Anti-Vimentin 抗体 [SP20]

• ICC/IF

Supplier Data

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.

This image is courtesy of an anonymous Abreview

• Flow Cyt

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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).

• ICC/IF

Lab

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 ab195889 at 1/250 dilution (shown in pseudo-color red) overnight at +4°C. The cells were then incubated with 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).

• IHC-P

Supplier Data

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.

• Flow Cyt

Unknown

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) (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.

• ICC/IF

Supplier Data

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.

This image is courtesy of an Abreview submitted by Miss Szu-Yu Chen

• WB

Lab

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] (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 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

Observed band size: 55 kDa

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• WB

Unknown

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, 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 ab255446 (knockout cell lysate ab263775) was used. Wild-type and Vimentin knockout samples were subjected to SDS-PAGE. ab16700 and 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 (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.

Lanes 1 - 4:

Western blot - Anti-Vimentin antibody [SP20], prediluted (<a href='/products/primary-antibodies/vimentin-antibody-sp20-prediluted-ab27608'>ab27608</a>) 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 (<a href='/products/cell-lines/human-vim-vimentin-knockout-hela-cell-line-ab255446'>ab255446</a>)

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 (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/20000 dilution

Predicted band size: 53 kDa

Observed band size: 37 kDa,53 kDa

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• WB

CiteAb

Western blot - Anti-Vimentin antibody [SP20] (AB16700)

Western Blotting using Anti-Vimentin antibody [SP20], ab16700. Publication image from Loewer, A. et al., 2014, Nat Commun, 25392082. Legend direct from paper.

Chlamydia induces p53 degradation.(a) Western blotting analysis showing progressive degradation of totalp53 protein between24 and 48 h p.i. in CTL2-infected whole-cell lysates(MOI=1). Chlamydial Hsp60and β-actinserved as infection and loading controls, respectively. (b)Representative time-lapse microscopy images of p53-Venus-expressing cells infectedwith CTL2 (MOI=0.5) from 24 to 40 h p.i. Nuclei from infected anduninfected cells are presented as montages as indicated. (c)Individual cells were tracked and the average nuclear Venus fluorescence (ingreen) measured. Normalized trajectories of p53-Venus levels are shown.Vertical dashed line indicates time of cell division. Scale bar,20 µm. (d) The fraction of cells showing nopulse, 1 or 2 pulses or more than 3 pulses between 24 and 48 hp.i. The frequency of p53pulses from >60 infected or uninfected cells were quantified. Errorbars present the standard error of the proportion. (e) Westernblotting showing decreased degradation of total p53 and non-cleavage ofkeratin 8 andvimentin inwhole-cell lysates prepared from cells infected with CTL2 (MOI=1) for48 h and treated with the proteasome inhibitors lactacystin or MG132 (150 µM)from 47 h p.i. Chlamydial Major Outer Membrane Protein (MOMP) and β-actin served asinfection and loading controls, respectively. Full blots for a ande are shown in Supplementary Fig. 7.

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