Recombinant Human GALT protein (ab139613)

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Description

  • Product name

    Recombinant Human GALT protein

  • Purity

    > 85 % SDS-PAGE.
    ab139613 is purified using conventional chromatography techniques.

  • Expression system

    Escherichia coli

  • Accession

    P07902

  • Protein length

    Full length protein

  • Animal free

    No

  • Nature

    Recombinant

    • Species

      Human

    • Sequence

      MGSSHHHHHH SSGLVPRGSH MGSHMSRSGT DPQQRQQASE ADAAAATFRA NDHQHIRYNP LQDEWVLVSA HRMKRPWQGQ VEPQLLKTVP RHDPLNPLCP GAIRANGEVN PQYDSTFLFD NDFPALQPDA PSPGPSDHPL FQAKSARGVC KVMCFHPWSD VTLPLMSVPE IRAVVDAWAS VTEELGAQYP WVQIFENKGA MMGCSNPHPH CQVWASSFLP DIAQREERSQ QAYKSQHGEP LLMEYSRQEL LRKERLVLTS EHWLVLVPFW ATWPYQTLLL PRRHVRRLPE LTPAERDDLA SIMKKLLTKY DNLFETSFPY SMGWHGAPTG SEAGANWNHW QLHAHYYPPL LRSATVRKFM VGYEMLAQAQ RDLTPEQAAE RLRALPEVHY HLGQKDRETA TIA

    • Predicted molecular weight

      46 kDa including tags

    • Amino acids

      1 to 379

    • Tags

      His tag N-Terminus

Specifications

Our Abpromise guarantee covers the use of ab139613 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

  • Form

    Liquid
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

    pH: 8.50
    Constituents: 0.32% Tris HCl, 10% Glycerol, 1.17% Sodium chloride

General Info

  • Alternative names

    • Gal 1 P uridylyltransferase
    • Gal-1-P uridylyltransferase
    • Galactose 1 phosphate uridyl transferase
    • Galactose 1 phosphate uridylyltransferase
    • Galactose-1-phosphate uridylyltransferase
    • GALT
    • GALT_HUMAN
    • UDP glucose hexose 1 phosphate uridylyltransferase
    • UDP-glucose--hexose-1-phosphate uridylyltransferase
    see all

  • Pathway

    Carbohydrate metabolism; galactose metabolism.

  • Involvement in disease

    Defects in GALT are the cause of galactosemia (GALCT) [MIM:230400]. Galactosemia is an inherited disorder of galactose metabolism that causes jaundice, cataracts, and mental retardation.

  • Sequence similarities

    Belongs to the galactose-1-phosphate uridylyltransferase type 1 family.
  • Information by UniProt

Images

  • SDS-PAGE - Recombinant Human GALT protein (ab139613)
    SDS-PAGE - Recombinant Human GALT protein (ab139613)
    15% SDS-PAGE analysis of ab139613 (3µg).

References

ab139613 has not yet been referenced specifically in any publications.

Publishing research using ab139613? Please let us know so that we can cite the reference in this datasheet.

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