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Immunohistochemical staining of human cerebral cortex shows strong cytoplasmic positivity in neuronal cells, glial cells and neuropil.
Immunohistochemical staining of human cerebral cortex shows strong cytoplasmic positivity in neuronal cells, glial cells and neuropil.
Immunohistochemical staining of human cerebral cortex shows strong cytoplasmic positivity in neuronal cells, glial cells and neuropil.

Anti-MOAP1 Antibody

HPA076948
Atlas Antibodies
ApplicationsImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetMOAP1
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-MOAP1
  • Delivery Days Customer
    4
  • Applications
    ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID64112
  • Target name
    MOAP1
  • Target description
    modulator of apoptosis 1
  • Target synonyms
    MAP1; MAP-1; modulator of apoptosis 1; paraneoplastic antigen like 4; paraneoplastic antigen Ma4; paraneoplastic Ma antigen family member 4; PNMA4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ96BY2
  • Protein Name
    Modulator of apoptosis 1
  • Scientific Description
    Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
  • Reactivity
    Human
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116161

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Figure 1. Western blot analysis of MOAP1 using anti-MOAP1 antibody (A08043-1). 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 RT4 whole cell 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-MOAP1 antigen affinity purified polyclonal antibody (Catalog # A08043-1) 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 MOAP1 at approximately 35 kDa. The expected band size for MOAP1 is at 40 kDa.
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