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Mouse (Murine) FABP4 ELISA Kit for Sandwich ELISA - ABIN2684218
Uysal, Scheja, Wiesbrock, Bonner-Weir, Hotamisligil: Improved glucose and lipid metabolism in genetically obese mice lacking aP2. in Endocrinology 2000
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Human FABP4 ELISA Kit for Sandwich ELISA - ABIN2684217
Fu, Luo, Lopes-Virella: Oxidized LDL induces the expression of ALBP/aP2 mRNA and protein in human THP-1 macrophages. in Journal of lipid research 2001
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Human FABP4 ELISA Kit for Sandwich ELISA - ABIN414793
Yoon, Sung, Song, Lee, Rhee, Shin, Yoo, Chae, Kim, Jin, Cho: Enhanced A-FABP expression in visceral fat: potential contributor to the progression of NASH. in Clinical and molecular hepatology 2012
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Rat (Rattus) FABP4 ELISA Kit for Sandwich ELISA - ABIN457201
Martinez-Arguelles, Campioli, Lienhart, Fan, Culty, Zirkin, Papadopoulos: In utero exposure to the endocrine disruptor di-(2-ethylhexyl) phthalate induces long-term changes in gene expression in the adult male adrenal gland. in Endocrinology 2014
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Human FABP4 ELISA Kit for Sandwich ELISA - ABIN579439
Ciborowski, Zbucka-Kretowska, Bomba-Opon, Wielgos, Brawura-Biskupski-Samaha, Pierzynski, Szmitkowski, Wolczynski, Lipinska, Citko, Bauer, Gorska, Kretowski: Potential first trimester metabolomic biomarkers of abnormal birth weight in healthy pregnancies. in Prenatal diagnosis 2014
serum A-FABP levels were increased significantly in normoglycemic individuals with a first-degree family history of diabetes; the use of serum A-FABP as a biomarker in the first-degree relatives of patients with diabetes may result in overestimation of the risk of obesity-induced metabolic disease and cardiovascular disease
Findings in the dorsolateral prefrontal cortex in schizophrenia provide evidence of altered proteins involved in synaptic function (FABP4), cytoarchitecture organization (NEFH (show NEFH ELISA Kits)), and circadian molecular clock signaling (CSNK1E (show CSNK1E ELISA Kits)), which may be contributing to the cognitive and/or negative symptoms in this disorder. FABP4, CSNK1E (show CSNK1E ELISA Kits) and NEFH (show NEFH ELISA Kits) could become potentially useful biomarkers for schizophrenia.
Circulating levels of AFABP and EFABP are not decreased in Lipodystrophy despite adipose tissue loss in contrast to other adipokines including leptin and adiponectin.
Taken together, PPAR gamma (show PPARG ELISA Kits) and FABP4 gene expression levels in PBMCs [peripheral blood mononuclear cells] may be indicators of metabolic factors and body composition components.
eFABP4 induces ER stress and potentiates the effect of linoleic acid in HepG2 cells, suggesting that FABP4 could be a link between obesity-associated metabolic abnormalities and hepatic insulin (show INS ELISA Kits) resistance mechanisms
Increased second-trimester FABP4 independently predicted pre-eclampsia in women with type 1 diabete and significantly improved reclassification and discrimination.
High levels of FABP4 are significantly related to stroke risk and severity, independent from other traditional and emerging risk factors, suggesting that they may play a role in stroke pathogenesis.
We found that serum FABP4 concentration were associated with insulin (show INS ELISA Kits) resistance and secretion in type 2 diabetes mellitus. This suggests that FABP4 may play an important role in glucose homeostasis.
High FABP4 expression is associated with ovarian cancer.
AFABP levels were higher in neonates compared with adults. Preterm infants had higher AFABP levels compared with full-term infants. Among full-term infants, AFABP levels in SGA infants were lower, compared with appropriate for gestational age and large for gestational age infants.
Overexpressed FABP4 of different genotypes in bovine intramuscular preadipocytes and studied the intracellular localization of FABP4 and the expression levels of lipid metabolism-related genes among different genotypes.
These results provide an important basis for further understanding the regulation of bovine FABP4.
This suggest that FABP4 affects milk yield and milk protein (show CSN2 ELISA Kits) content, both economically important traits, and that further study of this gene is warranted.
Data show that overexpression of cattle adipocyte fatty acid-binding protein (A-FABP)gene promoted fat deposition in the skeletal muscle of transgenic mice.
