You have changed your country from  to  . Please be aware that this will change the currency in the purchasing process.

Overview

  • Product nameGALE proteinSee all GALE proteins and peptides ...
  • Protein descriptionRecombinant full length Human GALE (amino acids 1-348) with N terminal His tag; 368 amino acids, MWt 40.4kDa (UniProt Q14376).
  • Uniprot accessionQ14376
  • Molecular weight40.400kDa inclusive of tags
  • Protein length348 amino acids
  • Expression hostE. coli
  • Properties

  • Purity> 95 % by SDS-PAGE
  • Purification notesab96767 is purified using conventional chromatography techniques.
  • E.C. Number5.1.3.2
  • FormLiquid
  • Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
  • Storage bufferPreservative: None
    Constituents: 10% Glycerol, 0.1M Sodium chloride, 5mM DTT, 20mM Tris HCl, 1mM EDTA, pH 8.0
  • Concentration information loading...
  • SequenceMGSSHHHHHHSSGLVPRGSHMAEKVLVTGGAGYIGSHTVL ELLEAGYLPVVIDNFHNAFRGGGSLPESLRRVQELTGRSV EFEEMDILDQGALQRLFKKYSFMAVIHFAGLKAVGESVQK PLDYYRVNLTGTIQLLEIMKAHGVKNLVFSSSATVYGNPQ YLPLDEAHPTGGCTNPYGKSKFFIEEMIRDLCQADKTWNA VLLRYFNPTGAHASGCIGEDPQGIPNNLMPYVSQVAIGRR EALNVFGNDYDTEDGTGVRDYIHVVDLAKGHIAALRKLKE QCGCRIYNLGTGTGYSVLQMVQAMEKASGKKIPYKVVARR EGDVAACYANPSLAQEELGWTAALGLDRMCEDLWRWQKQN PSGFGTQA
  • Research Areas
  • Applications

    Our Abpromise guarantee covers the use of ab96767 in the following tested applications.

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

    Application Notes
    MS MS: Use at an assay dependent dilution.
    SDS-PAGE SDS-PAGE: Use at an assay dependent dilution.
  • Application notesThis peptide can be used with studies using ab153824,ab155277 and ab155997.
  • Protein info

    • Alternative names
        FLJ95174FLJ97302Galactose 4 epimerase UDP
        GalactowaldenasegalEGALE_HUMANOTTHUMP00000002991OTTHUMP00000002994OTTHUMP00000037931OTTHUMP00000044857SDR1E1short chain dehydrogenase/reductase family 1E member 1UDP galactose 4 epimeraseUDP galactose 4' epimeraseUDP glucose 4 epimeraseUDP-galactose 4-epimeraseUDP-glucose 4-epimerase
      see all
  • FunctionCatalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine.
  • PathwayCarbohydrate metabolism; galactose metabolism.
  • Involvement in diseaseDefects in GALE are the cause of epimerase-deficiency galactosemia (EDG) [MIM:230350]; also known as galactosemia type 3. Clinical features include early-onset cataracts, liver damage, deafness and mental retardation. There are two clinically distinct forms of EDG. (1) A benign, or 'peripheral' form with no detectable GALE activity in red blood cells and characterized by mild symptoms. Some patients may suffer no symptoms beyond raised levels of galactose-1-phosphate in the blood. (2) A much rarer 'generalized' form with undetectable levels of GALE activity in all tissues and resulting in severe features such as restricted growth and mental development.
  • Sequence similaritiesBelongs to the sugar epimerase family.
  • Target information above from: UniProt accession Q14376 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt

    GALE protein images

    • 15% SDS-PAGE showing ab96767 at approximately 40.4kDa (3µg).

    References for GALE protein (ab96767)

    ab96767 has not yet been referenced specifically in any publications.

    Product Wall

    There are currently no Abreviews or Questions for ab96767.
    Please use the links above to contact us or submit feedback about this product.

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