GTX89135-PEP
ACOX2 (Human) blocking peptide
Cannot supply to this region.
- SKU:
- GTX89135-PEP
- Additional Names:
- Acyl-Coa Oxidase 2 , Bcox , Brcacox , Brcox , Cbas6 , Thccox , Acox2
- Physical State:
- Lyophilized
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Buffer:
- Reconstitute with 200ul distilled water to obtain a 0.5mg/ml peptide solution. Lyophilized from 5% (v/v) acetonitrile/H₂O, no preservatives.
- Immunogen:
- acyl-CoA oxidase 2, branched chain
- Species:
- Human
- Synonyms:
- 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase;3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase;acyl-CoA oxidase 2, branched chain;acyl-Coenzyme A oxidase 2, branched chain;BCOX;branched chain acyl-CoA oxidase;BRCACOX;BRCOX;CBAS6;peroxisomal acyl-coenzyme A oxidase 2;peroxisomal branched chain acyl-CoA oxidase;THCA-CoA oxidase;THCCox;trihydroxycoprostanoyl-CoA oxidase
- Extra Details:
- The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children. [provided by RefSeq, Mar 2009]
- Shipping Conditions:
- Blue Ice