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FABP6 encodes the ileal fatty acid binding protein. Zusätzlich bieten wir Ihnen FABP6 Antikörper (63) und FABP6 Proteine (28) und viele weitere Produktgruppen zu diesem Protein an.
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Structural determinants of ligand binding in the ternary complex of human ileal bile acid binding protein with glycocholate and glycochenodeoxycholate obtained from solution NMR
Analysis of slow and fast motions in I-BABP indicates largely different energy landscapes for the apo (zeige C9orf3 ELISA Kits) and holo states suggesting that optimization of binding interactions might be achieved by altering the dynamic behavior of specific protein segments.
show, using electrospray ionization mass spectroscopy, that human ILBP binds bile acids with a 3:1 ratio, even at low protein and ligand concentrations
Ursodeoxycholic acid induces unique conformational changes in IBABP.
NMR data are in agreement with a conformational selection model we proposed earlier for I-BABP and support the hypothesis of an allosteric mechanism of ligand binding
The-putative functional-Thr79Met substitution of FABP6 confers a protective effect on type 2 diabetes in obese individuals.
NMR structure of human ileal lipid-binding protein-cholyltaurine complex and its comparison with homologous structures
the I-BABP gene may be a novel target for PPAR (zeige PPARA ELISA Kits) in humans
ASBT and ILBP protein were 48% and 67% lower in normal weight gallstone carriers than in controls (P < 0.05); similar differences were found for mRNA expression levels.
The expression of FABP6 was higher in primary colorectal cancers and adenomas than in normal epithelium, but was dramatically decreased in lymph node metastases, suggesting that FABP6 may play an important role in early carcinogenesis.
expression of the Fabp6 gene in granulosa cells serves an important and previously unrecognized function in fertility
The results demonstrate that ilbp is involved in the apical to basolateral transport of bile acids in ileal enterocytes, and is vital for the maintenance of bile acid homeostasis in the enterohepatic circulation (EHC) in mice.
The ligand binding activity of purified recombinant murine ILBP (mILBP) in vitro; mILBP exhibits a preference for certain species of bile and fatty acids.
The lithogenic diet induced biliary hyperplasia and reduced bile salt transporter FABP6 expression in C57L mice.
This gene encodes the ileal fatty acid binding protein. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABP6 and FABP1 (the liver fatty acid binding protein) are also able to bind bile acids. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism. Transcript variants generated by alternate transcription promoters and/or alternate splicing have been found for this gene.
fatty acid binding protein 6, ileal (gastrotropin)
, fatty acid binding protein 6, ileal
, ileal bile acid binding protein
, ileal lipid-binding protein
, illeal lipid-binding protein
, intestinal 15 kDa protein
, 14 kDa bile acid-binding protein
, Fatty acid binding protein 6 (bile acid-binding protein)
, fatty acid-binding protein 6
, strain SHR/OlaIpcv fatty acid binding protein 6 (Fabp6) pseudogene
, porcine ileal peptide
, ileal bile acid-binding protein