Analytical Data
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基因名
ADSL/Adenylosuccinate Lyase
- Application
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别名
AMPS; ASase; Adenylosuccinase
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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
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纯度
Greater than 95% as determined by SDS-PAGE.
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蛋白编号
P30566
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表达区间
Ala146~Leu484
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分子量
42kDa
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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
Adenylosuccinate lyase (ADSL) is a crucial enzyme involved in the purine nucleotide synthesis pathway, catalyzing the conversion of adenylosuccinate to adenine monophosphate (AMP) and fumarate. Mutations in the ADSL gene can lead to a rare but severe genetic disorder known as adenylosuccinate lyase deficiency, which is characterized by a range of neurological symptoms, intellectual disability, and developmental delays. The exploration of ADSL has garnered significant attention in biochemistry and molecular biology, particularly regarding the mechanisms underlying its enzymatic function and the repercussions of genetic mutations. The recombinant production of ADSL protein enables researchers to study its structure and function in depth, assess the effects of specific mutations, and explore potential therapeutic interventions. Characterizing the enzyme's kinetics and identifying inhibitors could yield insights into drug design for related metabolic disorders. Understanding ADSL not only sheds light on fundamental biochemical pathways but also has implications for the development of targeted therapies for patients afflicted with ADSL deficiency. As recombinant protein technology continues to evolve, ongoing research aims to enhance our understanding of this critical enzyme, paving the way for novel diagnostic and therapeutic strategies.












