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The intracellular fatty acid-binding proteins (FABPs) belong to a multigene family with nearly twenty identified members.
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Rat (Rattus) FABP2 ELISA Kit für Sandwich ELISA - ABIN431574
Chi, Yao, Xia, Jin, Li, Cai, Hei: Elevation of HO-1 Expression Mitigates Intestinal Ischemia-Reperfusion Injury and Restores Tight Junction Function in a Rat Liver Transplantation Model. in Oxidative medicine and cellular longevity 2015
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Human FABP2 ELISA Kit für Sandwich ELISA - ABIN365736
Zhang, Fan, Zhong, Xu, Shen: Association of plasma diamine oxidase and intestinal fatty acid-binding protein with severity of disease in patient with heat stroke. in The American journal of emergency medicine 2015
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Mouse (Murine) FABP2 ELISA Kit für Sandwich ELISA - ABIN424242
Kowalska, Olejnik, Rychlik, Grajek: Cranberries (Oxycoccus quadripetalus) inhibit lipid metabolism and modulate leptin and adiponectin secretion in 3T3-L1 adipocytes. in Food chemistry 2015
Rat (Rattus) FABP2 ELISA Kit für Sandwich ELISA - ABIN366484
Lu, Kang, Zhan, Lv, Fan, Wang, Ali, Lv, Li, Mu: Dai Huang Fu Zi Tang could ameliorate intestinal injury in a rat model of hemorrhagic shock by regulating intestinal blood flow and intestinal expression of p-VASP and ZO-1. in BMC complementary and alternative medicine 2014
In vivo experiments demonstrated, for the first time, that intestinal absorption of dietary BODIPY-FLC(12) was followed by colocalization of the labeled FA with Fabp1b and Fabp2 in the nuclei.
transcription of single copy fabp2 is modulated by dietary fatty acids and clofibrate in a tissue specific fashion.
Ifabp mRNAs were initially expressed in the zebrafish yolk syncytial layer at the ventral side during late epiboly (8-9 hpf), spread throughout the YSL of later stage embryos, and appeared in the intestine rudiment at approximately 36 hpf
analysis of conserved elements that mediate intestinal-type fatty acid binding protein (I-FABP) expression in the gut (zeige GUSB ELISA Kits) epithelia of zebrafish larvae
dna analysis, linkage mapping and early developmental expression of the intestinal-type fatty acid-binding protein gene (fabp2) from zebrafish
Data show that intestinal fatty acid binding protein (IFABP) is a promising prognostic marker in acute pancreatitis.
There was a positive correlation between FABP2 levels and BMI, SBP (zeige SHBG ELISA Kits) and DBP (zeige GC ELISA Kits), and a negative correlation with HDL (zeige HSD11B1 ELISA Kits)-C. CONCLUSIONS: The Thr54 allele of the FABP2 Ala54Thr polymorphism was associated with an increased incidence of peripheral atherosclerosis combined with T2DM in the population studied
The FABP-2 gene is located on the long arm of chromosome 4, and encodes an intracellular protein of the intestinal mucosa, responsible for the absorption and intracellular transport of fatty acids.
Enterocyte injury was common in critically ill patients with pneumonia. The severity of enterocyte injury, as evidenced by the urinary FABP2/creatinine, was associated with the patient's mortality.
Study reports that insulin (zeige INS ELISA Kits) resistance-related gene polymorphisms effects colorectal cancer (CRC (zeige CALR ELISA Kits)) risk. The results showed that the gene polymorphism of ADIPOQ rs2241766 was associated with CRC (zeige CALR ELISA Kits) risk. Furthermore, the interactions of ADIPOQ rs2241766, UCP2 (zeige UCP2 ELISA Kits) rs659366, FABP2 rs1799883 and red meat consumption may contribute to the risk of CRC (zeige CALR ELISA Kits).
FTO (zeige FTO ELISA Kits) and FABP2 gene polymorphisms were significantly associated with susceptibility to metabolic syndrome and obesity in this cohort.
Circulating I-FABP levels had no association with invasively-measured hemodynamic parameters, but were associated with adverse clinical outcomes in patients with acute decompensated heart failure with systolic dysfunction.
The aim of this study was to measure serum I-FABP levels and provide the transition of I-FABP levels with hypothermic circulatory arrest to help in the management of intestinal perfusion. Plasma I-FABP monitoring could be a valuable method for finding an intestinal ischemia in patients with cardiovascular surgery.
Urinary intestinal fatty acid-binding protein can distinguish necrotizing enterocolitis from sepsis in early stage of the disease.
I-FABP is a valid serologic biomarker for early diagnosis in NEC for the premature neonates with a moderate accuracy.
The full-length cDNA of I-FABP was cloned from intestine and the mRNA was extensively present in various tissues, but I-FABP transcript of approximately 620 bp was more abundant in intestine than in other tissues.
Plasma I-FABP concentration showed great variation within treatments, and no difference was observed in plasma I-FABP concentrations between the weaned conventionally and unweaned treatments
Association analyses of the FABP2:g.412T>C with fatty acid composition traits were not significant in simple association.
This direct comparison provides evidence that LFABP (zeige FABP1 ELISA Kits) and IFABP have distinct roles in intestinal lipid metabolism; differential intracellular functions in intestine and in liver
detected the common as well as sex-differential pathways that are modified due to the loss of Fabp2. These findings suggest that the pathways involved in nutrient and xenobiotic metabolism in the intestine are regulated by sex-specific mechanisms
loss of I-FABP renders male mice sensitive to high fat diet-induced fatty liver, and this effect is independent of hepatic L-FABP
The intracellular fatty acid-binding proteins (FABPs) belong to a multigene family with nearly twenty identified members. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Intestinal fatty acid-binding protein 2 gene contains four exons and is an abundant cytosolic protein in small intestine epithelial cells. This gene has a polymorphism at codon 54 that identified an alanine-encoding allele and a threonine-encoding allele. Thr-54 protein is associated with increased fat oxidation and insulin resistance.
, fatty acid-binding protein, intestinal
, intestinal fatty acid binding pr
, intestinal fatty acid binding protein 2
, fatty acid binding protein 2, intestinal
, fatty acid-binding protein 2
, intestinal-type fatty acid-binding protein
, fatty acid binding protein 1
, intestinal fatty acid binding protein
, intestinal fatty acid-binding protein
, fatty acid binding protein 2, intestinal a
, fatty acid-binding protein, intestinal a