Anti-INO80 antibody [EPR30384-761] - BSA and Azide free

• ICC/IF

Lab

Immunocytochemistry/ Immunofluorescence - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized A549 (human lung carcinoma epithelial cell) cells labelling INO80 with ab325542 at 1/50 (10.22 μg/ml) dilution , followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).

Confocal image showing nuclear staining in A549 cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

ab7291 Anti-alpha Tubulin mouse monoclonal antibody was used to counterstain tubulin at 1/1000 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).

Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from A549 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 µg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from A549 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 μg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from A549 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 μg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• ICC/IF

Lab

Immunocytochemistry/ Immunofluorescence - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells labelling INO80 with ab325542 at 1/50 (10.22 μg/ml) dilution , followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).

Confocal image showing mainly nuclear staining in ES-D3 [D3] cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

ab7291 Anti-alpha Tubulin mouse monoclonal antibody was used to counterstain tubulin at 1/1000 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).

Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from ES-D3 [D3] cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 μg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from ES-D3 [D3] cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 μg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• ChIP-seq

Lab

ChIP-sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Chromatin was prepared from ES-D3 [D3] cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 μg of ab325542 [EPR30384-761]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.

• WB

Lab

Western blot - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) (1 : 10000) (124KDa).

Exposure time : Lanes 1-3 : 10 seconds, lanes 4-5 : 180 seconds

All lanes:

Western blot - Anti-INO80 antibody [EPR30384-761] (<a href='/products/primary-antibodies/ino80-antibody-epr30384-761-ab325542'>ab325542</a>) at 1/1000 dilution

Lane 1:

HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 50 µg

Lane 2:

LoVo (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 50 µg

Lane 3:

SW480 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 50 µg

Lane 4:

CT26.WT (mouse colon fibroblast) whole cell lysate at 50 µg

Lane 5:

B16-F10 (mouse skin melanoma cell) whole cell lysate at 50 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 200 kDa,124 kDa

false

• WB

Lab

Western blot - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.

In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) (1 : 10000) (124KDa).

All lanes:

Western blot - Anti-INO80 antibody [EPR30384-761] (<a href='/products/primary-antibodies/ino80-antibody-epr30384-761-ab325542'>ab325542</a>) at 1/1000 dilution

Lane 1:

A549 (human lung carcinoma epithelial cell) transfected with scrambled siRNA control fresh whole cell lysate at 20 µg

Lane 2:

A549 transfected with siRNA specifically targeting INO80 fresh whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 200 kDa,170 kDa,124 kDa

false

Exposure time: 15s

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 A549 (human lung carcinoma epithelial cell) cells and 5 μg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 A549 (human lung carcinoma epithelial cell) cells and 5 µg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 A549 (human lung carcinoma epithelial cell) cells and 5 µg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

• WB

Lab

Western blot - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.

In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) (1 : 10000) (124KDa).

All lanes:

Western blot - Anti-INO80 antibody [EPR30384-761] (<a href='/products/primary-antibodies/ino80-antibody-epr30384-761-ab325542'>ab325542</a>) at 1/1000 dilution

All lanes:

ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) fresh whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 200 kDa,124 kDa

false

Exposure time: 180s

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells and 5 μg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells and 5 μg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-INO80 antibody [EPR30384-761] - BSA and Azide free (AB325543)

This data was developed using ab325542, the same antibody clone in a different buffer formulation.

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells and 5 μg of ab325542 [EPR30384-761]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown.

The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.