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Western blot analysis of extracts from K562 cells, using MRPS12 antibody.
Western blot analysis of extracts from K562 cells, using MRPS12 antibody.
Western blot analysis of extracts from K562 cells, using MRPS12 antibody.

MRPS12 Antibody

CSB-PA788592
Cusabio
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetMRPS12
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Overview

  • Supplier
    Cusabio
  • Product Name
    MRPS12 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID6183
  • Target name
    MRPS12
  • Target description
    mitochondrial ribosomal protein S12
  • Target synonyms
    28S ribosomal protein S12, mitochondrial; mitochondrial small ribosomal subunit protein uS12m; MPR-S12; MRP-S12; MT-RPS12; RPMS12; RPS12; RPSM12; S12mt
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO15235
  • Protein Name
    28S ribosomal protein S12, mitochondrial
  • Scientific Description
    Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S12P family. The encoded protein is a key component of the ribosomal small subunit and controls the decoding fidelity and susceptibility to aminoglycoside antibiotics. The gene for mitochondrial seryl-tRNA synthetase is located upstream and adjacent to this gene, and both genes are possible candidates for the autosomal dominant deafness gene (DFNA4). Splice variants that differ in the 5 UTR have been found for this gene; all three variants encode the same protein. Shah Z.H., Gene 204:55-62(1997). Johnson D.F., Genomics 52:363-368(1998). Ebert L., Submitted (MAY-2004) to the EMBL/GenBank/DDBJ databases.
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    12352203