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OSBPL1A encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Additionally we are shipping Oxysterol Binding Protein-Like 1A Proteins (5) and many more products for this protein.
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Human Polyclonal OSBPL1A Primary Antibody for ELISA, WB - ABIN185115
Lehto, Laitinen, Chinetti, Johansson, Ehnholm, Staels, Ikonen, Olkkonen: The OSBP-related protein family in humans. in Journal of lipid research 2001
Show all 2 references for ABIN185115
Human Polyclonal OSBPL1A Primary Antibody for EIA, WB - ABIN953942
Hanna, Kruskal, Ezekowitz, Bloom, Collier: Role of macrophage oxidative burst in the action of anthrax lethal toxin. in Molecular medicine (Cambridge, Mass.) 1996
Show all 2 references for ABIN953942
The L66P mutation in the first doublecortin (show DCX Antibodies) domain of the Rp1 (show STK19 Antibodies) gene impairs Rp1 (show STK19 Antibodies) protein localization and function, leading to abnormalities in photoreceptor outer segment structure and progressive photoreceptor degeneration.
We suggest that arRP patients with high myopic refractive error should be preferentially analysed for RP1 (show STK19 Antibodies) mutations.
it reports that different regions of RP1 (show STK19 Antibodies) can also lead to arRCD.
Two novel heterozygous null mutations in RP1 (show STK19 Antibodies) co-segregate with the disease in autosomal recessive retinitis pigmentosa patients.
RP1 (show STK19 Antibodies) phosphorylation at Ser (show SIGLEC1 Antibodies)(236) by CK2 (show CSNK2A1 Antibodies) seems to play a significant role in cell adhesion and might initiate new insights in the CK2 (show CSNK2A1 Antibodies) and EB1 (show MAPRE2 Antibodies) family protein association.
Data found pathogenic DNA variants in the genes RP1 (show STK19 Antibodies), USH2A (show USH2A Antibodies), CNGB3 (show CNGB3 Antibodies), NMNAT1 (show NMNAT1 Antibodies), CHM (show CHM Antibodies), and ABCA4 (show ABCA4 Antibodies), responsible for retinitis pigmentosa, Usher syndrome, achromatopsia, Leber congenital amaurosis, choroideremia (show CHM Antibodies), or recessive Stargardt/cone-rod dystrophy cases.
The most severe missense mutation occurred in patients with p.D984G in RP1 (show STK19 Antibodies).
A novel homozygous retinitis pigmentosa nonsense mutation in exon 4 of the RP1 (show STK19 Antibodies) gene, c.1012C>T (p.R338*) was identified in the proband and her two affected sisters.
molecular mechanism of RP1 (show STK19 Antibodies) mutation
ORP1S is a cytoplasmic sterol sensor, which transports sterols to the nucleus and promotes LXR (show NR1H3 Antibodies) regulated trans-activation of apoE (show APOE Antibodies).
Osbpl1a silencing in macrophage foam cells enhances endosome motility and results in inhibition of [(3)H]cholesterol efflux to apolipoprotein A-I (show APOA1 Antibodies).
OSBP (show OSBP Antibodies) regulates hepatic TG metabolism and suggest the involvement of OSBP (show OSBP Antibodies) in the insulin (show INS Antibodies) signaling pathways that control hepatic lipogenesis.
This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although some members contain only the sterol-binding domain. Transcript variants derived from alternative promoter usage and/or alternative splicing exist\; they encode different isoforms.
oxysterol-binding protein-related protein 1
, oxysterol-binding protein-like 1A
, oxysterol binding protein-like 1A
, oxysterol binding protein-like protein 1A
, oxysterol-binding protein-related protein 1-like
, OSBP-related protein 1
, oxysterol binding protein-like 1B
, oxysterol-binding protein-related protein 1 variant 1
, oxysterol-binding protein-related protein 1 variant 2
, oxygen-regulated protein 1
, retinitis pigmentosa 1 protein
, retinitis pigmentosa RP1 protein