Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4) Peptide
ACSL4
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN972849
Aperçu rapide pour Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4) Peptide (ABIN972849)
Antigène
ACSL4
(Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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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.
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Purification
- Purified
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
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Sujet
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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.
Alias Symbols: ACS4, FACL4, LACS4, MRX63, MRX68
Protein Size: 670 -
Poids moléculaire
- 74 kDa
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ID gène
- 2182
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NCBI Accession
- NM_004458, NP_004449
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UniProt
- O60488
Antigène
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