Anti-Vimentin antibody [SP20]

9 product images

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  This image is courtesy of an anonymous customer review

  Immunocytochemistry/ Immunofluorescence - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  
  ab16700 staining Vimentin in human corneal limbal epithelial cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde and permeabilized with 0.3% Triton X-100 for 5 minutes. Samples were incubated with primary antibody (1/200 in PBS + 10% normal goat serum) for 18 hours at 4°C. An Alexa Fluor®488-conjugated goat anti-rabbit IgG polyclonal (1/500) was used as the secondary antibody.
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  Flow Cytometry - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  
  Flow cytometric analysis of rabbit anti-Vimentin (SP20) antibody ab16700 (1/100) in HeLa cells (green) compared to negative control of rabbit IgG (blue).
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  Western blot - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  Lanes 1 - 4: Merged signal (red and green). Green - ab16700 observed at 53 kDa. Red - loading control, Anti-GAPDH antibody [6C5] - Loading Control ab8245 observed at 37 kDa.
  

  ab16700 was shown to react with Vimentin in wild-type HeLa cells. Loss of signal was observed when knockout cell line Human VIM (Vimentin) knockout HeLa cell line ab255446 (knockout cell lysate Human VIM (Vimentin) knockout HeLa cell lysate ab263775) was used. Wild-type and Vimentin knockout samples were subjected to SDS-PAGE. ab16700 and Anti-GAPDH antibody [6C5] - Loading Control (Anti-GAPDH antibody [6C5] - Loading Control ab8245) were incubated overnight at 4°C at 1 in 100 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.

  Lanes 1 - 4: Western blot - Anti-Vimentin antibody [SP20], prediluted (Anti-Vimentin antibody [SP20], prediluted ab27608) at 1/100 dilution

  Lanes 1 - 4: Western blot - Anti-Vimentin antibody [SP20] (ab16700) at 1/100 dilution

  Lane 1: U20S cell lysate at 20 µg

  Lane 2: Human tonsil cell lysate at 20 µg

  Lane 2: Western blot - Human VIM (Vimentin) knockout HeLa cell line (Human VIM (Vimentin) knockout HeLa cell line ab255446)

  Lane 3: Wild-type HeLa cell lysate at 20 µg

  Lane 4: VIM knockout HeLa cell lysate at 20 µg

  Secondary

  All lanes: Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) at 1/20000 dilution

  Performed under reducing conditions.

  Predicted band size: 53 kDa

  Observed band size: 37 kDa, 53 kDa

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  Flow Cytometry - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  Overlay histogram showing HeLa cells stained with ab16700 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab16700, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x10⁶ cells) used under the same conditions. Acquisition of >5,000 events was performed.

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  Western blot - Anti-Vimentin antibody [SP20] (ab16700)

  Lane 1: Anti-MDM2 antibody [4B11] (ab16900) at 1/100 dilution

  Lane 1: Western blot - Anti-Vimentin antibody [SP20] (ab16700) at 1/100 dilution

  All lanes: HeLa cell lysate

  Predicted band size: 53 kDa

  Observed band size: 53 kDa

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  Immunocytochemistry/ Immunofluorescence - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  ab16700 staining Vimentin in wild-type HAP1 cells (top panel) and Vimentin knockout HAP1 cells (bottom panel). The cells were fixed with 100% methanol (5min), permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab16700 at 1/1000 dilution and Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 at 1/250 dilution (shown in pseudo-color red) overnight at +4°C. The cells were then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 (Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 488)) at 1/1000 dilution for 1 hour. Nuclear DNA was labelled in blue with DAPI.

  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

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  This image is courtesy of a customer review submitted by Miss Szu-Yu Chen

  Immunocytochemistry/ Immunofluorescence - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  ab16700 at 1/200 staining Human Limbal Epithelial Cells by ICC/IF. The cells were incubated with the antibody for 1 hour and then a FITC conjugated goat antibody was used as the secondary. The image shows vimentin staining in green and hoechst staining in blue. The upper cells in the image (vimentin negative) are epithelium cells. the vimentin positive cells are stroma cells.

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  Western blot - Anti-Vimentin antibody [SP20] (ab16700)

  This image was generated using a previous batch manufactured using the hybridoma production method.

  False colour image of Western blot: Anti-Vimentin antibody [SP20] staining at 1/120 dilution, shown in green; Mouse anti-CANX [CANX/1543] (Anti-Calnexin antibody [CANX/1543] ab238078) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab16700 was shown to bind specifically to Vimentin. A band was observed at 55 kDa in wild-type A549 cell lysates with no signal observed at this size in VIM knockout cell line Human VIM knockout A549 cell line ab288984. To generate this image, wild-type and VIM knockout A549 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 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.

  All lanes: Western blot - Anti-Vimentin antibody [SP20] (ab16700) at 1/120 dilution

  Lane 1: Wild-type A549 cell lysate at 20 µg

  Lane 2: Vimentin knockout A549 cell lysate at 20 µg

  Lane 3: Daudi cell lysate at 20 µg

  Performed under reducing conditions.

  Observed band size: 55 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Vimentin antibody [SP20] (ab16700)

  Immunohistochemical analysis of paraffin-embedded Human melanoma tissue labeling Vimentin with ab16700 at 1/200 dilution. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.