Product Name
ACSL1, Polyclonal Antibody
Popular Item
Full Product Name
ACSL1 (Acyl-CoA Synthetase Long-chain Family Member 1, Acyl-CoA Synthetase 1, ACS1, FACL1, FACL2, LACS, Long-chain-fatty-acid-CoA Ligase 1, Long-chain Fatty Acid-CoA Ligase 2, Long-chain Acyl-CoA Synthetase 1, LACS 1, LACS1, Long-chain Acyl-CoA Synthetase
Product Synonym Names
Anti -ACSL1 (Acyl-CoA Synthetase Long-chain Family Member 1, Acyl-CoA Synthetase 1, ACS1, FACL1, FACL2, LACS, Long-chain-fatty-acid-CoA Ligase 1, Long-chain Fatty Acid-CoA Ligase 2, Long-chain Acyl-CoA Synthetase 1, LACS 1, LACS1, Long-chain Acyl-CoA Synthetase
Product Gene Name
anti-ACSL1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Chromosome Location
Chromosome: 4; NC_000004.11 (185676749..185747215, complement). Location: 4q35
3D Structure
ModBase 3D Structure for P33121
Species Reactivity
Human, Mouse, Rat
Specificity
Recognizes endogenous levels of human total ACSL1 protein. Species Crossreactivity: Mouse and rat.
Purity/Purification
Affinity Purified
Purified by peptide affinity chromatography.
Form/Format
Supplied as a liquid in 10mM sodium HEPES pH 7.5, 150mM NaCl, 0.1mg/ml BSA, 50% glycerol.
Immunogen
Synthetic peptide derived from a sequence of human ACSL1.
Preparation and Storage
May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of anti-ACSL1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-ACSL1 antibody
Mammalian long-chain acyl-CoA synthetase (ACSL) catalyzes the ligation of the fatty acid to CoA to form fatty acyl-CoA in a two-step reaction (1). Five isoforms of ACSL have been identified (1). These isoforms have different substrate preferences and subcellular localizations (1). Overexpression of ACSL1 results in changes of fatty acid metabolism in rat primary hepatocytes (2).
Product Categories/Family for anti-ACSL1 antibody
Antibodies; Abs to Enzymes, Synthetase
Applications Tested/Suitable for anti-ACSL1 antibody
Western Blot (WB), Immunohistochemistry (IHC)
Application Notes for anti-ACSL1 antibody
Suitable for use in Western Blot and Immunohistochemistry (Paraffin).
Dilution: Western Blot: 1:1000
Immunohistochemistry: 1:25
NCBI/Uniprot data below describe general gene information for ACSL1. It may not necessarily be applicable to this product.
UniProt Primary Accession #
P33121
[Other Products]
UniProt Secondary Accession #
P41215; Q8N8V7; Q8TA99; D3DP57[Other Products]
UniProt Related Accession #
P33121; Q108N1; Q108N2[Other Products]
Molecular Weight
77,943 Da[Similar Products]
NCBI Official Full Name
ACSL1 protein
NCBI Official Synonym Full Names
acyl-CoA synthetase long-chain family member 1
NCBI Official Symbol
ACSL1??[Similar Products]
NCBI Official Synonym Symbols
ACS1; LACS; FACL1; FACL2; LACS1; LACS2
??[Similar Products]
NCBI Protein Information
long-chain-fatty-acid--CoA ligase 1; LACS 1; LACS 2; OTTHUMP00000218456; OTTHUMP00000218457; OTTHUMP00000218460; OTTHUMP00000218461; OTTHUMP00000218462; OTTHUMP00000218465; acyl-CoA synthetase 1; palmitoyl-CoA ligase 1; palmitoyl-CoA ligase 2; paltimoyl-CoA ligase 1; 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; fatty-acid-Coenzyme A ligase, long-chain 1; fatty-acid-Coenzyme A ligase, long-chain 2
UniProt Protein Name
Long-chain-fatty-acid--CoA ligase 1
UniProt Synonym Protein Names
Acyl-CoA synthetase 1; ACS1; Long-chain acyl-CoA synthetase 1; LACS 1; Long-chain acyl-CoA synthetase 2; LACS 2; Long-chain fatty acid-CoA ligase 2; Palmitoyl-CoA ligase 1; Palmitoyl-CoA ligase 2
Protein Family
Long-chain-fatty-acid--CoA ligase
UniProt Gene Name
ACSL1??[Similar Products]
UniProt Synonym Gene Names
FACL1; FACL2; LACS; LACS1; LACS2??[Similar Products]
UniProt Entry Name
ACSL1_HUMAN
NCBI Summary for ACSL1
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. [provided by RefSeq]
UniProt Comments for ACSL1
ACSL1: Activation of long-chain fatty acids for both synthesis of cellular lipids, and degradation via beta-oxidation. Preferentially uses palmitoleate, oleate and linoleate. Highly expressed in liver, heart, skeletal muscle, kidney and erythroid cells, and to a lesser extent in brain, lung, placenta and pancreas. Belongs to the ATP-dependent AMP-binding enzyme family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: EC 6.2.1.3; Ligase; Membrane protein, integral; Lipid Metabolism - fatty acid
Chromosomal Location of Human Ortholog: 4q35.1
Cellular Component: peroxisomal membrane; mitochondrial outer membrane; endoplasmic reticulum membrane; membrane; mitochondrion; plasma membrane; integral to membrane
Molecular Function: ATP binding; long-chain-fatty-acid-CoA ligase activity
Biological Process: response to drug; response to oleate; unsaturated fatty acid metabolic process; lipid biosynthetic process; linoleic acid metabolic process; adiponectin-mediated signaling pathway; triacylglycerol biosynthetic process; cellular lipid metabolic process; long-chain fatty acid metabolic process; response to organic cyclic substance; response to nutrient; xenobiotic catabolic process
Research Articles on ACSL1
1. Data show that ACSL1 rs9997745 polymorphism influences metabolic syndrome risk, most likely via disturbances in fatty acid metabolism, which was modulated by dietary fat consumption, particularly PUFA intake, suggesting novel gene-nutrient interactions.
Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.