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Recombinant Protein of Human MRPS26, aa 1-205(Cat#: RIJL-0225-JL516)

This product is a recombinant human MRPS26 protein with N-terminal His Tag. It is availible for WB, bioactivity testing, immunogen, ELISA and SDS-PAGE.

Certificate of Analysis (COA)

To download the COA, please enter the product lot number in the following search box. For further assistance, you may also inquire via the following email address: [info@creative-biolabs.com].

Lot Number
Summary Related Products & Services

Description

This product is a recombinant human MRPS26 protein with N-terminal His Tag. It is availible for WB, bioactivity testing, immunogen, ELISA and SDS-PAGE.

Product Property

Species Reactivity Human
Molecule Mass 24 kDa
Purity >90% determined by SDS-PAGE
Endotoxin Low endotoxin
Expression Host E.coli
Formulation 25 mM Tris-HCl, pH 7.3, 100 mM glycine, 10% glycerol
Residues 1-205aa
Sequence MLRALSRLGAGTPCRPRAPLVLPARGRKTRHDPLAKSKIERVNMPPAVDPAEFFVLMERYQHYRQTVRALRMEFVSEVQRKVHEARAGVLAERKALKDAAEHRELMAWNQAENRRLHELRIARLRQEEREQEQRQALEQARKAEEVQAWAQRKEREVLQLQEEVKNFITRENLEARVEAALDSRKNYNWAITREGLVVRPQRRDS
Product Form Lyophilized powder
Tags N-terminal His Tag
Type Recombinant Protein
Applications WB; Bioactivity Testing; Immunogen; ELISA; SDS-PAGE
Storage Store at -20°C/-80°C. Avoid freeze-thaw cycles.

Target

Alternative Names MRPS26; C20orf193; GI008; MRP-S13; NY-BR-87; RPMS13; S13mt; S26mt; MRP-S26; MRPS13
Gene ID 64949
UniProt ID Q9BYN8
Location Mitochondrion
Introduction MRPS26 protein functions as a vital element within the small subunit of the mitochondrial ribosome, playing a crucial part in the biosynthesis of mitochondrial proteins. Genetic mutations or alterations affecting the MRPS26 gene have been associated with a variety of mitochondrial diseases, notably including Leigh syndrome, a profound neurodegenerative disorder, as well as other genetic conditions marked by impaired oxidative phosphorylation and subsequent cellular energy deficiencies.
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
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