产品货号：
JN1026
中文名称：
重组人GCDH(线粒体戊二酰辅酶A脱氢酶)
英文名称：
Recombinant Human Glutaryl-CoA Dehydrogenase, Mitochondrial
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Arg45-Lys438在N端含有His标签。
GCDH质量控制：＞95%(还原性SDS-PAGE)
GCDH制剂：液体
GCDH保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于GCDH：
Glutaryl-CoA Dehydrogenase Mitochondrial (GCDH) is an enzyme that acts upon glutaryl-coenzyme A, creating crotonyl-coenzyme A. It plays a role in the metabolism of lysine, hydroxylysine and tryptophan. It uses electron transfer flavoprotein as its electron acceptor. Isoform Short is inactive Glutaryl-CoA and electron-transfer flavoprotein to (E)-but-2-enoyl-CoA, CO2 and reduced electron-transfer flavoprotein. A defect in this enzyme is associated with neurological condition glutaric acidemia type 1 and cause a progressive form of early-onset generalized dystonia.
相关搜索：重组人GCDH(线粒体戊二酰辅酶A脱氢酶)
GCDH质量控制：＞95%(还原性SDS-PAGE)
GCDH制剂：液体
GCDH保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于GCDH：
Glutaryl-CoA Dehydrogenase Mitochondrial (GCDH) is an enzyme that acts upon glutaryl-coenzyme A, creating crotonyl-coenzyme A. It plays a role in the metabolism of lysine, hydroxylysine and tryptophan. It uses electron transfer flavoprotein as its electron acceptor. Isoform Short is inactive Glutaryl-CoA and electron-transfer flavoprotein to (E)-but-2-enoyl-CoA, CO2 and reduced electron-transfer flavoprotein. A defect in this enzyme is associated with neurological condition glutaric acidemia type 1 and cause a progressive form of early-onset generalized dystonia.
相关搜索：重组人GCDH(线粒体戊二酰辅酶A脱氢酶)