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.
Summary
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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.