Recombinant Human FLJ36733 protein (ab176034)

Overview

  • Product name
    Recombinant Human FLJ36733 protein
  • Protein length
    Protein fragment

Description

  • Nature
    Recombinant
  • Source
    Escherichia coli
  • Amino Acid Sequence
    • Accession
    • Species
      Human
    • Sequence
      MGSSHHHHHH SSGLVPRGSH MGSNKWSKVR HIKGPKDVER SRIFSKLCLN IRLAVKEGGP NPEHNSNLAN ILEVCRSKHM PKSTIETALK MEKSKDTYLL YEGRGPGGSS LLIEALSNSS HKCQADIRHI LNKNGGVMAV GARHSFDKKG VIVVEVEDRE KKAVNLERAL EMAIEAGAED VKETEDEEER NVFKFICDAS SLHQVRKKLD SLGLCSVSCA LEFIPNSKVQ LAEPDLEQAA HLIQALSNHE DVIHVYDNIE
    • Molecular weight
      29 kDa including tags
    • Amino acids
      61 to 297
    • Tags
      His tag N-Terminus
    • Additional sequence information
      (NP_057444).

Specifications

Our Abpromise guarantee covers the use of ab176034 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    SDS-PAGE

    Mass Spectrometry

  • Mass spectrometry
    MALDI-TOF
  • Purity
    >95% by SDS-PAGE .
    Purified using conventional chromatography techniques.
  • Form
    Liquid
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

    Information available upon request.

General Info

  • Alternative names
    • CCDC44
    • CDNA FLJ36733 fis
    • Coiled coil domain containing 44
    • Coiled-coil domain-containing protein 44
    • PRO0477
    • Taco1
    • TACO1_HUMAN
    • Translational activator of cytochrome c oxidase 1
    • Translational activator of mitochondrially-encoded cytochrome c oxidase I
    • UTERU2012856
    see all
  • Function
    Acts as a translational activator of mitochondrially-encoded cytochrome c oxidase 1.
  • Involvement in disease
    Defects in TACO1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions that is commonly associated with systemic cytochrome c oxidase (COX) deficiency.
  • Sequence similarities
    Belongs to the TACO1 family.
  • Cellular localization
    Mitochondrion.
  • Information by UniProt

Images

  • 15% SDS-PAGE analysis of ab176034 (3µg).

References

ab176034 has not yet been referenced specifically in any publications.

Customer reviews and Q&As

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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