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The protein encoded by STRA6 is a membrane protein involved in the metabolism of retinol. Additionally we are shipping STRA6 Antibodies (77) and STRA6 Proteins (6) and many more products for this protein.
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A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.
These data establish that holo-RBP (show RBP4 ELISA Kits) and its receptor STRA6 are potent oncogenes and suggest that the pathway is a novel target for therapy of some human cancers.
Evidence for the existence of a transmembrane pore, analogous to the pore of ion channels, in STRA6.
STRA6 has a role for regulating retinoid homeostasis and in helping to program signaling that drives proliferation and differentiation of human skin cells
Stra6, a retinoic acid-responsive (show GPRC5A ELISA Kits) gene, participates in p53 (show TP53 ELISA Kits)-induced apoptosis after DNA damage.
Analysis of FRAS1 (show FRAS1 ELISA Kits) and STRA6 mutations in the same family with eye anomalies.
Findings suggest that heterozygosity for the STRA6 gene mutation may be associated with ocular abnormalities.
TTR (show TTR ELISA Kits) blocks the ability of holo-retinol-binding protein to associate with STRA6 and thereby effectively suppresses both STRA6-mediated retinol uptake and STRA6-initiated cell signaling.
STRA6 orchestrates a multicomponent machinery that couples vitamin A homeostasis and metabolism to activation of a signaling cascade and that, in turn, STRA6 signaling regulates the cellular uptake of the vitamin.
STRA6 mutations can cause isolated eye malformations in addition to the congenital anomalies observed in MWS.
Studies indicate that STRA6 is indeed a bona fide vitamin A transporter and provide novel insights into the regulatory mechanism that governs vitamin A homeostasis in peripheral tissues.
Total vitamin A levels are dramatically lower in the eyes of STRA6 KO mice as compared to those of WT mice, but the levels in other organs were not significantly affected after STRA6 deletion under vitamin A sufficient conditions.
STRA6 reduction in adipocytes in adipose-Stra6(-/-) mice.
Rbp4 (show RBP4 ELISA Kits) and its membrane receptor STRA6 control adipogenesis by regulating cellular retinoid homeostasis and RARalpha (show RARA ELISA Kits) activity.
STRA6 in tissues other than the eye appears to be the coupling of circulating holo-RBP (show RBP4 ELISA Kits) levels to cell signaling, in turn regulating key processes such as insulin (show INS ELISA Kits) response.
Stra6, a retinoic acid-responsive gene, participates in p53 (show TP53 ELISA Kits)-induced apoptosis after DNA damage.
LRAT (show LRAT ELISA Kits) acts together with Cyp26A1 (show CYP26A1 ELISA Kits), one of the enzymes that catalyze the degradation of retinoic acid, and possibly with STRA6, the recently identified cell surface receptor for retinol-RBP (show RBP4 ELISA Kits)
STRA6 was identified in retinal pigment epithelium cells as a specific membrane receptor for retinol binding protein (RBP (show RBP4 ELISA Kits)); STRA6 binds to RBP (show RBP4 ELISA Kits) with high affinity and has robust vitamin A uptake activity from the vitamin A-RBP (show RBP4 ELISA Kits) complex
study identifies an essential functional domain in STRA6
The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene.
stimulated by retinoic acid gene 6 homolog
, stimulated by retinoic acid gene 6 protein homolog
, stimulated by retinoic acid 6 homolog
, retinoic acid-responsive protein
, stimulated by retinoic acid gene 6 protein