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Immunology Innate Immunity Macrophage / Inflamm.

Human CAPG (MCP) knockout HeLa cell lysate (ab257378)

Price and availability

331 689 ₸

Availability

Order now and get it on Wednesday March 03, 2021

Human CAPG (MCP) knockout HeLa cell lysate (ab257378)
  • 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)
  • 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
    ab260976 - Human CAPG knockout HeLa cell lysate 1 x 100µg
    ab255929 - Human wild-type HeLa cell lysate 1 x 100µg
  • Research areas

    • Immunology
    • Innate Immunity
    • Macrophage / Inflamm.
    • Signal Transduction
    • Cytoskeleton / ECM
    • Cytoskeleton
    • Microfilaments
    • Actin etc
    • Actin
  • 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 CAPG knockout HeLa cell lysate (ab257378)
    Western blot - Human CAPG knockout HeLa cell lysate (ab257378)

    Lane 1:Wild-type HeLa cell lysate (20 ug)
    Lane 2:CAPG knockout HeLa cell lysate (20 ug)
    Lane 3:THP-1 cell lysate (20 ug)
    Lane 4:U-937 cell lysate (20 ug)

    ab181092 was shown to specifically react with Actin Regulatory Protein CAPG/MCP in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265766 (knockout cell lysate ab257378) was used. Wild-type and Actin Regulatory Protein CAPG/MCP knockout samples were subjected to SDS-PAGE. ab181092 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated at room temperature for 2.5 hours 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 CAPG knockout HeLa cell lysate (ab257378)
    Western blot - Human CAPG knockout HeLa cell lysate (ab257378)

    Lane 1:Wild-type HeLa cell lysate (20 ug)
    Lane 2:CAPG knockout HeLa cell lysate (20 ug)
    Lane 3:THP-1 cell lysate (20 ug)
    Lane 4:U-937 cell lysate (20 ug)

    ab181095 was shown to specifically react with Actin Regulatory Protein CAPG/MCP in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265766 (knockout cell lysate ab257378) was used. Wild-type and Actin Regulatory Protein CAPG/MCP knockout samples were subjected to SDS-PAGE. ab181095 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated at room temperature for 2.5 hours 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.

  • Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)
    Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)

    Allele-1: 2 bp deletion in exon 2

     

  • Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)
    Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)

    Allele-2: 1 bp insertion in exon 2

     

  • Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)
    Sanger Sequencing - Human CAPG knockout HeLa cell lysate (ab257378)

    Allele-3: Insertion of the selection cassette in exon 2

     

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