) that shape the tubular smooth ER
Selenoprotein S is a marker but not a regulator of endoplasmic reticulum stress in intestinal epithelial cells in inflammatory bowel diseases.
Pro(178) and Pro(183) of SelS play important roles in the translocation of p97(VCP (show vcp Antibodies)) to the ER membrane and protect cells from ER stress
that SEPS1 may protect mice against LPS (show IRF6 Antibodies)-induced sepsis and organ damage. Therefore, SEPS1 may be a new target to resolve LPS (show IRF6 Antibodies)-induced sepsis.
Existence of a link between SEPS1 promoter genetic variation and Hashimoto thyroiditis risk.
Findings suggest that the SEPS1 G-105A polymorphism contributes to the risk of developing SPTB (show SPTB Antibodies) in a Chinese population.
SelS expression is prominent in neurons and hardly detectable in astrocytes from control mice
The SEPS1 protein expression in liver of septic mouse is markedly elevated.
These findings suggest that SEPS1 could be a new ER stress-dependent survival factor that protects macrophage against ER stress-induced cellular dysfunction.
We found that suppression of SEPS1 by small interfering RNA severely increases astrocyte injure caused by OGD (show FGFR1 Antibodies), suggesting that selenoprotein S protects astrocytes against ischemia.
This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Studies suggest that this protein may regulate cytokine production, and thus play a key role in the control of the inflammatory response. Two alternatively spliced transcript variants encoding the same protein have been found for this gene.
, histocompatibility 47
, minor histocompatibility antigen H47