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Signal Transduction Growth Factors/Hormones Insulin / Insulin-like

Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)

Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

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Properties

  • Storage instructions

    Store at -80°C. Please refer to protocols.
  • Components 1 kit
    ab260084 - Human IGF1R knockout HeLa cell lysate 1 x 100µg
    ab255552 - Human wild-type HeLa cell lysate 1 x 100µg
  • Research areas

    • Signal Transduction
    • Growth Factors/Hormones
    • Insulin / Insulin-like
    • Cancer
    • Growth factors
    • Insulin and insulin-like
    • Developmental Biology
    • Post embryonic development
    • Aging
  • Cell type

    epithelial
  • Disease

    Adenocarcinoma
  • Gender

    Female
  • STR Analysis

    Amelogenin X D5S818: 11, 12 D13S317: 12, 13.3 D7S820: 8, 12 D16S539: 9, 10 vWA: 16, 18 TH01: 7 TPOX: 8, 12 CSF1PO: 9, 10

Images

  • Western blot - Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)
    Western blot - Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)
    Lane 1: Wild-type HeLa cell lysate (20µg)

    Lane 2: IGF1R knockout HeLa cell lysate (20µg)
    Lanes 1- 2: Merged signal (red and green). Green - ab263907 observed at 100 kDa. Red - loading control ab8245 observed at 37 kDa.
    ab263907 Anti-IGF1 Receptor antibody [EPR23027-80] was shown to specifically react with IGF1 Receptor in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab264801 (knockout cell lysate ab256951) was used. Wild-type and IGF1 Receptor knockout samples were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab263907 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
  • Western blot - Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)
    Western blot - Human IGF1R (IGF1 Receptor) knockout HeLa cell lysate (ab256951)
    Lane 1: Wild-type HeLa cell lysate (20µg)

    Lane 2: IGF1R knockout HeLa cell lysate (20µg)
    Lanes 1- 2: Merged signal (red and green). Green - ab182408 observed at 100 kDa. Red - loading control ab8245 observed at 37 kDa.
    ab182408 Anti-IGF1 Receptor antibody [EPR19322] was shown to specifically react with IGF1 Receptor in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab264801 (knockout cell lysate ab256951) was used. Wild-type and IGF1 Receptor knockout samples were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab182408 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
  • Sanger Sequencing - Human IGF1R knockout HeLa cell lysate (ab256951)
    Sanger Sequencing - Human IGF1R knockout HeLa cell lysate (ab256951)

    Allele-1: 13 bp deletion in exon 2; Allele-2: 1 bp deletion in exon 2

     

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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