Analytical Data
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Gene name
MRPS10
- Application
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Alternative Names
MRPS10; MSTP04028S ribosomal protein S10; mitochondrial; MRP-S10; S10mt; Mitochondrial small ribosomal subunit protein uS10m
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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
P82664
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Expression Region
1-201 aa
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AA Sequence
MAARTAFGAV CRRLWQGLGN FSVNTSKGNT AKNGGLLLST NMKWVQFSNL HVDVPKDLTK PVVTISDEPD ILYKRLSVLV KGHDKAVLDS YEYFAVLAAK ELGISIKVHE PPRKIERFTL LQSVHIYKKH RVQYEMRTLY RCLELEHLTG STADVYLEYI QRNLPEGVAM EVTKTQLEQL PEHIKEPIWE TLSEEKEESK S
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Molecular Weight
22.9 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
Related Products
Protein Description
MRPS10, or Mitochondrial Ribosomal Protein S10, plays a crucial role in mitochondrial function and protein synthesis. As a component of the mitochondrial ribosome, MRPS10 is involved in translating mitochondrial mRNA into functional proteins essential for oxidative phosphorylation and ATP production. Research has highlighted the importance of MRPS10 in maintaining mitochondrial integrity and cellular metabolism. Mutations or dysregulation of MRPS10 have been linked to various mitochondrial diseases and metabolic disorders, underscoring its significance in human health. Moreover, studies suggest that MRPS10 may have implications in neurodegenerative diseases and age-related conditions, as mitochondrial dysfunction is a common feature in these disorders. Given its central role in mitochondrial biology, investigating the function and regulation of MRPS10 offers insights into potential therapeutic strategies for mitochondrial diseases and could aid in understanding the broader implications of mitochondrial dysfunction in aging and disease.
