Analytical Data
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Gene name
MRPL55
- Application
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Alternative Names
39S ribosomal protein L55; 39S ribosomal protein L55; mitochondrial; AAVG5835; DKFZp686D1387; L55mt; L55nt; MGC61802; mitochondrial; Mitochondrial ribosomal protein L55; MRP L55; MRP-L55; MRPL55; PRO19675; RM55_HUMAN
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Species
Human
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Source
E. coli
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Tag
N- GST
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q7Z7F7
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Expression Region
34-128aa
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Molecular Weight
38.6 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
MRPL55, a mitochondrial ribosomal protein, plays a crucial role in the biogenesis of mitochondrial ribosomes and protein synthesis within mitochondria. Mitochondria are essential organelles responsible for energy production and metabolic regulation, and their dysfunction is linked to various diseases, including neurodegenerative disorders and metabolic syndromes. The study of MRPL55 has gained attention due to its involvement in the mitochondrial translation process, which is vital for encoding mitochondrial DNA-encoded proteins essential for oxidative phosphorylation. Research has indicated that altered expression or mutations in MRPL55 can lead to mitochondrial dysfunction, highlighting its importance in cellular energy homeostasis. Furthermore, understanding the molecular mechanisms by which MRPL55 operates may reveal insights into the pathophysiology of mitochondrial diseases and offer potential therapeutic targets. The investigation of MRPL55's structure, function, and interaction with other mitochondrial components is essential for elucidating its role in health and disease. As research progresses, MRPL55 could emerge as a key player in developing mitochondrial-targeted therapies, underscoring the significance of detailing its functional attributes and regulatory mechanisms in both normal physiology and pathological conditions.
