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involved in myocardial fatty acid uptake. Additionally we are shipping and and many more products for this protein.
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Several proteins that are expressed in the epidermis have been proposed to facilitate the uptake of long-chain fatty acids (LCFA) in mammalian cells, CD36 (show CD36 ELISA Kits), fatty acid binding protein (show FABP ELISA Kits), and FATP. [review]
FATP1 inhibits 11-cis (show CISH ELISA Kits) retinol formation via interaction with the visual cycle retinoid isomerase RPE65 (show RPE65 ELISA Kits) and lecithin:retinol acyltransferase
exogenously supplied fatty acids are preferentially channeled by an FATP1-linked mechanism into the TG biosynthetic pathway; such internalized lipids downregulate de novo sphingomyelin and cholesterol metabolism in growing 293 cells
FATP1 might play a role in post-prandial lipid metabolism and development of cardiovascular disease.
FATP1 stimulated transport and consumption of palmitate and oleate, which they channeled away from complete oxidation and toward TAG synthesis.
These data reveals the localization and points to a regulatory function of FATP1 in myotube mitochondria.
Transgenic expression of FATP1 in suprabasal keratinocytes rescued the phenotype of Fatp4 (show SLC27A4 ELISA Kits) mutants, and FATP1 sorted to the same intracellular organelles as endogenous FATP4 (show SLC27A4 ELISA Kits)
FATP1 was localized in mitochondria, in the outer membrane and intermembrane parts, of mouse skeletal muscle
Fatp1 deficiency affects retinal light response and dark adaptation, and induces age-related alterations.
microRNA-mediated silencing of TR4 (show NR2C2 ELISA Kits) in 3T3-L1 adipocytes drastically reduced basal FATP1 5' promoter activity and FATP1 expression with reduced lipid accumulation.
Overexpression of Fatp1 in skeletal muscle increased the rate of long-chain fatty acid transport and channelled these lipids to oxidation, not to intramuscular lipid accumulation.
The FATP1 enhanced the activity of 2-oxoglutarate dehydrogenase independently of its acyl-CoA synthetase activity whereas silencing of FATP1 in 3T3-L1 adipocytes resulted in decreased activity of 2-oxoglutarate dehydrogenase.
FATP1, like FAT/CD36 (show CD36 ELISA Kits), is associated with mitochondria and has a role in mitochondrial oxidation of fatty acids.
Insulin (show INS ELISA Kits) causes fatty acid transport protein (show CD36 ELISA Kits) translocation
FATP1 homodimeric complexes play an important role in cellular fatty acid import.
These results indicate the associations of g.28470 T>C and g.28672 G>A with meat quality traits in Qinchuan cattle. Thus, the FATP1 gene may be used in marker-assisted selection of beef cattle in breeding programs.
Cattle SNPs in exon 3 and the 3'-flanking region of the SLC27A1 gene showed that cows with genotype CC had higher milk yields than those with genotype TC (0.01 < p < 0.05).
The bovine SLC27A1 gene is organized in 13 exons. It extends over more than 40 kb of genomic DNA. Complex regulation mechanisms may be involved in determining the final SLC27A1 protein levels in each tissue.
Fourteen new single nucleotide polymorphisms were identified in SLC27A1; no significant differences in milk fat content of Holstein-Friesians were associated with the polymorphisms and in 2 Spanish breeds all positions except 2 were polymorphic.
involved in myocardial fatty acid uptake
, fatty acid transport protein 1
, long-chain fatty acid transport protein 1
, solute carrier family 27 member 1
, solute carrier family 27, member 1
, fatty acid transport protein-1
, fatty acid transporter 1c