ABAT 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00000018-T02

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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

ABAT transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: ABAT transfected lysate ( 56.40 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-ABAT full-length

    Host

    Human

    Theoretical MW (kDa)

    56.4

    Interspecies Antigen Sequence

    Mouse (91); Rat (92)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-ABAT antibody (H00000018-D01P) by Western Blots.

    SDS-PAGE Gel

    ABAT transfected lysate.

    Western Blot

    Lane 1: ABAT transfected lysate ( 56.40 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 — ABAT

    Entrez GeneID

    18

    GeneBank Accession#

    NM_000663.3

    Protein Accession#

    NP_000654.2

    Gene Name

    ABAT

    Gene Alias

    FLJ17813, GABA-AT, GABAT, NPD009

    Gene Description

    4-aminobutyrate aminotransferase

    Omim ID

    137150

    Gene Ontology

    Hyperlink

    Gene Summary

    4-aminobutyrate aminotransferase (ABAT) is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. The active enzyme is a homodimer of 50-kD subunits complexed to pyridoxal-5-phosphate. The protein sequence is over 95% similar to the pig protein. GABA is estimated to be present in nearly one-third of human synapses. ABAT in liver and brain is controlled by 2 codominant alleles with a frequency in a Caucasian population of 0.56 and 0.44. The ABAT deficiency phenotype includes psychomotor retardation, hypotonia, hyperreflexia, lethargy, refractory seizures, and EEG abnormalities. Multiple alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq

    Other Designations

    GABA aminotransferase|GABA transferase|gamma-amino-N-butyrate transaminase

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