Analytical Data
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基因名
MRPS6
- Application
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别名
MRPS6; C21orf101; RPMS628S ribosomal protein S6; mitochondrial; MRP-S6; S6mt; Mitochondrial small ribosomal subunit protein bS6m
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种属
Human
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表达系统
E. coli
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标签
N- GST
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
P82932
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表达区间
1-125aa
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分子量
41.1 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
Related Products
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Protein Description
MRPS6, a member of the mitochondrial ribosomal protein family, plays a pivotal role in mitochondrial translation and is crucial for the proper assembly of mitochondrial ribosomes. Research on MRPS6 has gained attention due to its involvement in various cellular processes and its potential implications in mitochondrial dysfunction, which is often linked to a range of diseases, including neurodegenerative disorders and certain types of cancer. The protein is integral in the synthesis of mitochondrial-encoded proteins that are essential for oxidative phosphorylation, the process by which cells generate ATP. Consequently, mutations or aberrations in MRPS6 can lead to compromised mitochondrial function, highlighting its importance in cellular metabolism. Further studies are needed to elucidate the specific mechanisms by which MRPS6 influences mitochondrial activity and its role in disease pathology, making it a crucial target for research aimed at understanding mitochondrial biology and developing therapeutic strategies for mitochondrial-related disorders. This research could pave the way for potential interventions that restore mitochondrial function or target the specific pathways affected by MRPS6 alterations, ultimately contributing to improved therapeutic outcomes in associated diseases.
