Analytical Data
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Gene name
MRPL28
- Application
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Alternative Names
Melanoma antigen p15 Melanoma-associated antigen recognized by T-lymphocytes
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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
Q13084
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Expression Region
1-256aa
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Molecular Weight
57.2 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
MRPL28, a mitochondrial ribosomal protein, plays a crucial role in the biogenesis of mitochondrial ribosomes and the regulation of mitochondrial protein synthesis. Dysregulation of mitochondrial protein synthesis is linked to various human diseases, including mitochondrial disorders, neurodegenerative diseases, and certain types of cancer. Research into MRPL28 has gained momentum as scientists aim to understand its function within the mitochondrial ribosome and its implications for mitochondrial health. Notably, recent studies suggest that alterations in MRPL28 expression and function may impact cellular metabolism and stress responses, underscoring its potential role in disease development. Moreover, MRPL28 is believed to interact with other mitochondrial ribosomal proteins and factors, indicating its importance in maintaining the integrity and functionality of mitochondrial translation machinery. Investigating MRPL28 not only enhances our understanding of mitochondrial biology but also opens avenues for therapeutic strategies aimed at correcting mitochondrial dysfunctions. Given the growing body of evidence linking mitochondrial dysfunction to a range of pathologies, continued research on MRPL28 presents a promising frontier in the field of molecular and cellular biology.
