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Cardiovascular Blood Serum Proteins

Human B2M (beta 2 Microglobulin) knockout Hep G2 cell lysate (ab256846)

Human B2M (beta 2 Microglobulin) knockout Hep G2 cell lysate (ab256846)
  • 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)
  • 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
    ab263509 - Human B2M knockout HepG2 cell lysate 1 x 100µg
    ab263911 - Human wild-type HepG2 cell lysate 1 x 100µg
  • Research areas

    • Cardiovascular
    • Blood
    • Serum Proteins
    • Cancer
    • Tumor biomarkers
    • Globulins
    • Cardiovascular
    • Blood
    • Blood Cell Antigens
    • WBC Antigens
    • HLA
  • Cell type

    epithelial
  • Disease

    Hepatocellular Carcinoma

Images

  • Western blot - Human B2M (beta 2 Microglobulin) knockout HEPG2 cell lysate (ab256846)
    Western blot - Human B2M (beta 2 Microglobulin) knockout HEPG2 cell lysate (ab256846)

    Lane 1: Wild-type HepG2 cell lysate (20 ug)
    Lane 2: B2M knockout HepG2 cell lysate (20 ug)
    Lane 3: HeLa cell lysate (20 ug)
    Lane 4: Jurkat cell lysate (20 ug)

    ab75853 was shown to specifically react with beta 2 Microglobulin in wild-type HepG2 cells. Loss of signal was observed when knockout cell line ab262325 (knockout cell lysate ab256846) was used. Wild-type and beta 2 Microglobulin knockout samples were subjected to SDS-PAGE. ab75853 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4oC at 1 in 1000 dilution 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 B2M (beta 2 Microglobulin) knockout HEPG2 cell lysate (ab256846)
    Western blot - Human B2M (beta 2 Microglobulin) knockout HEPG2 cell lysate (ab256846)

    Lane 1: Wild-type HepG2 cell lysate (20 ug)
    Lane 2: B2M knockout HepG2 cell lysate (20 ug)
    Lane 3: HeLa cell lysate (20 ug)
    Lane 4: Jurkat cell lysate (20 ug)

    ab218230 was shown to specifically react with beta 2 Microglobulin in wild-type HepG2 cells. Loss of signal was observed when knockout cell line ab262325 (knockout cell lysate ab256846) was used. Wild-type and beta 2 Microglobulin knockout samples were subjected to SDS-PAGE. ab218230 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4oC at 1 in 500 dilution 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 B2M knockout HEPG2 cell lysate (ab256846)
    Sanger Sequencing - Human B2M knockout HEPG2 cell lysate (ab256846)

    Allele-1: 1 bp insertion in exon1

     

  • Sanger Sequencing - Human B2M knockout HEPG2 cell lysate (ab256846)
    Sanger Sequencing - Human B2M knockout HEPG2 cell lysate (ab256846)

    Allele-2: Insertion of the selection cassette in exon1

     

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