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TPP1 Protein, Human, Recombinant (His)

产品编号 TMPY-02767

TPP1 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 60.7 kDa and the accession number is AAH14863.1.

TPP1 Protein, Human, Recombinant (His)

TPP1 Protein, Human, Recombinant (His)

产品编号 TMPY-02767
TPP1 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 60.7 kDa and the accession number is AAH14863.1.
规格价格库存数量
50 μg¥ 3,820¥ 2,215.6现货
100 μg¥ 6,5305日内发货
200 μg¥ 11,1305日内发货
500 μg¥ 22,5105日内发货
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生物活性

生物活性
Measured by the cleavage of AlaAlaPheAMC. The specific activity is > 850 pmoles/min/μg.
产品描述
TPP1 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 60.7 kDa and the accession number is AAH14863.1.
种属
Human
表达系统
Baculovirus Insect Cells
标签C-His
蛋白编号AAH14863.1
别名
tripeptidyl peptidase I,CLN2,TPP-1,SCAR7,GIG1,LPIC
蛋白构建
The pro form of Human TPP1 (AAH14863.1) (Met 1-Pro 563) was fused with a polyhistidine tag at the C-terminus.
蛋白纯度
> 95 % as determined by SDS-PAGE
TPP1 Protein, Human, Recombinant (His)
分子量60.7 kDa (predicted)
内毒素< 1.0 EU/μg of the protein as determined by the LAL method.
缓冲液Supplied as sterile 20 mM Tris, 500 mM NaCl, pH 7.4, 10% gly.
复溶方法
A Certificate of Analysis (CoA) containing reconstitution instructions is included with the products. Please refer to the CoA for detailed information.
存储
It is recommended to store the product under sterile conditions at -20°C to -80°C. Samples are stable for up to 12 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
运输方式In general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.
研究背景
Tripeptidyl-peptidase 1 (TPP1 / CLN2) is a member of the sedolisin family of serine proteases. The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity. It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification. TPP1 / CLN2 may act as a non-specific lysosomal peptidase which generates tripeptides from the breakdown products produced by lysosomal proteinases. Defects in TPP1 / CLN2 are the cause of neuronal ceroid lipofuscinosis type 2 (CLN2), a form of neuronal ceroid lipofuscinosis which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome. Neuronal ceroid lipofuscinoses are progressive neurodegenerative, lysosomal storage diseases characterized by intracellular accumulation of autofluorescent liposomal material, and clinically by seizures, dementia, visual loss, and/or cerebral atrophy.

计算器

  • 复溶 计算器
  • 重组蛋白稀释 计算器
  • 比活力 计算器

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