Anti-Histone H3 (acetyl K18) 抗体 [EPR16595] - ChIP Grade

• IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling Histone H3 (acetyl K18) with ab177870 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nucleus staining on glandular epithelium of colon tissue is observed. Counter stained with Hematoxylin.

Negative control : Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.

Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

• ICC/IF

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Immunocytochemistry/ Immunofluorescence - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling Histone H3 (acetyl K18) with ab177870 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/400 dilution (green). Confocal image showing nuclear staining on HeLa cell line. Acetylation levels increased after treatment with Trichostatin A (500 ng/ml) for 4 hours. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (Anti-alpha Tubulin antibody [DM1A] - Loading Control) at 1/500 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed (ab150120) at 1/500 dilution (red).
The negative controls are as follows;
-ve control 1 : ab177870 at 1/2000 dilution followed by ab150120 at 1/500 dilution.
-ve control 2 : ab7291 at 1/500 dilution followed by ab150077 at 1/400 dilution.

• ChIP

Supplier Data

ChIP - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Chromatin was prepared from HeLa (Human epithelial cells from cervix adenocarcinoma) cells according to the Abcam X-ChIP protocol. Cells were fixed with formaldehyde for 10min. The ChIP was performed with 25μg of chromatin, 2μg of ab177870 (blue), and 20μl of Anti rabbit IgG sepharose beads. 2μg of Rabbit normal IgG was added to the beads control (yellow). The immunoprecipitated DNA was quantified by real time PCR (SYBR approach). Primers and probes are located in the first kb of the transcribed region.

• ChIP-seq

Unknown

ChIP-sequencing - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Chromatin was prepared from HeLa cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 10^7 HeLa cells and 4 μg of ab177870 [EPR16595]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads.

Additional screenshots of mapped reads can be downloaded here.

• IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling Histone H3 (acetyl K18) with ab177870 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear staining on glandular epithelium of mouse colon tissue is observed. Counter stained with Hematoxylin.

Negative control : Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.

Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

• IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Immunohistochemical analysis of paraffin-embedded Rat cerebral cortex tissue labeling Histone H3 (acetyl K18) with ab177870 at 1/500 dilution, followed by prediluted Goat Anti-Rabbit IgG H&L (HRP). Nuclear staining on Rat cerebral cortex tissue is observed. Counter stained with Hematoxylin.

Negative control : Using PBS instead of primary antibody, secondary antibody is prediluted Goat Anti-Rabbit IgG H&L (HRP).

Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

• WB

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Western blot - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Blocking/Dilution buffer : 5% NFDM/TBST.

All lanes:

Western blot - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (ab177870) at 1/1000 dilution

Lane 1:

Whole cell lysates from HeLa (Human epithelial cells from cervix adenocarcinoma) cells treated with 500 ng/ml Trichostatin A for 4 hours at 10 µg

Lane 2:

Untreated HeLa whole cell lysates at 10 µg

Secondary

All lanes:

Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution

Predicted band size: 15 kDa

Observed band size: 15 kDa

false

• ChIC/CUT&RUN-seq

Lab

ChIC/CUT&RUN sequencing - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 HeLa (human cervical adenocarcinoma epithelial cell) cells and 5 µg of ab177870 [EPR16595]. 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-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 HeLa (human cervical adenocarcinoma epithelial cell) cells and 5 µg of ab177870 [EPR16595]. 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-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 HeLa (human cervical adenocarcinoma epithelial cell) cells and 5 µg of ab177870 [EPR16595]. 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

Supplier Data

Western blot - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Blocking/Dilution buffer : 5% NFDM/TBST.

All lanes:

Western blot - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (ab177870) at 1/1000 dilution

Lane 1:

Whole cell lysate from NIH/3T3 (Mouse embyro fibroblast cells) treated with 500 ng/ml Trichostatin A for 4 hours at 10 µg

Lane 2:

Whole cell lysates from untreated NIH/3T3 at 10 µg

Secondary

All lanes:

Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution

Predicted band size: 15 kDa

Observed band size: 15 kDa

false

• Dot

Supplier Data

Dot Blot - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

Dot blot analysis using ab177870 at 1/1000 dilution and Goat Anti-Rabbit IgG H&L (HRP) (ab97051) as secondary antibody at 1/100,000 dilution.

Lane 1 : Histone H3(acetyl K4 + K9 + K14 + K18) peptide

Lane 2 : Histone H3(acetyl K4) peptide

Lane 3 : Histone H3(acetyl K9) peptide

Lane 4 : Histone H3(acetyl K14) peptide

Lane 5 : Histone H3(acetyl K18) peptide

Lane 6 : Histone H3 unmodified peptide

Blocking and Diluting buffer and concentration : 5% NFDM/TBST

Exposure time : 10 seconds

• PepArr

Lab

Peptide Array - Anti-Histone H3 (acetyl K18) antibody [EPR16595] - ChIP Grade (AB177870)

ab177870 at 0.02 μg/mL was tested in Peptide Array against 501 different modified and unmodified histone peptides; each peptide is printed on the array at six concentrations (each in triplicate). A Goat Anti-Rabbit IgG, (H+L), Fluo 647nm conjugated at 1/50000 dilution was used as the secondary antibody. Washing buffer and time was protein Array Washing Buffer, 2*10mins and 2*5mins and blocking buffer was 5% BSA in TBST. Circle area represents affinity between the antibody and a peptide : all antigen-containing peptides are displayed as red circles, all other peptides as blue circles. The affinity is calculated as the area under the curve when antibody binding values are plotted against the corresponding peptide concentration. Each circle area is normalized to the peptide with the strongest affinity. Scanner details : Innoscan 710