产品货号：
JN1601
中文名称：
重组人ACOX1
英文名称：
Recombinant Human Peroxisomal Acyl-coenzyme A oxidase 1
产品规格：
10μg|50μg|500μg|1mg
发货周期：
1～3天
产品价格：
询价
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Leu660在N端含有His标签。
ACOX1质量控制：＞95%(还原性SDS-PAGE)
ACOX1制剂：液体
ACOX1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ACOX1：
Peroxisomal acyl-coenzyme A oxidase 1 is an enzyme belongs to the acyl-CoA oxidase family. It catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It shows highest activity against medium-chain fatty acyl-CoAs and activity decreases with increasing chain length.It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. it is involved in the pathway peroxisomal fatty acid beta-oxidation, which is part of Lipid metabolism. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids.
相关搜索：重组人ACOX1
ACOX1质量控制：＞95%(还原性SDS-PAGE)
ACOX1制剂：液体
ACOX1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于ACOX1：
Peroxisomal acyl-coenzyme A oxidase 1 is an enzyme belongs to the acyl-CoA oxidase family. It catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It shows highest activity against medium-chain fatty acyl-CoAs and activity decreases with increasing chain length.It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. it is involved in the pathway peroxisomal fatty acid beta-oxidation, which is part of Lipid metabolism. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids.
相关搜索：重组人ACOX1