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anti-Human FABP4 Antikörper:
anti-Mouse (Murine) FABP4 Antikörper:
anti-Rat (Rattus) FABP4 Antikörper:
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Human Polyclonal FABP4 Primary Antibody für ICC, IF - ABIN4309936
Zhao, Ren, Chen, Zhang, Cheng, Li, Zhang, Gao: Differential expression of lipid metabolism related genes in porcine muscle tissue leading to different intramuscular fat deposition. in Lipids 2010
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Human Monoclonal FABP4 Primary Antibody für ELISA, WB - ABIN969125
Smith, Sanders, Thompson, Londos, Kraemer, Bernlohr: Physical association between the adipocyte fatty acid-binding protein and hormone-sensitive lipase: a fluorescence resonance energy transfer analysis. in The Journal of biological chemistry 2004
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Human Monoclonal FABP4 Primary Antibody für ELISA, WB - ABIN969126
Tuncman, Erbay, Hom, De Vivo, Campos, Rimm, Hotamisligil: A genetic variant at the fatty acid-binding protein aP2 locus reduces the risk for hypertriglyceridemia, type 2 diabetes, and cardiovascular disease. in Proceedings of the National Academy of Sciences of the United States of America 2006
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Human Monoclonal FABP4 Primary Antibody für ELISA, WB - ABIN966115
Ohlsson, Moreira, Gromov, Sauter, Celis: Loss of expression of the adipocyte-type fatty acid-binding protein (A-FABP) is associated with progression of human urothelial carcinomas. in Molecular & cellular proteomics : MCP 2005
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Human Polyclonal FABP4 Primary Antibody für IF (p), IHC (p) - ABIN753223
Claycombe, Vomhof-DeKrey, Garcia, Johnson, Uthus, Roemmich et al.: Decreased beige adipocyte number and mitochondrial respiration coincide with increased histone methyl transferase (G9a) and reduced FGF21 gene expression in Sprague-Dawley rats fed prenatal low ... in The Journal of nutritional biochemistry 2016
Human Monoclonal FABP4 Primary Antibody für ELISA, WB - ABIN4270908
Pan, Tian, Park, Lofftus, Mei, Liu, Luo, OMalley, Gehad, Teague, Divito, Fuhlbrigge, Puigserver, Krueger, Hotamisligil, Clark, Kupper: Survival of tissue-resident memory T cells requires exogenous lipid uptake and metabolism. in Nature 2017
Human Monoclonal FABP4 Primary Antibody für WB - ABIN1882241
Baxa, Sha, Buelt, Smith, Matarese, Chinander, Boundy, Bernlohr: Human adipocyte lipid-binding protein: purification of the protein and cloning of its complementary DNA. in Biochemistry 1990
Mouse (Murine) Polyclonal FABP4 Primary Antibody für ICC, IHC - ABIN1078018
Li, Liang, Wu, Ma, Su: Valproate acid (VPA)-induced dysmetabolic function in clinical and animal studies. in Clinica chimica acta; international journal of clinical chemistry 2017
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 (zeige INS Antikörper) 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 (zeige INS Antikörper) 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.
Exogenous FABP4 plays a key role in tumor proliferation and activates the expression of fatty acid transport proteins in MCF-7 breast cancer cells.
High FABP4 expression is associated with Acute Monocytic Leukemia (zeige KAT6B Antikörper).
FABP4 over-expression in cardiomyocytes can aggravate the development of cardiac hypertrophy through the activation of ERK (zeige EPHB2 Antikörper) signal pathway.
Results show that serum FABP4 levels were significantly increased in patients with psoriasis.
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 (zeige CSN2 Antikörper) 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 (zeige NR1H3 Antikörper)), stearoyl-CoA desaturase (SCD (zeige SCD Antikörper)), Fatty acid synthase (FASN (zeige FASN Antikörper)), 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 (zeige FAT1 Antikörper) 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.
High Fabp4 expression is associated with Acute myeloid leukemia (zeige BCL11A Antikörper).
These data suggest that the function of SIRT6 (zeige SIRT6 Antikörper) 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 (zeige UCP2 Antikörper) axis with the potential to modulate the microglial inflammatory response.
our data establish A-FABP as a new molecular sensor in triggering macrophage-associated (zeige CD163 Antikörper) sterile inflammation in obesity.
these data offer a novel pathway whereby FABP4/aP2 regulates macrophage redox signaling and inflammasome activation via control of UCP2 (zeige UCP2 Antikörper) expression.
FABP4 locally produced by epicardial/perivascular fat and macrophages in vascular plaques contributes to the development of coronary atherosclerosis.
endothelial PATZ1 (zeige ZNF278 Antikörper) thus potently inhibits endothelial function and angiogenesis via inhibition of FABP4 expression, and abnormal induction of endothelial PATZ1 (zeige ZNF278 Antikörper) 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 (zeige UCP2 Antikörper) and SirT3 (zeige SIRT3 Antikörper).
FABP4 could reverse the activation of the leptin (zeige LEP Antikörper)-induced mitochondrial fatty acid oxidation.
FABP4 is a hypoxia inducible gene that sensitizes mice to liver I/R injury.
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