ACSL4 Polyclonal Antibody (E-AB-14661)
For research use only.
Verified Samples |
Verified Samples in WB: HepG2, Hela, Human fetal kidney, Human liver Verified Samples in IHC: Human liver cancer, Human gastric cancer |
Dilution | WB 1:1000-1:5000, IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC |
Clonality | Polyclonal |
Immunogen | Recombinant protein of human ACSL4 |
Abbre | ACSL4 |
Synonyms | ACS 4, ACS4, ACSL 4, ACSL4, Acsl4, Acyl CoA synthetase long chain family member 4, FACL 4, FACL4, Fatty acid Coenzyme A ligase, LACS 4, LACS4, Lignoceroyl CoA synthase, Long chain 4, acyl CoA synthetase 4, fatty acid Coenzyme A ligase long-chain 4, long chain acyl CoA s |
Swissprot | |
Calculated MW | 79 kDa |
Cellular Localization | Mitochondrion outer membrane. Peroxisome membrane. Microsome membrane. Endoplasmic reticulum membrane. |
Concentration | 0.2 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Metabolism, Signal Transduction |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | 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. |
Other Clones
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Other Formats
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Unconjugated
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