ACSL4
(Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
Attributs du produit
This is a synthetic peptide designed for use in combination with anti-ACSL4 antibody (Catalog #: ARP49774_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Each Investigator should determine their own optimal working dilution for specific applications.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Concentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Conseil sur la manipulation
Avoid repeated freeze-thaw cycles.
Stock
-20 °C
Stockage commentaire
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Antigène
ACSL4
(Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
Synonymes
acsl4 Peptide, zgc:66186 Peptide, ACSL4 Peptide, ACS4 Peptide, FACL4 Peptide, LACS4 Peptide, MRX63 Peptide, MRX68 Peptide, 9430020A05Rik Peptide, AU018108 Peptide, Facl4 Peptide, Lacs4 Peptide, Acs4 Peptide, acs4 Peptide, acsl3 Peptide, facl4 Peptide, lacs4 Peptide, mrx63 Peptide, mrx68 Peptide, T32A16.20 Peptide, T32A16_20 Peptide, long-chain acyl-CoA synthetase 4 Peptide, acyl-CoA synthetase long chain family member 4a Peptide, acyl-CoA synthetase long-chain family member 4 Peptide, acyl-CoA synthetase long chain family member 4 Peptide, AcsL4 Peptide, acyl-CoA synthetase long chain family member 3 Peptide, Long-chain-fatty-acid--CoA ligase 4 Peptide, acyl-CoA synthetase long-chain family member 4 S homeolog Peptide, AMP-dependent synthetase and ligase family protein Peptide, acsl4a Peptide, ACSL4 Peptide, acsL4 Peptide, acsl3 Peptide, acsl4 Peptide, Acsl4 Peptide, acsl4.S Peptide, LACS4 Peptide
Sujet
ACSL4 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. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants.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. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants.