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Brand: ProteoGenix

Recombinant Human MRPS17 Protein, N-His

Host species:
Escherichia coli (E.coli)
Origin species:
Human
Molecular weight:
16.67 kDa

$392.00

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Met1–Gln130
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Recombinant Human MRPS17 Protein, N-His

Recombinant Human MRPS17 Protein, N-His

Product name Recombinant Human MRPS17 Protein, N-His
Origin species Human
Expression system Prokaryotic expression
Molecular weight 16.67 kDa
Buffer Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Delivery condition Dry Ice
Delivery lead time in business days 3-5 days if in stock; 3-5 weeks if production needed
Storage condition 4°C for short term (1 week), -20°C or -80°C for long term (avoid freezing/thawing cycles; addition of 20-40% glycerol improves cryoprotection)
Brand ProteoGenix
Host species Escherichia coli (E.coli)
Fragment Type Met1-Gln130
Aliases /Synonyms MRP-S17, MRPS17, S17mt, 28S ribosomal protein S17, mitochondrial, RPMS17, Mitochondrial small ribosomal subunit protein uS17m
Reference ARO-P12281
Note For research use only.
Molecular Constructor
Met1–Gln130

Title: Introduction to Recombinant Human MRPS17 Protein

Recombinant Human MRPS17 Protein, also known as Mitochondrial Ribosomal Protein S17, is a highly conserved protein that plays a crucial role in the assembly and function of the mitochondrial ribosome. This protein is encoded by the MRPS17 gene and is found in both prokaryotic and eukaryotic cells. In this article, we will explore the structure, activity, and application of Recombinant Human MRPS17 Protein.

Structure of Recombinant Human MRPS17 Protein

Recombinant Human MRPS17 Protein is a 15 kDa protein consisting of 140 amino acids. It contains a single S17 domain, which is responsible for its binding to the 16S ribosomal RNA in the small subunit of the mitochondrial ribosome. The crystal structure of MRPS17 has been determined, revealing a conserved beta-barrel fold with a central helix. This structure is essential for its function in ribosome assembly and protein synthesis.

Activity of Recombinant Human MRPS17 Protein

Recombinant Human MRPS17 Protein plays a crucial role in the assembly and function of the mitochondrial ribosome. It is involved in the early stages of ribosome assembly, where it binds to the 16S rRNA and helps in the folding and stabilization of the small ribosomal subunit. MRPS17 also interacts with other ribosomal proteins and is essential for the proper functioning of the ribosome.

Furthermore, Recombinant Human MRPS17 Protein is involved in the translation process, where it helps in the recognition of the start codon and the initiation of protein synthesis. It also plays a role in the maintenance and stability of the mitochondrial genome, as mutations in the MRPS17 gene have been linked to mitochondrial disorders.

Application of Recombinant Human MRPS17 Protein

Recombinant Human MRPS17 Protein has a wide range of applications in both research and industrial settings. In the research field, this protein is used to study the structure and function of the mitochondrial ribosome and its role in protein synthesis. It is also used to investigate the effects of MRPS17 mutations on mitochondrial disorders and to develop potential treatments for these disorders.

In the industrial sector, Recombinant Human MRPS17 Protein is used in the production of recombinant proteins. As it is involved in the translation process, it can be used to optimize the expression of heterologous proteins in various expression systems. This protein can also be used as an antigen in the development of diagnostic assays for mitochondrial disorders.

Conclusion

In conclusion, Recombinant Human MRPS17 Protein is a highly conserved protein that plays a crucial role in the assembly and function of the mitochondrial ribosome. Its structure, activity, and application make it a valuable tool in the study of mitochondrial disorders and the production of recombinant proteins. Further research on this protein may lead to a better understanding of its role in protein synthesis and potential therapeutic interventions for mitochondrial disorders.

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