ACSL4 anticorps (AA 1-280)
Aperçu rapide pour ACSL4 anticorps (AA 1-280) (ABIN6136458)
Antigène
Voir toutes ACSL4 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1-280
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Séquence
- MAKRIKAKPT SDKPGSPYRS VTHFDSLAVI DIPGADTLDK LFDHAVSKFG KKDSLGTREI LSEENEMQPN GKVFKKLILG NYKWMNYLEV NRRVNNFGSG LTALGLKPKN TIAIFCETRA EWMIAAQTCF KYNFPLVTLY ATLGKEAVVH GLNESEASYL ITSVELLESK LKTALLDISC VKHIIYVDNK AINKAEYPEG FEIHSMQSVE ELGSNPENLG IPPSRPTPSD MAIVMYTSGS TGRPKGVMMH HSNLIAGMTG QCERIPGLGP KDTYIGYLPL
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Réactivité croisée
- Humain, Souris, Rat
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Attributs du produit
- Polyclonal Antibodies
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Purification
- Affinity purification
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Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-280 of human ACSL4 (NP_004449.1).
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Isotype
- IgG
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Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
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Commentaires
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HIGH QUALITY
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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: "Morphologically and Functionally Distinct Lipid Droplet Subpopulations." dans: Scientific reports, Vol. 6, pp. 29539, (2018) (PubMed).
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: "Morphologically and Functionally Distinct Lipid Droplet Subpopulations." dans: Scientific reports, Vol. 6, pp. 29539, (2018) (PubMed).
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- ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
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Autre désignation
- ACSL4
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Sujet
- 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 multiple transcript variants.,ACSL4,ACS4,FACL4,LACS4,MRX63,MRX68,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,ACSL4
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Poids moléculaire
- 74 kDa/79 kDa
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ID gène
- 2182
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UniProt
- O60488
Antigène
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