Anti-Moesin antibody [EPR2428(2)]

8 product images

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  Immunoprecipitation - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Immunoprecipitation of MSN in HeLa cells. Lysates were prepared and immunoprecipitation was performed using 1.0 μg of ab151542 pre-coupled to prot.A-Sepharose beads. Samples were washed and processed for western blot with Anti-Moesin antibody [EPR2429(2)] ab169789 at 1/10000. SM=10% starting material; UB=10% unbound fraction; IP=immunoprecipitate. These data were provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.

  All lanes: Immunoprecipitation - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Predicted band size: 68 kDa

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  Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Lane 1: Wild-type HAP1 whole cell lysate (20 μg)
  Lane 2: Moesin knockout HAP1 whole cell lysate (20 μg)
  Lane 3: HeLa whole cell lysate (20 μg)
  Lane 4: Raji whole cell lysate (20 μg)
  

  Lanes 1 - 4: Merged signal (red and green). Green - ab151542 observed at 75 kDa. Red - loading control, Anti-GAPDH antibody [mAbcam 9484] - Loading Control ab9484, observed at 37 kDa.

  ab151542 was shown to specifically react with Moesin in wild-type HAP1 cells as signal was lost in Moesin knockout cells. Wild-type and Moesin knockout samples were subjected to SDS-PAGE. ab151542 and Anti-GAPDH antibody [mAbcam 9484] - Loading Control ab9484 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Predicted band size: 68 kDa

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  Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  False colour image of Western blot: Anti-Moesin antibody [EPR2428(2)] staining at 2 μg/ml, shown in green; Mouse anti-GAPDH antibody [6C5] (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab151542 was shown to bind specifically to Moesin. A band was observed at 75 kDa in wild-type HeLa cell lysates with no signal observed at this size in MSN knockout cell line Human MSN (Moesin) knockout HeLa cell line ab265020 (knockout cell lysate Human MSN (Moesin) knockout HeLa cell lysate ab257542). To generate this image, wild-type and MSN knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween^® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) at 1/20000 dilution.

  All lanes: Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542) at 2 µg/mL

  Lane 1: Wild-type HeLa cell lysate at 20 µg

  Lane 2: MSN knockout HeLa cell lysate at 20 µg

  Lane 2: Western blot - Human MSN (Moesin) knockout HeLa cell line (Human MSN (Moesin) knockout HeLa cell line ab265020)

  Performed under reducing conditions.

  Predicted band size: 68 kDa

  Observed band size: 75 kDa

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  Immunocytochemistry/ Immunofluorescence - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  ab151542 was shown to react with MSN in wild-type HeLa cells in Immunocytochemistry with loss of signal observed in MSN knockout cell line Human MSN (Moesin) knockout HeLa cell line ab265020. Wild-type and knockout cells were mixed and pelleted at a 1:1 ratio on coverslips. The cells were fixed with 4% paraformaldehyde (15 min) then permeabilized with 0.1% Triton X-100 (10min) and then blocked with 1/10000. The cells were then incubated with ab151542 at 1/200 dilution overnight at 4°C followed by a further incubation at room temperature for 1h with a goat anti-rabbit secondary antibody to (Alexa Fluor^® 555) at 0.5 μg/ml. Acquisition of the green (wild-type), red (antibody staining) and far-red (knockout) channels was performed. Representative grayscale images of the red channel are shown. Wild-type and knockout cells are outlined with yellow and magenta dashed line, respectively. Schematic representation of the mosaic strategy used is shown on the bottom-right panel. Image was acquired with a Zeiss(LSM-880). These data were provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.

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  Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  All lanes: Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542) at 1/1000 dilution

  Lane 1: Raji cell lysate at 10 µg

  Lane 2: Jurkat cell lysate at 10 µg

  Lane 3: HeLa cell lysate at 10 µg

  Secondary

  All lanes: Goat anti-rabbit HRP at 1/2000 dilution

  Predicted band size: 68 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Immunohistochemical analysis of paraffin-embedded Human breast carcinoma tissue labeling Moesin with ab151542 at 1/100 dilution.
  

  Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.

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  Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  ab151542 was shown to react with MSN in wild-type HeLa cells in Western blot with loss of signal observed in MSN knockout cell line Human MSN (Moesin) knockout HeLa cell line ab265020 (MSN knockout cell lysate Human MSN (Moesin) knockout HeLa cell lysate ab257542). Wild-type HeLa and MSN knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 5% milk in TBST for 1 hr before incubation with ab151542 overnight at 4 °C at a 1/1000 dilution. Blots were incubated with goat anti-rabbit HRP secondary antibodies at 0.2ug/mL before imaging. These data were provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.

  All lanes: Western blot - Anti-Moesin antibody [EPR2428(2)] (ab151542) at 1/1000 dilution

  Lane 1: Wild-type HeLa cell lysate at 20 µg

  Lane 2: MSN knockout HeLa cell lysate at 20 µg

  Lane 2: Western blot - Human MSN (Moesin) knockout HeLa cell line (Human MSN (Moesin) knockout HeLa cell line ab265020)

  Performed under reducing conditions.

  Predicted band size: 68 kDa

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  Immunocytochemistry/ Immunofluorescence - Anti-Moesin antibody [EPR2428(2)] (ab151542)

  Immunofluorescent analysis of Raji cells labeling Moesin with ab151542 at 1/100 dilution.