Analytical Data
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基因名
PARK7/DJ-1
- Application
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别名
Oncogene DJ1 Parkinson disease protein 7
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种属
Human
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表达系统
E. coli
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标签
N- His-GST
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q99497
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表达区间
1-174aa
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分子量
48.3 kDa
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
APT-1, also known as LYPLA1, is a member of the phospholipase family, specifically classified as a lysophospholipase. Research into APT-1/LYPLA1 has gained traction due to its potential implications in various physiological and pathological processes, including inflammation, cancer, and neurodegenerative diseases. The enzyme plays a critical role in the metabolism of lysophospholipids, which are bioactive lipids involved in cell signaling and membrane dynamics. Dysregulation of APT-1 activity has been linked to several disorders, prompting investigations into its biochemical properties and functional mechanisms. Recombinant APT-1/LYPLA1 protein production has enabled researchers to conduct detailed studies into its enzymatic activity, substrate specificity, and interactions with other cellular components. Understanding the structure and function of APT-1 not only contributes to fundamental lipid biology but also paves the way for the development of targeted therapeutic strategies that could potentially mitigate diseases associated with its dysfunction. The ongoing exploration of this enzyme may reveal novel metabolic pathways and therapeutic targets, highlighting its importance in biomedical research.
