Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal HDAC1 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Mouse, Human, Rat samples. Cited in 1 publication.
View Alternative Names
RPD3L1, HDAC1, Histone deacetylase 1, HD1, Protein deacetylase HDAC1, Protein deacylase HDAC1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human testis tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on human testis is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>) at 1/1000 dilution
Lane 1:
Human fetal heart lysate at 10 µg
Lane 2:
Human fetal kidney lysate at 10 µg
Secondary
All lanes:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/4000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
Exposure time: 3min
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human prostate hyperplasia tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on luminal epithelial cells of human prostate hyperplasia, but negative staining on basal cells.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
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-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on lymphocytes of human tonsil is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed HeLa (Human epithelial cell line from cervix adenocarcinoma) cells labeling HDAC1 + HDAC2 with ab219054 at 1/700 dilution (red) compared with a rabbit monoclonal IgG isotype control (ab172730; black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human breast cancer tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on tumor cells of human breast cancer is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
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-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse colon tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on mouse colon is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
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-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human synovial sarcoma tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on human synovial sarcoma is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
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-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Nuclear staining on tumor cells of prostate cancer; weak or negative staining on basal cells.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized NIH/3T3 (Mouse embryonic fibroblast cell line) cells labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green).
Confocal image showing nuclear staining on NIH/3T3 cell line.
The nuclear counterstain is DAPI (blue).
Tubulin is detected with ab195889 (Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594)) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293 (Human epithelial cell line from embryonic kidney) cells labeling HDAC1 + HDAC2 with ab219054 at 1/1000 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green).
Confocal image showing nuclear staining on HEK-293 cell line.
The nuclear counterstain is DAPI (blue).
Tubulin is detected with ab195889 (Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594)) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
HDAC1 + HDAC2 was immunoprecipitated from 0.35 mg of HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab219054 at 1/30 dilution.
Western blot was performed from the immunoprecipitate using ab219054 at 1/1000 dilution.
VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HeLa whole cell lysate 10 μg (Input).
Lane 2 : ab219054 IP in HeLa whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab219054 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 1 second.
All lanes:
Immunoprecipitation - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>)
false
- WB
Supplier Data
Western blot - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : Lanes 1, 3-5 : 3 minutes; Lane 2 : 10 seconds.
All lanes:
Western blot - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>) at 1/1000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse spleen lysate at 10 µg
Lane 3:
Rat brain lysate at 10 µg
Lane 4:
Rat kidney lysate at 10 µg
Lane 5:
Rat spleen lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
- WB
Supplier Data
Western blot - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>) at 1/10000 dilution
Lane 1:
His-tagged human HDAC2 recombinant protein (aa339-488) at 0.01 µg
Lane 2:
His-tagged human HDAC1 recombinant protein (aa1-482) at 0.01 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 55 kDa
Observed band size: 22 kDa,60 kDa
false
- WB
Supplier Data
Western blot - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>) at 1/1000 dilution
Lane 1:
C6 (Rat glial tumor cell line) whole cell lysate at 10 µg
Lane 2:
RAW 264.7 (Mouse macrophage cell line transformed with Abelson murine leukemia virus) whole cell lysate at 10 µg
Lane 3:
PC-12 (Rat adrenal gland pheochromocytoma cell line) whole cell lysate at 10 µg
Lane 4:
NIH/3T3 (Mouse embryonic fibroblast cell line) whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
Exposure time: 5s
- WB
Supplier Data
Western blot - Anti-HDAC1+HDAC2 antibody [EPR20327] - BSA and Azide free (AB251562)
This data was developed using ab219054, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-HDAC1 + HDAC2 antibody [EPR20327] (<a href='/en-us/products/primary-antibodies/hdac1-hdac2-antibody-epr20327-ab219054'>ab219054</a>) at 1/2000 dilution
Lane 1:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
LNCaP (Human prostate cancer cell line) whole cell lysate at 20 µg
Lane 3:
SH-SY5Y (Human neuroblastoma cell line from bone marrow) whole cell lysate at 20 µg
Lane 4:
293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 55 kDa
Observed band size: 55 kDa
false
Exposure time: 5s
Related conjugates and formulations (10)
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Anti-HDAC1 + HDAC2 antibody [EPR20327]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-HDAC1 + HDAC2 antibody [EPR20327]
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578 PE
PE Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
HRP Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
660 APC
APC Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-HDAC1 + HDAC2 antibody [EPR20327]
-
603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-HDAC1 + HDAC2 antibody [EPR20327]
Reactivity data
Product details
ab251562 is the carrier-free version of ab219054.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
HDAC1 and HDAC2 function together as part of larger multiprotein complexes such as the Sin3 and NuRD complexes. These enzymes play key roles in the repression of gene expression. By altering the acetylation status of histones they contribute to chromatin condensation silencing certain gene areas. Their activity is necessary for proper development cell proliferation and differentiation. Scientists have observed that HDACs help maintain stem cell pluripotency and regulate cell cycle progression.
Pathways
HDAC1 and HDAC2 are integral to signaling pathways involved in DNA repair and cell cycle regulation. Specifically they impact the Notch and Wnt pathways which are essential for cell communication and cellular events like apoptosis and differentiation. Notably HDAC1 and HDAC2 interact with proteins such as Rb (retinoblastoma protein) and E2F transcription factors influencing cellular progression through the cell cycle and thereby affecting cell fate decisions.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Additional targets
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Cancer cell 39:1479-1496.e18 PubMed34653364
2021
Applications
Unspecified application
Species
Unspecified reactive species
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