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Western blot analysis in human cell lines Caco-2 and SK-MEL-30 using Anti-C1orf106 antibody. Corresponding C1orf106 RNA-seq data are presented for the same cell lines. Loading control: Anti-HDAC1.
Western blot analysis in human cell lines Caco-2 and SK-MEL-30 using Anti-C1orf106 antibody. Corresponding C1orf106 RNA-seq data are presented for the same cell lines. Loading control: Anti-HDAC1.
Western blot analysis in human cell lines Caco-2 and SK-MEL-30 using Anti-C1orf106 antibody. Corresponding C1orf106 RNA-seq data are presented for the same cell lines. Loading control: Anti-HDAC1.

Anti-C1orf106 Antibody

HPA027499
Atlas Antibodies
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetINAVA
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-C1orf106 Antibody
  • Delivery Days Customer
    4
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID55765
  • Target name
    INAVA
  • Target description
    innate immunity activator
  • Target synonyms
    C1orf106, innate immunity activator protein, uncharacterized protein C1orf106
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ3KP66
  • Protein Name
    Innate immunity activator protein
  • 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 INAVA using anti-INAVA antibody (A32411). 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 Hacat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: 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-INAVA antigen affinity purified polyclonal antibody (Catalog # A32411) 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 INAVA at approximately 70 kDa. The expected band size for INAVA is at 73 kDa.
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