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Immunohistochemical staining of human skeletal muscle shows moderate nuclear positivity in myocytes.
Immunohistochemical staining of human skeletal muscle shows moderate nuclear positivity in myocytes.
Immunohistochemical staining of human skeletal muscle shows moderate nuclear positivity in myocytes.

Anti-NFIC Antibody

HPA052625
Atlas Antibodies
ApplicationsChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetNFIC
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-NFIC
  • Delivery Days Customer
    4
  • Applications
    ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID4782
  • Target name
    NFIC
  • Target description
    nuclear factor I C
  • Target synonyms
    CCAAT-box-binding transcription factor; CTF; CTF5; NF1-C; NFI; NF-I; NF-I/C; nuclear factor 1 C-type; nuclear factor I/C (CCAAT-binding transcription factor); TGGCA-binding protein
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP08651
  • Protein Name
    Nuclear factor 1 C-type
  • 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 NFIC using anti-NFIC antibody (A04154-2). 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 50ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human T-47D whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human A431 whole cell lysates, Lane 7: human Caco-2 whole cell lysates, Lane 8: rat skeletal muscle tissue lysates, Lane 9: mouse RAW264.7 whole cell lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-NFIC antigen affinity purified polyclonal antibody (Catalog # A04154-2) 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. Specific bands were detected for NFIC at approximately 55-65, 70KD. The expected band size for NFIC is at 56KD.
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