Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Advanced Validation
- Recombinant
- KO Validated
- What is this?
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Rabbit Recombinant Monoclonal RBBP7 antibody. Carrier free. Suitable for ICC/IF, IP, WB, ChIP-seq, Flow Cyt (Intra), IHC-P and reacts with Mouse, Human, Rat samples.
View Alternative Names
RBAP46, RBBP7, Histone-binding protein RBBP7, Histone acetyltransferase type B subunit 2, Nucleosome-remodeling factor subunit RBAP46, Retinoblastoma-binding protein 7, Retinoblastoma-binding protein p46, RBBP-7
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Hela (Human cervix adenocarcinoma epithelial cell) cells labelling RBBP7 (RbAp46) with ab259957 at 1/600 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized RBBP7 (RbAp46) KO HAP1 cells labelling RBBP7 with ab259957 at 1/500 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing no staining in RBBP7 (RbAp46) KO HAP1 cells. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 (2 ug/ml) dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized parental HAP1 (Wildtype control Human chronic myelogenous leukemia near-haploid cell line, Right) / RBBP7 (RbAp46) KO HAP1 (Left) cells labelling RBBP7 with ab259957 at 1/600 dilution (0.1ug) (Red) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa cells labelling RBBP7 with ab259957 at 1/500 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing mainly nuclear staining in HeLa cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 (2 ug/ml) dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunohistochemical analysis of paraffin-embedded Human lung cancer tissue labeling RBBP7 with abab259957 at 1/2000 dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining in human lung cancer (PMID : 19655816).The section was incubated with ab259957 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- ChIP-seq
Supplier Data
ChIP-sequencing - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Chromatin was prepared from HeLa cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 10^7 HeLa cells and 8 μg of ab259957 [EPR23796-74]. 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.
- ChIP-seq
Supplier Data
ChIP-sequencing - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Chromatin was prepared from HeLa cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 HeLa cells and 3 μg of ab259957 [EPR23796-74]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. At time of publication of this image, ChIP-seq was not widely characterised in HeLa for this antibody. For any questions, please contact Abcam Technical Support. Additional screenshots of mapped reads can be downloaded here.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunohistochemical analysis of paraffin-embedded Rat lung tissue labeling RBBP7 with abab259957 at 1/2000 dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining in rat lung (PMID : 19655816). The section was incubated with ab259957 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NIH/3T3 (Mouse embryonic fibroblast) cells labelling RBBP7 (RbAp46) with ab259957 at 1/600 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labeling RBBP7 with abab259957 at 1/2000 dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining in mouse lung (PMID : 19655816). The section was incubated with ab259957 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized NIH/3T3 cells labelling RBBP7 with ab259957 at 1/500 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing mainly nuclear staining in NIH/3T3 cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 (2 ug/ml) dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
- WB
Lab
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure times : 8 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
All lanes:
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>) at 1/1000 dilution
Lane 1:
Jurkat (human t cell leukemia t lymphocyte) whole cell lysate at 20 µg
Lane 2:
MCF7 (human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
LNCaP (human prostate carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 5:
F9 (mouse embryonal carcinoma epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 48 kDa
Observed band size: 48 kDa
false
- WB
Lab
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure times : Lanes 1-3 : 3 minutes; Lane 4 : 3 seconds; Lanes 5-6 : 3 minutes; Lane 7-11 : 3 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
All lanes:
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>) at 1/1000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse heart tissue lysate at 20 µg
Lane 3:
Mouse liver tissue lysate at 20 µg
Lane 4:
Mouse spleen tissue lysate at 20 µg
Lane 5:
Rat heart tissue lysate at 20 µg
Lane 6:
Rat kidney tissue lysate at 20 µg
Lane 7:
Rat spleen tissue lysate at 20 µg
Lane 8:
C6 (rat glial tumor glial cell) whole cell lysate at 20 µg
Lane 9:
RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 10:
PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 20 µg
Lane 11:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 48 kDa
Observed band size: 48 kDa
false
- IP
Unknown
Immunoprecipitation - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
RBBP7 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with ab259957 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab259957 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 ug
Lane 2 : abab259957 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab259957 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 24 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
All lanes:
Immunoprecipitation - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>)
Predicted band size: 48 kDa
Observed band size: 48 kDa
false
- IP
Unknown
Immunoprecipitation - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
RBBP7 was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast) whole cell lysate with ab259957 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab259957 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 10 ug
Lane 2 : abab259957 IP in NIH/3T3 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab259957 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 24 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
All lanes:
Immunoprecipitation - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>)
Predicted band size: 48 kDa
Observed band size: 48 kDa
false
- WB
Lab
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
ab259957 was shown to specifically react with RBBP7 in wild-type HAP1 cells as signal was lost in RBBP7 (RbAp46) knockout cells.
Wild-type and RBBP7 (RbAp46) knockout samples were subjected to SDS-PAGE. ab259957 and ab181602 (Rabbit anti-GAPDH loading control) were incubated 1 hour at room temperature at 1/2000 dilution and 1/200,000 dilution respectively. Blots were developed with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) secondary antibody at 1/50,000 dilution for 1 hour at room temperature before imaging. The blot was developed on a BIO-RAD® ChemiDoc™ MP instrument using the ECL technique.
Exposure time : 10 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab259957).
All lanes:
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>) at 1/2000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
RBBP7 (RbAp46) knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 48 kDa
Observed band size: 48 kDa
false
- WB
Lab
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade - BSA and Azide free (AB273882)
This data was developed using the same antibody clone in a different buffer formulation (ab259957).
Lanes 1 - 2 : Merged signal (red and green). Green - ab259957 observed at 50 kDa. Red - loading control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37 kDa.
ab259957 was shown to react with RBBP7 in wild-type HeLa cells in Western blot with loss of signal observed in RBBP7 knockout cell line ab264677 (RBBP7 knockout cell lysate ab258628). Wild-type HeLa and RBBP7 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3 % milk in TBS-T (0.1 % Tween®) before incubation with ab259957 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4 °C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-RBBP7 antibody [EPR23796-74] - ChIP Grade (<a href='/en-us/products/primary-antibodies/rbbp7-antibody-epr23796-74-chip-grade-ab259957'>ab259957</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
RBBP7 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human RBBP7 (RbAp46) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-rbbp7-rbap46-knockout-hela-cell-line-ab264677'>ab264677</a>)
Predicted band size: 48 kDa
Observed band size: 50 kDa
false
Reactivity data
Product details
ab273882 is the carrier-free version of ab259957.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com