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产品名称
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单价(含增值税)
库存(PCS)
起订数量
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,48T¥ 16001
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,96T¥ 26001
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,GV-P01250-10ug¥ 1176.001
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,GV-P01250-50ug¥ 3720.001
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,GV-P01250-500ug¥ 13520.001
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Recombinant Human GCDH/Glutaryl-CoA dehydrogenase,GV-P01250-1mg¥ 18800.001
产品简介
Known as | Glutaryl-CoA Dehydrogenase Mitochondrial; GCD; GCDH |
Derived from | E.coli |
Purity | Greater than 95% as determined by reducing SDS-PAGE. |
Formulation | Supplied as a 0.2 μm filtered solution of 20mM HEPES, 150mM NaCl, pH 7.4. |
Storage | Store at ≤-70°C, stable for 6 months after receipt.Store at ≤-70°C, stable for 3 months under sterile conditions after opening.Please minimize freeze-thaw cycles. |
Endotoxin | Less than 0.1 ng/ug (1 EU/ug) as determined by LAL test. |
Background | 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. |
规格 | 10ug50ug500ug1mg |
注意:
1.本产品仅供科研使用。请勿用于医药、临床诊断或治疗,食品及化妆品等用途。请勿存放于普通住宅区。
2.为了您的安全和健康,请穿好实验服并佩戴一次性手套和口罩操作。
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