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Recombinant Human 39S ribosomal protein L40, mitochondrial (MRPL40)

ACP10934

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP10934 Target NameMRPL40
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range47-206Protein LengthFull Length of Mature Protein
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ9NQ50
Background Information
  • Uniprot Id

    Q9NQ50

  • Target Species

    Human

  • Target Name

    MRPL40

  • Target Full Name

    Large ribosomal subunit protein mL40

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    Mitochondrion-specific ribosomal protein mL40 family

  • Target Tissue Specificity

    Ubiquitous.

  • Target Synonyms

    MRPL40; NLVCF; URIM; 39S ribosomal protein L40; mitochondrial; L40mt; MRP-L40; Mitochondrial large ribosomal subunit protein mL40; Nuclear localization signal-containing protein deleted in velocardiofacial syndrome; Up-regulated in metastasis

  • Target Background

    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 39S subunit protein. Deletions in this gene may contribute to the etiology of velo-cardio-facial syndrome and DiGeorge syndrome.

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