PPP1CC KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: Insertion of the selection cassette in exon 1.
PP1C, PP1G_HUMAN, PP1gamma, PPP 1G, PPP1CC, Protein phosphatase 1, catalytic subunit, gamma isozyme, Protein phosphatase 1C catalytic subunit, Serine/threonine phosphatase 1 gamma, Serine/threonine-protein phosphatase PP1-gamma catalytic subunit
PPP1CC KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: Insertion of the selection cassette in exon 1.
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Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
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Lane 2: PPP1CC knockout HeLa cell lysate (20 μg)
Lane 3: T-47D cell lysate (20 μg)
Lane 4: 293T cell lysate (20 μg)
Lanes 1-4: Merged signal (red and green). Green - Anti-PP1C gamma antibody [EPR8934] ab134947 observed at 37 kDa. Red - loading control Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 observed at 50 kDa.
Anti-PP1C gamma antibody [EPR8934] ab134947 Anti-Protein phosphatase 1 gamma 2 antibody was shown to specifically react with Protein phosphatase 1 gamma 2 in wild-type HeLa cells. Loss of signal was observed when knockout cell line Human PPP1CC (PP1C gamma) knockout HeLa cell line ab264875 (knockout cell lysate ab258131) was used. Wild-type and Protein phosphatase 1 gamma 2 knockout samples were subjected to SDS-PAGE. Anti-PP1C gamma antibody [EPR8934] ab134947 and Anti-alpha Tubulin antibody [DM1A] - Loading Control (Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (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.
All lanes: Western blot - Anti-PP1C gamma antibody [EPR8934] (Anti-PP1C gamma antibody [EPR8934] ab134947) at 1/1000 dilution
Lane 1: Wild-type HeLa cell lysate at 20 µg
Lane 2: PPP1CC knockout HeLa cell lysate at 20 µg
Lane 2: Western blot - Human PPP1CC (PP1C gamma) knockout HeLa cell line (Human PPP1CC (PP1C gamma) knockout HeLa cell line ab264875)
Lane 3: T-47D cell lysate at 20 µg
Lane 4: 293T cell lysate at 20 µg
All lanes: Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) at 1/10000 dilution
Predicted band size: 27 kDa, 37 kDa, 42 kDa
Observed band size: 28 kDa, 37 kDa, 38 kDa
Homozygous: Insertion of the selection cassette in exon 1
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