Analytical Data
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基因名
Beta-lactamase TEM/Bla
- Application
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别名
Carbapenem-hydrolyzing beta-lactamase KPC-2
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种属
Klebsiella oxytoca
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表达系统
E. coli
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标签
Tag Free
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q848S6
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表达区间
25-293aa
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分子量
28.6 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
Beta-lactamase TEM (also known as β-lactamase type TEM) is a critical enzyme that provides antibiotic resistance to bacteria, particularly against penicillin and other beta-lactam antibiotics. The emergence of TEM beta-lactamases represents a significant challenge in treating bacterial infections, as these enzymes can hydrolyze a broad spectrum of beta-lactam antibiotics, leading to treatment failure. TEM beta-lactamases are mostly found in Enterobacteriaceae and are often encoded by plasmids, facilitating rapid dissemination among bacterial populations. Research involving the recombinant expression of TEM/Bla proteins is vital for understanding the structure-function relationships of these enzymes, their resistance mechanisms, and the impact of mutations on enzymatic activity. Moreover, studying these proteins in a laboratory setting can inform the development of novel inhibitors and therapeutic strategies to combat antibiotic resistance. This has profound implications for public health, as the increasing prevalence of resistant strains complicates the management of infectious diseases. Therefore, ongoing research into the biochemical properties and genetic variants of TEM beta-lactamases is essential for advancing our knowledge of antibiotic resistance and enhancing the effectiveness of current and future antimicrobial therapies.












