Analytical Data
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基因名
RHOT1
- Application
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别名
MIRO-1 Alternative name(s): Ras homolog gene family member T1
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种属
Chicken
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表达系统
E. coli
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标签
N- His-SUMO
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q5ZM73
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表达区间
1-219aa
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分子量
41 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
RHOT1, a member of the Ras superfamily of small GTPases, has garnered increasing attention due to its crucial role in cellular processes such as mitochondrial dynamics, cell migration, and proliferation. Initially identified for its function in regulating organelle movement within cells, RHOT1 has been implicated in various pathological conditions, including cancer and neurodegenerative diseases. Research has demonstrated that RHOT1 interacts with multiple proteins involved in mitochondrial transport and fusion, highlighting its significance in maintaining mitochondrial integrity and function. Additionally, its dysregulation has been associated with altered cellular metabolism and enhanced tumorigenic properties. Given these implications, there is a growing interest in developing recombinant RHOT1 protein for further characterization studies that aim to elucidate its biological functions and regulatory mechanisms. Understanding RHOT1 at a molecular level may unveil new therapeutic targets and strategies for diseases linked to mitochondrial dysfunction and aberrant cell signaling pathways. Therefore, the production and study of RHOT1 recombinant protein is not only fundamental for basic scientific research but also for advancing our knowledge in clinical applications related to cancer and other disorders involving mitochondrial dynamics.
