关键信息
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基因名
MRPS9
- 应用
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别名
28S ribosomal protein S9; 28S ribosomal protein S9 mitochondrial; 28S ribosomal protein S9 mitochondrial precursor; mitochondrial; mitochondrial ribosomal protein S9; MRP S9; MRP-S9; MRPS9; RPMS9; RT09_HUMAN; S9mt
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种属
Human
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表达系统
E. coli
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标签
GST-tag at N-terminal
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
P82933
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表达区间
1-396 aa
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氨基酸序列
MAAPCVSYGGAVSYRLLLWGRGSLARKQGLWKTAAPELQTNVRSQILRLRHTAFVIPKKNVPTSKRETYTEDFIKKQIEEFNIGKRHLANMMGEDPETFTQEDIDRAIAYLFPSGLFEKRARPVMKHPEQIFPRQRAIQWGEDGRPFHYLFYTGKQSYYSLMHDVYGMLLNLEKHQSHLQAKSLLPEKTVTRDVIGSRWLIKEELEEMLVEKLSDLDYMQFIRLLEKLLTSQCGAAEEEFVQRFRRSVTLESKKQLIEPVQYDEQGMAFSKSEGKRKTAKAEAIVYKHGSGRIKVNGIDYQLYFPITQDREQLMFPFHFVDRLGKHDVTCTVSGGGRSAQAGAIRLAMAKALCSFVTEDEVEWMRQAGLLTTDPRVRERKKPGQEGARRKFTWKKR
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分子量
72.2 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.
质检流程
相关产品
背景信息
MRPS9, or Mitochondrial Ribosomal Protein S9, is a vital component of the mitochondrial ribosome, which plays a critical role in protein synthesis within mitochondrial organelles. Its significance has gained attention due to its involvement in various biological processes, including mitochondrial biogenesis, cellular metabolism, and the regulation of apoptosis. Mutations or dysregulation of MRPS9 have been linked to several mitochondrial diseases and may contribute to the pathogenesis of neurodegenerative disorders. Understanding the structure and function of MRPS9 is essential for elucidating its role in mitochondrial function and overall cellular health. Recent studies have utilized recombinant protein technology to produce MRPS9, enabling researchers to investigate its biochemical properties, interaction with mitochondrial RNA, and its impact on mitochondrial translation. This research is not only crucial for uncovering the molecular mechanisms of mitochondrial-related diseases but also holds potential for developing targeted therapeutic strategies aimed at restoring normal mitochondrial function. By elucidating the role of MRPS9 in the context of mitochondrial biology, scientists aim to contribute to the broader understanding of mitochondrial dysfunction and its implications in human health.
