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Immunohistochemical staining of human colon shows strong nuclear membrane positivity in glandular cells.
Immunohistochemical staining of human colon shows strong nuclear membrane positivity in glandular cells.
Immunohistochemical staining of human colon shows strong nuclear membrane positivity in glandular cells.

Anti-ING2 Antibody

HPA021517
Atlas Antibodies
ApplicationsWestern Blot, ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetING2
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-ING2 Antibody
  • Delivery Days Customer
    4
  • Applications
    Western Blot, ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID3622
  • Target name
    ING2
  • Target description
    inhibitor of growth family member 2
  • Target synonyms
    ING1L, p33ING2, inhibitor of growth protein 2, ING1Lp, inhibitor of growth 1-like protein, p32
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9H160
  • Protein Name
    Inhibitor of growth protein 2
  • Scientific Description
    Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
  • Reactivity
    Human
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116161

Datasheet

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MSDS

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Figure 1. Western blot analysis of ING2 using anti-ING2 antibody (A04290-3). 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 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat thymus tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse EL-4 whole cell lysates, Lane 8: mouse Ana-1 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-ING2 antigen affinity purified polyclonal antibody (Catalog # A04290-3) 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 ING2 at approximately 37 kDa. The expected band size for ING2 is at 33 kDa.
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