产品信息
别名 | Dihydrolipoyl dehydrogenase (DLD); also called Dihydrolipoamide dehydrogenase; Glycine cleavage system L Protein; GCSL; LAD and PHE3; |
物种 | Mouse |
表达宿主 | Human Cells |
序列信息 | Ile26-Arg233 |
检索号 | P16382 |
分子量 | 51.5 kDa |
表观分子量 | 65-80 kDa |
生物活性 | Immobilized Mouse IL-4RA-Fc at 2μg/ml (100 μl/well)can bind Mouse IL-4-His.The ED50 of Mouse IL-4-His is 4.32 ng/ml. |
产品特性
纯度 | >95% as determined by reducing SDS-PAGE. |
内毒素 | <1.0 EU per µg as determined by LAL test. |
保存 | Lyophilized protein should be stored at -5~-20℃, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at -5~-20℃ for 3 months. |
运输 | Ambient temperature or ice pack. |
制剂 | Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4. |
复融 | Always centrifuge tubes before opening. Do not mix by vortex or pipetting.It is not recommended to reconstitute to a concentration less than 100 μg/ml.Dissolve the lyophilized protein in distilled water.Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
背景介绍
is a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. DLD exists as a homodimer. DLD is involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction. Mutations in its encoding gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.
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