Analytical Data
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基因名
MIPOL1
- Application
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别名
MIPOL1Mirror-image polydactyly gene 1 protein
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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
Q8TD10
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表达区间
1-442 aa
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氨基酸序列
MENWSKDITH SYLEQETTGI NKSTQPDEQL TMNSEKSMHR KSTELVNEIT CENTEWPGQR STNFQIISSY PDDESVYCTT EKYNVMEHRH NDMHYECMTP CQVTSDSDKE KTIAFLLKEL DILRTSNKKL QQKLAKEDKE QRKLKFKLEL QEKETEAKIA EKTAALVEEV YFAQKERDEA VMSRLQLAIE ERDEAIARAK HMEMSLKVLE NINPEENDMT LQELLNRINN ADTGIAIQKN GAIIVDRIYK TKECKMRITA EEMSALIEER DAALSKCKRL EQELHHVKEQ NQTSANNMRH LTAENNQERA LKAKLLSMQQ ARETAVQQYK KLEEEIQTLR VYYSLHKSLS QEENLKDQFN YTLSTYEEAL KNRENIVSIT QQQNEELATQ LQQALTERAN MELQLQHARE ASQVANEKVQ KLERLVDVLR KKVGTGTMRT VI
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分子量
51.5 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
MIPOL1, or "Mitochondrial protein involved in oxidative phosphorylation 1," is a protein of significant interest in cellular biology and mitochondrial research. It plays a critical role in maintaining mitochondrial function and dynamics, which are essential for energy production through ATP synthesis. Mitochondrial dysfunction is implicated in various diseases, including neurodegenerative disorders, cardiovascular diseases, and metabolic syndromes. Recent studies have suggested that MIPOL1 is involved in the regulation of mitochondrial morphology, facilitating the balance between mitochondrial fission and fusion. Such processes are crucial for mitochondrial health and cellular metabolism. Researchers have been investigating the functional pathways of MIPOL1, delving into its potential mechanisms of action in modulating mitochondrial dynamics and how it interacts with other key proteins involved in these processes. Furthermore, understanding the role of MIPOL1 could illuminate novel therapeutic targets for diseases characterized by mitochondrial abnormalities. Thus, the recombinant study of MIPOL1 not only enhances our understanding of mitochondrial biology but also paves the way for potential interventions in mitochondrial-linked diseases.
