Analytical Data
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Gene name
MRPS24
- Application
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Alternative Names
MRPS24; HSPC33528S ribosomal protein S24; mitochondrial; MRP-S24; S24mt; Mitochondrial small ribosomal subunit protein uS3m; bMRP-47; bMRP47
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Species
Human
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Source
E. coli
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Tag
His tag N-Terminus
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q96EL2
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Expression Region
36-167 aa
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AA Sequence
KNRAA RVRVSKGDKP VTYEEAHAPH YIAHRKGWLS LHTGNLDGED HAAERTVEDV FLRKFMWGTF PGCLADQLVL KRRGNQLEIC AVVLRQLSPH KYYFLVGYSE TLLSYFYKCP VRLHLQTVPS KVVYKYL
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Molecular Weight
19.0 kDa
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
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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Storage & Shelf Life
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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Shipping
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
MRPS24, a mitochondrial ribosomal protein, plays a crucial role in mitochondrial protein synthesis and is essential for proper cellular metabolism. Recent studies have highlighted its importance in various physiological processes, including energy production, apoptosis, and the regulation of mitochondrial dynamics. Dysregulation of MRPS24 has been linked to several diseases, including neurodegenerative disorders and certain cancers, where mitochondrial dysfunction is a contributing factor. Given the pivotal role of mitochondria in cell health and disease, understanding the structure and function of MRPS24 is fundamental. Researchers are increasingly focused on characterizing the MRPS24 protein to elucidate its specific interactions within the mitochondrial ribosome and its potential implications in mitochondrial biogenesis and function. Furthermore, exploring the effects of MRPS24 mutations or altered expression levels could reveal novel therapeutic targets for related disorders, making it an important area of investigation in mitochondrial biology and medical research. Overall, the study of MRPS24 is significant not only for fundamental science but also for its potential translational applications in understanding and treating mitochondrial diseases.
