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ICC/IF analysis of HeLa cells using GTX22043 MADD antibody. Dilution : 20 microg/ml
ICC/IF analysis of HeLa cells using GTX22043 MADD antibody. Dilution : 20 microg/ml
ICC/IF analysis of HeLa cells using GTX22043 MADD antibody. Dilution : 20 microg/ml

MADD antibody

GTX22043
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
Product group Antibodies
TargetMADD
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Overview

  • Supplier
    GeneTex
  • Product Name
    MADD antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:250-1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID8567
  • Target name
    MADD
  • Target description
    MAP kinase activating death domain
  • Target synonyms
    DEEAH; DENN; differentially expressed in normal and neoplastic cells; IG20; insulinoma glucagonoma clone 20; MAP kinase-activating death domain protein; NEDDISH; Rab3 GDP/GTP exchange factor; rab3 GDP/GTP exchange protein; RAB3GEP; RabGEF
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ8WXG6
  • Protein Name
    MAP kinase-activating death domain protein
  • Scientific Description
    Tumor necrosis factor alpha (TNF-alpha) is a signaling molecule that interacts with one of two receptors on cells targeted for apoptosis. The apoptotic signal is transduced inside these cells by cytoplasmic adaptor proteins. The protein encoded by this gene is a death domain-containing adaptor protein that interacts with the death domain of TNF-alpha receptor 1 to activate mitogen-activated protein kinase (MAPK) and propagate the apoptotic signal. It is membrane-bound and expressed at a higher level in neoplastic cells than in normal cells. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of MADD using anti-MADD antibody (A02030-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MADD antigen affinity purified polyclonal antibody (Catalog # A02030-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MADD at approximately 240 kDa. The expected band size for MADD is at 183 kDa.
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