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- 详细信息
- 技术资料
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- 规格:
1mg/500ug/50ug/10ug
| 规格: | 1mg | 产品价格: | ¥10080.0 |
|---|---|---|---|
| 规格: | 500ug | 产品价格: | ¥6912.0 |
| 规格: | 50ug | 产品价格: | ¥1560.0 |
| 规格: | 10ug | 产品价格: | ¥520.0 |
| 基本信息 | |
| 基因名 | |
| 别名 | Methylmalonyl-CoA epimerase;mitochondrial;DL-methylmalonyl-CoA racemase |
| 中文名称 | Recombinant Human Methylmalonyl-CoA epimerase/MCEE |
| 外观(性状) | Supplied as a 0.2 μm filtered solution of 20mM TrisHCl,150mM NaCl,1mM DTT,10%Glycerol,pH7.5. |
| 纯度 | ≥95% as determined by reducing SDS-PAGE. |
| 储存条件 | Store at≤-70℃,6 months.with seal;3 month after opening.Avoid freeze/thaw cycles. |
| 运输条件 | 干冰运输 |
| 背景说明 | Methylmalonyl-CoA epimerase,mitochondrial(MCEE)is an enzyme which belongs to the glyoxalase I family.It converts (S)-methylmalonyl-CoA to the (R) form,catalyses the following chemical reaction: (R)-methylmalonyl-CoA (S)-methylmalonyl-CoA.It plays an important role in the catabolism of fatty acids with odd-length carbon chains.This protein deficiency is an autosomal recessive inborn error of AA metabolism,involving valine,threonine,isoleucine and methionine.This organic aciduria can appear in the neonatal period with life-threatening metabolic acidosis,hyperammonemia,feeding difficulties,pancytopenia and coma. |
| 来源 | Human Cells |
| 内毒素 | Less than 0.1 ng/ug(1 EU/ug)as determined by LAL test. |
| 单位 | 支 |
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P00428 Recombinant Human Methylmalonyl-CoA epimerase/MCEE 细胞因子/蛋白
¥520 - 10080





