ACOX1 anticorps (AA 221-320)
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- Antigène Voir toutes ACOX1 Anticorps
- ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
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Épitope
- AA 221-320
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ACOX1 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Homologie
- Human,Mouse,Rat,Sheep,Pig,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human ACOX1
- Isotype
- IgG
- Top Product
- Discover our top product ACOX1 Anticorps primaire
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- Indications d'application
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
- Autre désignation
- ACOX1 (ACOX1 Produits)
- Synonymes
- anticorps zgc:92584, anticorps wu:fb59h12, anticorps zgc:114033, anticorps aco, anticorps acox, anticorps ACOX, anticorps PALMCOX, anticorps SCOX, anticorps RATACOA1, anticorps AOX, anticorps Acox, anticorps D130055E20Rik, anticorps Paox, anticorps PCOX1, anticorps acyl-CoA oxidase 1, anticorps acyl-CoA oxidase 1, palmitoyl, anticorps acyl-CoA oxidase 1, palmitoyl L homeolog, anticorps acyl-Coenzyme A oxidase 1, palmitoyl, anticorps ACOX1, anticorps acox1, anticorps acox1.L, anticorps Acox1
- Sujet
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Synonyms: ACOX1, ACOX1_HUMAN, AOX antibody Palmitoyl CoA oxidase, Palmitoyl-CoA oxidase, Peroxisomal acyl coenzyme A oxidase 1, Peroxisomal acyl-coenzyme A oxidase 1, SCOX, Straight chain acyl CoA oxidase, Straight-chain acyl-CoA oxidase.
Background: Defects in ACOX1 are the cause of adrenoleukodystrophy pseudoneonatal (Pseudo-NALD), also known as peroxisomal acyl-CoA oxidase deficiency. Pseudo-NALD is a peroxisomal single-enzyme disorder. Clinical features include mental retardation, leukodystrophy, seizures, mild hepatomegaly, hearing deficit. Pseudo-NALD is characterized by increased plasma levels of very-long chain fatty cids, due to decreased or absent peroxisome acyl-CoA oxidase activity. Peroxisomes are intact and functioning.
- ID gène
- 51
- Pathways
- Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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