GCDH Protein (His tag)
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- 抗原 See all GCDH 蛋白
- GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- 大肠杆菌（E. Coli）
- 标记
- This GCDH protein is labelled with His tag.
- 原理
- Recombinant Human GCDH Protein (His Tag)
- 序列
- Arg45-Lys438
- 产品特性
- Recombinant Human Glutaryl-CoA Dehydrogenase, Mitochondrial is produced by our E.coli expression system and the target gene encoding Arg45-Lys438 is expressed with a 6His tag at the N-terminus.
- 纯度
- > 95 % as determined by reducing SDS-PAGE.
- 内毒素水平
- < 1.0 EU per μg as determined by the LAL method.
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- Discover our top product GCDH 蛋白
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Glutaryl-CoA Dehydrogenase (GCDH) (AA 45-438) protein (His tag)
GCDH 宿主: 人 宿主: 大肠杆菌（E. Coli） Recombinant Greater than 95 % as determined by SDS-PAGE WB, ELISA
Glutaryl-CoA Dehydrogenase (GCDH) (AA 1-438) protein (GST tag)GCDH 宿主: 人 宿主: 小麦胚 Recombinant WB, ELISA, AA, AP
Glutaryl-CoA Dehydrogenase (GCDH) (Transcript Variant 1) protein (Myc-DYKDDDDK Tag)GCDH 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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- 限制
- 仅限研究用
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- 状态
- Frozen, Liquid
- 缓冲液
- Supplied as a 0.2 μm filtered solution of 20 mM HEPES, 150 mM NaCl, pH 7.4.
- 储存条件
- -20 °C
- 储存方法
- Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
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- 抗原
- GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
- 别名
- GCDH (GCDH 产品)
- 别名
- ACAD5 Protein, GCD Protein, zgc:56505 Protein, zgc:77704 Protein, 9030411L18 Protein, AI266902 Protein, D17825 Protein, glutaryl-CoA dehydrogenase Protein, glutaryl-CoA dehydrogenase a Protein, glutaryl-Coenzyme A dehydrogenase Protein, GCDH Protein, Gcdh Protein, gcdha Protein
- 背景
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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.
Synonym: Glutaryl-CoA Dehydrogenase Mitochondrial, GCD, GCDH
- 分子量
- 45.0 kDa
- UniProt
- Q92947
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