Overview
Product nameACOX1 protein
Protein descriptionRecombinant full length (aa 1-660) Human ACOX1 (Q15067) with N-Terminal proprietary tag. Mol Wt 98.71 kDa inclusive of tag.
Uniprot accessionQ15067
Molecular weight98.710kDa inclusive of tags
Protein length660 amino acids
Expression hostWheat germ
Properties
FormLiquid
Storage instructionsShipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Storage bufferpH: 8.00
Constituents: 0.3% Glutathione, 0.79% Tris HCl
Concentration information loading...
Additional notesProtein concentration is above or equal to 0.05 mg/ml.
Best used within three months from the date of receipt.
Sequence notesMNPDLRRERDSASFNPELLTHILDGSPEKTRRRREIENMI LNDPDFQHEDLNFLTRSQRYEVAVRKSAIMVKKMREFGIA DPDEIMWFKNFVHRGRPEPLDLHLGMFLPTLLHQATAEQQ ERFFMPAWNLEIIGTYAQTEMGHGTHLRGLETIATYDPET QEFILNSPTVTSIKWWPGGLGKTSNHAIVLAQLITKGKCY GLHAFIVPIREIGTHKPLPGITVGDIGPKFGYDEIDNGYL KMDNHRIPRENMLMKYAQVKPDGTYVKPLSNKLTYGTMVF VRSFLVGEAARALSKACTIAIRYSAVRHQSEMKPGEPEPQ ILDFQTQQYKLFPLLATAYAFQFVGAYMKETYHRINEGIG QGDLSELPELHALTAGLKAFTSWTANTGIEACRMACGGHG YSHCSGLPNIYVNFTPSCTFEGENTVMMLQTARFLMKSYD QVHSGKLVCGMVSYLNDLPSQRIQPQQVAVWPTMVDINSP ESLTEAYKLRAARLVEIAAKNLQKEVIHRKSKEVAWNLTS VDLVRASEAHCHYVVVKLFSEKLLKIQDKAIQAVLRSLCL LYSLYGISQNAGDFLQGSIMTEPQITQVNQRVKELLTLIR SDAVALVDAFDFQDVTLGSVLGRYDGNVYENLFEWAKNSP LNKAEVHESYKHLKSLQSKL
Research Areas
Applications
Our Abpromise guarantee covers the use of
ab114556
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Application
|
Notes |
| ELISA |
ELISA: Use at an assay dependent concentration. |
| SDS-PAGE |
SDS-PAGE: Use at an assay dependent concentration. |
| WB |
WB: Use at an assay dependent concentration. |
Protein info
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Alternative names
EC 1.3.3.6Palmitoyl CoA oxidasePalmitoyl-CoA oxidasePeroxisomal acyl coenzyme A oxidase 1Peroxisomal acyl-coenzyme A oxidase 1SCOXStraight chain acyl CoA oxidaseStraight-chain acyl-CoA oxidase
see all
FunctionCatalyzes the desaturation of very long chain acyl-CoAs to 2-trans-enoyl-CoAs.
PathwayLipid metabolism; peroxisomal fatty acid beta-oxidation.
Involvement in diseaseDefects in ACOX1 are the cause of adrenoleukodystrophy pseudoneonatal (Pseudo-NALD) [MIM:264470]; 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.
Sequence similaritiesBelongs to the acyl-CoA oxidase family.
Cellular localizationPeroxisome.
References for ACOX1 protein (ab114556)
ab114556
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"