Analytical Data
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Gene name
MRPS7
- Application
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Alternative Names
28S ribosomal protein S7; 28S ribosomal protein S7. mitochondrial precursor; 30S ribosomal protein S7 homolog; bMRP 27a; bMRP-27a; bMRP27a; mitochondrial; Mitochondrial ribosomal protein S7; MRP S; MRP S7; MRP-S7; MRPS; mrps7; RP S7; RPMS7; RPS7; RT07_HUMAN; S7mt
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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
Q9Y2R9
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Expression Region
38-242 aa
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AA Sequence
SPE FKDPLIDKEY YRKPVEELTE EEKYVRELKK TQLIKAAPAG KTSSVFEDPV ISKFTNMMMI GGNKVLARSL MIQTLEAVKR KQFEKYHAAS AEEQATIERN PYTIFHQALK NCEPMIGLVP ILKGGRFYQV PVPLPDRRRR FLAMKWMITE CRDKKHQRTL MPEKLSHKLL EAFHNQGPVI KRKHDLHKMA EANRALAHYR WW
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Molecular Weight
28.1 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
MRPS7 (mitochondrial ribosomal protein S7) is a pivotal protein encoded by the nuclear genome, playing a crucial role in mitochondrial protein synthesis and ribosome assembly. Research has increasingly focused on MRPS7 due to its potential implications in various diseases, including cancer and neurodegenerative disorders. Mitochondria are essential for energy production, and their dysfunction is linked to numerous pathologies. MRPS7 is integral to the proper functioning of mitochondrial ribosomes, influencing mitochondrial translation efficiency and the synthesis of vital proteins necessary for cellular respiration. Abnormalities in MRPS7 expression or function may contribute to impaired mitochondrial function, leading to metabolic disorders and other health issues. Given its critical role, detailed studies on MRPS7 can provide insights into mitochondrial physiology and pathology, paving the way for novel therapeutic strategies targeting mitochondrial dysfunctions. Researchers are increasingly utilizing recombinant MRPS7 proteins to understand its structure, function, and interaction with other mitochondrial components, which may illuminate mechanisms underlying mitochondrial diseases and offer potential avenues for drug development.
