Analytical Data
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基因名
MRPL15
- Application
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别名
MRPL19; KIAA0104; MRPL15; 39S ribosomal protein L19; mitochondrial; L19mt; MRP-L19; 39S ribosomal protein L15; mitochondrial; L15mt; MRP-L15; Mitochondrial large ribosomal subunit protein bL19m
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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
P49406
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表达区间
1-292 aa
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氨基酸序列
MAACIAAGHWAAMGLGRSFQAARTLLPPPASIACRVHAGPVRQQSTGPSEPGAFQPPPKPVIVDKHRPVEPERRFLSPEFIPRRGRTDPLKFQIERKDMLERRKVLHIPEFYVGSILRVTTADPYASGKISQFLGICIQRSGRGLGATFILRNVIEGQGVEICFELYNPRVQEIQVVKLEKRLDDSLLYLRDALPEYSTFDVNMKPVVQEPNQKVPVNELKVKMKPKPWSKRWERPNFNIKGIRFDLCLTEQQMKEAQKWNQPWLEFDMMREYDTSKIEAAIWKEIEASKRS
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分子量
60.5 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
MRPL15 (Mitochondrial Ribosomal Protein L15) is a vital component of the mitochondrial ribosome, playing a crucial role in protein synthesis within mitochondria. Due to its involvement in mitochondrial function, MRPL15 is essential for maintaining cellular energy levels and regulating metabolic processes. Dysregulation or mutations in MRPL15 have been implicated in various mitochondrial diseases, which can lead to severe health issues, including neuromuscular disorders and metabolic syndromes. Research on MRPL15 has gained significant attention in recent years as scientists aim to understand its structure, function, and the molecular mechanisms by which it contributes to mitochondrial integrity. Insights into MRPL15 may pave the way for therapeutic approaches targeting mitochondrial dysfunction, potentially offering new avenues for the treatment of related diseases. Additionally, MRPL15 serves as a model for studying the evolution of mitochondrial ribosomal proteins and their roles in the complex interplay of genetic expression and cellular metabolism. Overall, the study of MRPL15 is critical not only for elucidating mitochondrial biology but also for developing strategies to combat mitochondrial-related diseases.
