GALE 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00002582-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

GALE transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: GALE transfected lysate ( 38.3 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-GALE full-length

    Host

    Human

    Theoretical MW (kDa)

    38.3

    Interspecies Antigen Sequence

    Rat (93)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-GALE antibody (H00002582-B01) by Western Blots.

    SDS-PAGE Gel

    GALE transfected lysate.

    Western Blot

    Lane 1: GALE transfected lysate ( 38.3 KDa)
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — GALE

    Entrez GeneID

    2582

    GeneBank Accession#

    NM_000403.3

    Protein Accession#

    -

    Gene Name

    GALE

    Gene Alias

    FLJ95174, FLJ97302, SDR1E1

    Gene Description

    UDP-galactose-4-epimerase

    Omim ID

    230350 606953

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). Multiple alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq

    Other Designations

    OTTHUMP00000002991|OTTHUMP00000044857|UDP galactose-4'-epimerase|galactose-4-epimerase, UDP-|galactowaldenase|short chain dehydrogenase/reductase family 1E, member 1

  • Interactome
  • Pathway
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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