FABP4 gene frequency and SNP genotypes in Holstein-Friesian cows and its relationship with protein and fat content in milk
The effects of genetic polymorphisms of liver X receptor, alpha (LXR (show NR1H3 ELISA Kits)), stearoyl-CoA desaturase (SCD (show SCD ELISA Kits)), Fatty acid synthase (FASN (show FASN ELISA Kits)), and Fatty acid binding protein 4 (FABP4) were investigated on fatty acid composition in fat tissue of steers.
re-sequenced 4.3 kb of the FABP4 gene region in 24 Hanwoo bulls and identified 16 SNPs and 1 microsatellite polymorphism.
The FABP4 gene falls into a suggestive/significant quantitative trait loci interval for beef marbling.
Our findings suggest that the polymorphisms in FABP4 may play a role in determining one of the important genetic factors that influence back fat thickness in beef cattle.
FABP4 I74V polymorphism had a significant effect on palmitoleic acid composition in intramuscular fat.
FABP4 gene expression level in adipose tissue was higher than in muscle. In contrast, FABP5 was expressed at low levels in adipocytes and muscle tissues. Low and moderate correlations between FABP4 and FABP5 gene expression were observed in muscle and in backfat, respectively.
the A-FABP gene is strongly related to the development and function of intramuscular fat accretion in pigs.
AFABP is significantly increased in coronary artery in-stent restenosis segments of both diabetic and nondiabetic minipigs.
Thus A-FABP may be a candidate gene or a quantitative trait locus-linked gene associated with meat quality traits.
Monitoring of posttransplant L-FABP plasma levels is a valuable new tool to quantify early the extent of parenchymal cell damage of non-heart-beating donors in liver transplantation.
study suggests that FABP-4 protein content may be a valuable marker of lipid accretion
A study of the mapping characteristics and relationship to body composition of FAT1 and FABP4 in swine is reported.
regenerated coronary endothelial cells exhibit upregulation of adipocyte fatty acid binding protein (A-FABP)
describe the regulation at the duplicated zebrafish fabp7a/fabp7b, fabp10a/fabp10b and fabp11a/fabp11b gene promoters.
Upregulated ROS (show ROS1 ELISA Kits) induced by FABP4 was of significance in activating FoxM1 (show FOXM1 ELISA Kits) leading to airway inflammation and epithelial barrier dysfunction.
Collectively, these results demonstrate that C. pneumoniae exploits host FABP4 to facilitate fat mobilization and intracellular replication in adipocytes. This work uncovers a novel strategy used by intracellular pathogens for acquiring energy via hijacking of the host lipid metabolism pathway.
High Fabp4 expression is associated with Acute myeloid leukemia (show BCL11A ELISA Kits).
These data suggest that the function of SIRT6 (show SIRT6 ELISA Kits) in the Fabp4-Cre-expressing cells in addition to mature adipocytes plays a critical role in body weight maintenance and metabolic homeostasis.
This study demonstrating a FABP4-UCP2 (show UCP2 ELISA Kits) axis with the potential to modulate the microglial inflammatory response.
our data establish A-FABP as a new molecular sensor in triggering macrophage-associated (show CD163 ELISA Kits) sterile inflammation in obesity.
these data offer a novel pathway whereby FABP4/aP2 regulates macrophage redox signaling and inflammasome activation via control of UCP2 (show UCP2 ELISA Kits) expression.
FABP4 locally produced by epicardial/perivascular fat and macrophages in vascular plaques contributes to the development of coronary atherosclerosis.
endothelial PATZ1 thus potently inhibits endothelial function and angiogenesis via inhibition of FABP4 expression, and abnormal induction of endothelial PATZ1 may contribute to multiple aspects of vascular dysfunction in diabetes
These results suggest that the antiinflammatory phenotype of FABP4/aP2 null mice is mediated by increased intracellular monounsaturated fatty acids leading to the increased expression of both uncoupling protein 2 (show UCP2 ELISA Kits) and SirT3 (show SIRT3 ELISA Kits).
FABP4 encodes the fatty acid binding protein found in adipocytes. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism.
adipocyte lipid-binding protein
, adipocyte-type fatty acid-binding protein
, fatty acid-binding protein 4
, fatty acid-binding protein, adipocyte
, fatty acid binding protein 4, adipocyte
, adipocyte fatty acid binding protein
, adipocyte-type fatty acid binding protein
, fatty acid binding protein 11
, fatty acid-binding protein H6
, peripheral myelin protein 2
, Adipocyte-type fatty acid-binding protein
, adipocyte fatty acid-binding protein 4
, Fatty acid-binding protein, adipocyte
, 3T3-L1 lipid-binding protein
, P2 adipocyte protein
, adipocyte protein aP2
, myelin P2 protein homolog
, protein 422