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Immunohistochemical staining of human vulva/anal skin shows strong nuclear and cytoplasmic positivity in squamous epithelial cells.
Immunohistochemical staining of human vulva/anal skin shows strong nuclear and cytoplasmic positivity in squamous epithelial cells.
Immunohistochemical staining of human vulva/anal skin shows strong nuclear and cytoplasmic positivity in squamous epithelial cells.

Anti-CRABP2 Antibody

HPA004135
Atlas Antibodies
ApplicationsWestern Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetCRABP2
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-CRABP2
  • Delivery Days Customer
    4
  • Applications
    Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID1382
  • Target name
    CRABP2
  • Target description
    cellular retinoic acid binding protein 2
  • Target synonyms
    CRABP-II, RBP6, cellular retinoic acid-binding protein 2, cellular retinoic acid-binding protein II
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP29373
  • Protein Name
    Cellular retinoic acid-binding 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 CRABP2 using anti-CRABP2 antibody (A03297-3). 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 MCF-7 whole cell lysates, Lane 2: human T-47D 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-CRABP2 antigen affinity purified polyclonal antibody (Catalog # A03297-3) 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 CRABP2 at approximately 17 kDa. The expected band size for CRABP2 is at 17 kDa.
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