Analytical Data
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基因名
SLCO1B2
- Application
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别名
Oatp1b2; Slc21a10; SLC21A6; LST-1; Liver-Specific Organic Anion Transporter 1; Solute Carrier Family 21 Member 10
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种属
Mouse
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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 90% as determined by SDS-PAGE.
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蛋白编号
Q9JJL3
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表达区间
Phe421~Tyr533
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分子量
16kDa
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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
SLCO1B2, a member of the solute carrier organic anion transporter family, plays a crucial role in the hepatic uptake of various endogenous compounds and pharmaceuticals, including statins and anti-cancer drugs. Given its significant influence on drug pharmacokinetics and safety, understanding the function and regulation of SLCO1B2 has become a key focus in both pharmacology and toxicology research. Dysregulation or genetic polymorphisms in SLCO1B2 can lead to altered drug metabolism and interindividual variability in drug response, which may increase the risk of adverse effects or therapeutic failure. Recent advances in recombinant protein technology have enabled researchers to produce and study SLCO1B2 in vitro, facilitating a more detailed examination of its substrate specificity, transport mechanisms, and potential interactions with various inhibitors. Investigating the structural and functional characteristics of SLCO1B2 through reconstitution into artificial membranes provides insights that can aid in predicting drug-drug interactions and optimizing therapeutic regimens. The findings from such studies may ultimately contribute to personalized medicine approaches, informing clinicians about the best drug choices and dosages for individual patients based on their SLCO1B2 genotype and expression levels. Therefore, continuous research on SLCO1B2 recombinant proteins holds promise for enhancing our understanding of drug transport processes and improving clinical outcomes in the management of diseases treated with various pharmacotherapeutics.












