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Human Polyclonal Acsl1 Primary Antibody for WB - ABIN1881044
Phillips, Goumidi, Bertrais, Field, Cupples, Ordovas, Defoort, Lovegrove, Drevon, Gibney, Blaak, Kiec-Wilk, Karlstrom, Lopez-Miranda, McManus, Hercberg, Lairon, Planells, Roche: Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome. in Journal of lipid research 2010
Show all 3 Pubmed References
Human Monoclonal Acsl1 Primary Antibody for ELISA, WB - ABIN515508
Sandoval, Fraisl, Arias-Barrau, Dirusso, Singer, Sealls, Black: Fatty acid transport and activation and the expression patterns of genes involved in fatty acid trafficking. in Archives of biochemistry and biophysics 2008
Show all 2 Pubmed References
Human Polyclonal Acsl1 Primary Antibody for ICC, IF - ABIN314171
Fernando, Wiktorowicz, Soman, Kaphalia, Khan, Shakeel Ansari: Liver proteomics in progressive alcoholic steatosis. in Toxicology and applied pharmacology 2013
Cow (Bovine) Polyclonal Acsl1 Primary Antibody for IHC, WB - ABIN2777590
Ghosh, Barbosa, Singh: Molecular cloning and sequencing of human palmitoyl-CoA ligase and its tissue specific expression. in Molecular and cellular biochemistry 1996
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Cow (Bovine) Polyclonal Acsl1 Primary Antibody for IHC, WB - ABIN2777591
Soupene, Kuypers: Multiple erythroid isoforms of human long-chain acyl-CoA synthetases are produced by switch of the fatty acid gate domains. in BMC molecular biology 2006
These results suggest that ACSL1, ACSL4 (show ACSL4 Antibodies) and ACSL5 (show ACSL5 Antibodies) expression is regulated by ER signaling pathways and ACSL5 (show ACSL5 Antibodies) is a potential novel biomarker for predicting prognosis of breast cancer patients.
Study identified a genetic variant in the 3'-UTR (show UTS2R Antibodies) region of ACSL1 gene (rs8086) that may play a significant role in predicting outcomes of stage II/III patients with colon cancer, so that patients with T/T genotype had a significantly higher risk of tumor recurrence than those carrying at least one C allele.
The mRNA levels of ACSL1 were positively associated with those of HBXIP (show HBXIP Antibodies) in clinical breast cancer tissues. Thus, we conclude that the oncoprotein HBXIP (show HBXIP Antibodies) is able to up-regulate ACSL1 through activating the transcriptional factor Sp1 (show PSG1 Antibodies) in breast cancer.
evidence in humans of ACSL1 SNPs associated with fasting glucose, diabetes, and subclinical atherosclerosis
SRE motif in ACSL1 is essential for SREBP2 (show SREBF2 Antibodies)-mediated activation of C-ACSL1 gene transcription.
ACSL1 is a programmable mediator of insulin (show INS Antibodies) sensitivity and cellular lipid content.
the cell surface protein (show CD28 Antibodies) CD36 (show CD36 Antibodies)/FAT directly facilitates fatty acid transport across the plasma membrane, whereas the intracellular acyl-CoA (show GNPAT Antibodies) synthetases FATP4 (show SLC27A4 Antibodies) and ACSL1 enhance fatty acid uptake indirectly by metabolic trapping
Data indicate that expression of miR-205 is negatively related to that of ACSL1 in clinical hepatocellular carcinoma (HCC) tissues.
INSR rs1366600, ACSL1 rs2292899 and FABP2 rs11724758 could influence the susceptibility to type 2 diabetes in Chinese Han population, most likely through their effects on the specific miRNA-binding sites.
long-chain acyl-CoA synthetase 1 has a role in eicosapentaenoic acid suppression of palmitate-induced cytokine production
ACSL1-mediated metabolic trapping of exogenous LCFA accelerates LCFA uptake rates, albeit to a lesser extent in females, which distinctly affects LCFA trafficking to acyl intermediates but not triglyceride storage or mitochondrial oxidation and is affected by female sex hormones.
Data (including data from studies in cell line from knockout mice) suggest high incorporation of long-chain fatty acids, partly mediated by Acsl1, plays role in supply of octanoic acid for ghrelin (show GHRL Antibodies) acylation/lipoylation in ghrelin (show GHRL Antibodies)-producing cells.
Acyl-CoA synthetase 1 deficiency alters cardiolipin species and impairs mitochondrial function
long-chain acyl-CoA synthetase (show Acsl3 Antibodies) isoform 1 (ACSL1) deficiency in the heart activated mTORC1, thereby inhibiting autophagy and increasing the number of damaged mitochondria.
Acsl1(M-/-) mice were more insulin (show INS Antibodies) sensitive, and, during an overnight fast, their respiratory exchange ratio was higher, indicating greater glucose use and during endurance exercise, Acsl1(M-/-) mice ran only 48% as far as controls.
These data indicate that Acsl1-deficiency causes diastolic dysfunction and that mTOR (show FRAP1 Antibodies) activation is linked to the development of cardiac hypertrophy in Acsl1(H-/-) mice.
Data indicate that the expression levels of ACSL1 and its metabolite triglyceride levels were remarkably increased in hepatitis B virus X protein (HBx)-induced liver cancer tissues from the HBx transgenic mice model.
Increases understanding of the role of ACSL1 in monocytes/macrophages in inflammation and diabetes-accelerated atherosclerosis offers hope for new treatment to combat diabetic vascular disease[review]
Acyl-CoA synthetase 1 is induced by Gram-negative bacteria and lipopolysaccharide and is required for phospholipid turnover in stimulated macrophages
The pig ACSL1 gene expresses differently in different tissues and pig breeds.
Authors have sequenced 3,013 bp of the pig acyl coenzyme A (show SOAT1 Antibodies) long-chain synthetase 1 (ACSL1) gene.
The initial QTL analysis suggested the ACSL1 gene as a candidate gene for fatty acid composition in bovine skeletal muscle; subsequent analyses indicate that ACSL1 or a gene in close proximity plays a functional role in the lipid composition of beef.
The results of this study suggest that suggest that SLC27A6 (show SLC27A6 Antibodies), ACSL1, FABP3 (show FABP3 Antibodies), AGPAT6 (show AGPAT6 Antibodies), and LPIN1 (show LPIN1 Antibodies) coordinately regulate the channeling of fatty acids toward copious milk fat synthesis in bovine mammary.
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation.
, LACS 2
, acyl-CoA synthetase 1
, fatty-acid-Coenzyme A ligase, long-chain 1
, fatty-acid-Coenzyme A ligase, long-chain 2
, lignoceroyl-CoA synthase
, long-chain acyl-CoA synthetase 1
, long-chain acyl-CoA synthetase 2
, long-chain fatty acid-CoA ligase 2
, long-chain fatty-acid-coenzyme A ligase 1
, long-chain-fatty-acid--CoA ligase 1
, palmitoyl-CoA ligase 1
, palmitoyl-CoA ligase 2
, paltimoyl-CoA ligase 1
, acetate-CoA ligase
, acetyl-CoA synthetase
, acetyl-Coenzyme A synthetase 1 (ADP forming)
, fatty acid Coenzyme A ligase, long chain 2
, Acyl CoA synthetase, long chain
, long-chain-fatty-acid--CoA ligase, liver isozyme
, acyl coenzyme A synthetase long-chain 1
, fatty acid coenzyme A ligase long-chain 2
, palmitoyl-CoA ligase