Analytical Data
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基因名
ASAH2B
- Application
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别名
ASAH2B;ASAH2C;ASAH2L;Putative inactive neutral ceramidase B
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种属
Human
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表达系统
E. coli
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标签
His tag N-Terminus
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
P0C7U1
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表达区间
1-165aa
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氨基酸序列
MRQHRQFMDRTHYLLTFSSSETLLRLLLRIVDRAPKGRTFGDVLQPAKPEYRVGEVAEVIFVGANPKNSVQNQTHQTFLTVEKYEATSTSWQIVCNDASWETRFYWHKGLLGLSNATVEWHIPDTAQPGIYRIRYFGHNRKQDILKPAVILSFEGTSPAFEVVTI
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分子量
21.0 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
ASAH2B, a member of the N-acylsphingosine amidohydrolase family, plays a crucial role in sphingolipid metabolism by catalyzing the hydrolysis of sphingosine N-acyls in various biological processes. The study of ASAH2B has gained significance due to its involvement in diverse physiological functions and its potential implications in several diseases, including cancer, neurodegenerative disorders, and inflammation. Research indicates that alterations in the expression or activity of ASAH2B can lead to dysregulation of sphingolipid homeostasis, which is linked to the development of pathologies. Specifically, the enzyme's substrate specificity and its role in producing bioactive lipids have made it a target for therapeutic intervention. Understanding the mechanistic aspects of ASAH2B, including its structure, function, and regulatory pathways, is vital for elucidating its contribution to lipid signaling and metabolic regulation. Additionally, the generation of recombinant ASAH2B proteins allows for detailed biochemical studies, enabling researchers to explore its enzymatic properties and potential interactions with other molecules. This research not only enhances our understanding of sphingolipid metabolism but also opens avenues for developing novel therapeutic strategies aimed at modulating ASAH2B activity in disease contexts. Thus, the study of ASAH2B is at the forefront of lipid biochemistry and holds promise for advancing both basic research and clinical applications.












