TDP1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00055775-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

TDP1 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: TDP1 transfected lysate ( 68.4 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-TDP1 full-length

    Host

    Human

    Theoretical MW (kDa)

    66.99

    Interspecies Antigen Sequence

    Mouse (81); Rat (82)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-TDP1 antibody (H00055775-B01) by Western Blots.

    SDS-PAGE Gel

    TDP1 transfected lysate.

    Western Blot

    Lane 1: TDP1 transfected lysate ( 68.4 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 — TDP1

    Entrez GeneID

    55775

    GeneBank Accession#

    NM_001008744

    Protein Accession#

    NP_001008744

    Gene Name

    TDP1

    Gene Alias

    FLJ11090, MGC104252

    Gene Description

    tyrosyl-DNA phosphodiesterase 1

    Omim ID

    607198 607250

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. This protein may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains. Mutations in this gene are associated with the disease spinocerebellar ataxia with axonal neuropathy (SCAN1). While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform. [provided by RefSeq

    Other Designations

    -

  • Interactome
  • 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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