Anti-GPNMB antibody [EPR22011-47] - BSA and Azide free

4 product images

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  Immunocytochemistry/ Immunofluorescence - Anti-GPNMB antibody [EPR22011-47] - BSA and Azide free (ab236211)

  Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized SK-MEL-28 (human malignant melanoma) and HeLa (human epithelial cell line from cervix adenocarcinoma) cells labeling GPNMB with Anti-GPNMB antibody [EPR22011-47] ab235873 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/1000 dilution (green).
  

  Confocal image showing cytoplasmic staining in SK-MEL-28 cell line.

  Negative control: HeLa （PMID: 20056711.

  The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594) (Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889) (red) at 1/200 dilution.

  Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/1000 dilution.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-GPNMB antibody [EPR22011-47] ab235873).

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  Flow Cytometry (Intracellular) - Anti-GPNMB antibody [EPR22011-47] - BSA and Azide free (ab236211)

  Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell, Left panel) and SK-MEL-28 (human malignant melanoma, Right panel) labeling GPNMB with Anti-GPNMB antibody [EPR22011-47] ab235873 at 1/500 (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
  

  Negative control: HeLa (PMID: 20056711).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-GPNMB antibody [EPR22011-47] ab235873).

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  Western blot - Anti-GPNMB antibody [EPR22011-47] - BSA and Azide free (ab236211)

  This data was developed using Anti-GPNMB antibody [EPR22011-47] ab235873, the same antibody clone in a different buffer formulation.

  Anti-GPNMB antibody [EPR22011-47] ab235873 was shown to react with GPNMB in wild-type U-87 MG cells in Western blot with loss of signal observed in a GPNMB siRNA knockdown cell line. Cell lysates from wild-type U-87 MG transfected with either scrambled siRNA or GPNMB siRNA were subjected to SDS-PAGE. Membranes were blocked in 5% milk in TBST for 1 hr before incubation with Anti-GPNMB antibody [EPR22011-47] ab235873 overnight at 4 °C at a 1/500 dilution. Blots were incubated with secondary antibodies at 0.2 µg/mL before imaging.
  
  This data was 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-GPNMB antibody [EPR22011-47] (Anti-GPNMB antibody [EPR22011-47] ab235873) at 1/500 dilution

  Lane 1: Wild-type U-87 MG transfected with scrambled siRNA control lysate at 60 µg

  Lane 2: U-87 MG transfected with siRNA specifically targeting GPNMB cell lysate at 60 µg

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  Immunocytochemistry/ Immunofluorescence - Anti-GPNMB antibody [EPR22011-47] - BSA and Azide free (ab236211)

  This data was developed using Anti-GPNMB antibody [EPR22011-47] ab235873, the same antibody clone in a different buffer formulation.

  Anti-GPNMB antibody [EPR22011-47] ab235873 was shown to react with GPNMB in wild-type U-87 MG cells in immunocytochemistry with loss of signal observed in a GPNMB siRNA knockdown cell line. Wild-type and siRNA knockdown 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 1x PBS, 0.01% Triton X-100, 5% BSA, 5% NGS. The cells were then incubated with Anti-GPNMB antibody [EPR22011-47] ab235873 at 1/250 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 ?g/ml. Acquisition of the green (wild-type), red (antibody staining) and far-red (siRNA knockdown) channels was performed. Representative grayscale images of the red channel are shown. Wild-type and siRNA knockdown 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).
  
  This data was 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.