ACADL anticorps (N-Term)
Aperçu rapide pour ACADL anticorps (N-Term) (ABIN2778158)
Antigène
Voir toutes ACADL AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- N-Term
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Fonction
- ACADL Antibody - N-terminal region
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Séquence
- MAARLLRGSL RVLGGHRAPR QLPAARCSHS GGEERLETPS AKKLTDIGIR
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Homologie
- Cow: 93%, Dog: 86%, Horse: 100%, Human: 100%, Mouse: 92%, Pig: 93%, Rabbit: 85%, Rat: 92%
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Attributs du produit
- This is a rabbit polyclonal antibody against ACADL. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the N terminal region of human ACADL
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under ABIN8093963
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
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Autre désignation
- ACADL
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Sujet
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Background Information: ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in ACADL gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
Gene Name: Acyl-CoA dehydrogenase, long chain
Alternative Symbols: LCAD, ACAD4
Protein Name: Long-chain specific acyl-CoA dehydrogenase, mitochondrial
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Poids moléculaire
- 44kDa
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ID gène
- 33
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NCBI Accession
- NP_001599
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UniProt
- P28330
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Pathways
- Monocarboxylic Acid Catabolic Process
Antigène
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