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The intracellular fatty acid-binding proteins (FABPs) belong to a multigene family with nearly twenty identified members. Additionally we are shipping FABP2 Kits (59) and FABP2 Proteins (42) and many more products for this protein.
Showing 10 out of 172 products:
Human Monoclonal FABP2 Primary Antibody for ICC, FACS - ABIN969124
Yamada, Yuan, Ishiyama, Koyama, Ichikawa, Koyanagi, Koyama, Nonaka: Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men. in Diabetologia 1997
Show all 4 references for ABIN969124
Human Polyclonal FABP2 Primary Antibody for IHC (p), IHC - ABIN252953
Venold, Penn, Thorsen, Gu, Kortner, Krogdahl, Bakke: Intestinal fatty acid binding protein (fabp2) in Atlantic salmon (Salmo salar): Localization and alteration of expression during development of diet induced enteritis. in Comparative biochemistry and physiology. Part A, Molecular & integrative physiology 2012
Show all 4 references for ABIN252953
Cow (Bovine) Polyclonal FABP2 Primary Antibody for EIA, IHC (p) - ABIN374817
Takakura, Yoshioka, Umekawa, Kogure, Toda, Yoshikawa, Yoshida: Thr54 allele of the FABP2 gene affects resting metabolic rate and visceral obesity. in Diabetes research and clinical practice 2004
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 (show GUSB Antibodies) epithelia of zebrafish larvae
dna analysis, linkage mapping and early developmental expression of the intestinal-type fatty acid-binding protein gene (fabp2) from zebrafish
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.
It is concluded that ACE (show ACE Antibodies) (rs 4646994), FABP2 (rs1799883) and GST (show SLCO6A1 Antibodies) (GSTM1 (show GSTM1 Antibodies) null or positive genotype and GSTT1 (show GSTT1 Antibodies) null or positive genotype) genes polymorphism are associated with essential hypertension.
Ala54Thr polymorphism of FABP2 modulates HDL (show HSD11B1 Antibodies) cholesterol in Mexican-Americans with type 2 diabetes.
Carriers of the Thr54 allele in FABP2 have a different metabolic response after weight loss than wild type non-A obese carriers
Letter: serum intestinal-fatty acid binding protein may serve as a biomarker for refractory celiac disease.
Ala54Thr polymorphism of FABP2 was associated with high triglycerides levels, but not to gallstone disease.
FABP2 Ala54Thr polymorphism may have a role in type 2 diabetes, obesity, and metabolic syndrome [case-control study and meta-analysis]
Both plasma and urinary I-FABP levels specifically identify necrotizing enterocolitis in preterm infants.
FABP2 is a gene candidate for predisposition to Diabetic nephropathy, as it has been linked to microalbuminuria in patients with Type 2 Diabetes mellitus.
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 (show FABP1 Antibodies) 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