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AB7028

Anti-HDAC1 antibody - Nuclear Loading Control

4

(24 Reviews)

|

(255 Publications)

Anti-HDAC1 antibody (ab7028) is a rabbit polyclonal antibody detecting HDAC1 in Western Blot, IP, ICC/IF. Suitable for Chinese hamster, Human, Mouse, Rat.

- Over 240 publications
- Trusted since 2002

View Alternative Names

RPD3L1, HDAC1, Histone deacetylase 1, HD1, Protein deacetylase HDAC1, Protein deacylase HDAC1

7 Images
Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • WB

AbReview12302****

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

All lanes:

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (ab7028) at 1/1000 dilution

Lane 1:

Whole cell lysate from human HEK293 cell line at 20 µg

Lane 2:

Whole cell lysate from human HEK293 cell line treated with HDAC1 gene silencing shRNA at 20 µg

Secondary

All lanes:

HRP-conjugated goat anti-rabbit Ig at 1/5000 dilution

Predicted band size: 55 kDa

true

Exposure time: 10s

This image is courtesy of an anonymous Abreview

Immunocytochemistry/ Immunofluorescence - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

Immunofluorescence analysis of methanol fixed HeLa cells with ab7028 labelling HDAC1 at 1/200 dilution. The antibody was developed using Goat Anti-Rabbit IgG, Cy3 conjugate.

Immunocytochemistry/ Immunofluorescence - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • ICC/IF

PubMed

Immunocytochemistry/ Immunofluorescence - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

MCF-7 cells were treated with indicated concentrations of panobinostat (optical sections A-D, respectively) or trichostatin A (optical sections E-H, respectively) for 12 hours, fixed, permeabilized and optical sections were obtained by laser scanning confocal microscopy. Fluorescence signal for HDAC1 is shown in green (left panels), DAPI staining is shown in blue (middle panels), and merged optical sections are shown in the right panels. Colocalization analysis of HDAC1 fluorescence signal and the DAPI stain signal was performed with JACoP (ImageJ).

HDAC1 was detected with ab7028. cells were ficed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100.

(After Figure 3 of Hanigan et al).

Hanigan, T.W. et al Send to PLoS One. 2017 Oct 18;12(10):e0186620. doi: 10.1371/journal.pone.0186620. eCollection 2017 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • IP

Supplier Data

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

HDAC1 was immunoprecipitated from HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell extract with ab7028.

Lane 1 : 5 μl ab7028 in HeLa whole cell lysate.

Lane 2 : 10 μl ab7028 in HeLa whole cell lysate.

Lane 3 : 10 μl control antibody in HeLa whole cell lysate.

All lanes:

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (ab7028)

Predicted band size: 55 kDa

false

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • IP

Unknown

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

HDAC1 was immunoprecipitated using 0.5mg Hela whole cell extract, 5μg of Rabbit polyclonal to HDAC1 and 50μl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, Hela whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40μl SDS loading buffer and incubated for 10min at 70°C; 10μl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab7028.
Secondary : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
Band : 60ka : HDAC1.

All lanes:

Immunoprecipitation - Anti-HDAC1 antibody - Nuclear Loading Control (ab7028)

Predicted band size: 55 kDa

false

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • WB

Supplier Data

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

All lanes:

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (ab7028) at 1/10000 dilution

Lane 1:

HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) cell lysate

Lane 2:

HeLa (human epithelial cell line from cervix adenocarcinoma) cell lysate

Lane 3:

K562 (human chronic myelogenous leukemia cell line from bone marrow ) cell lysate

Lane 4:

CHO (Chinese hamster ovary cell line) cell lysate

Lane 5:

NIH/3T3 (mouse embryo fibroblast cell line) cell lysate

Lane 6:

PC-12 (rat adrenal gland pheochromocytoma cell line) cell lysate

Secondary

All lanes:

Goat Anti-Rabbit HRP

Predicted band size: 55 kDa

false

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)
  • WB

AbReview29619****

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (AB7028)

Blocked with 5% milk for 1 hour at 20°C

All lanes:

Western blot - Anti-HDAC1 antibody - Nuclear Loading Control (ab7028) at 1/2000 dilution

All lanes:

Human HuH-7 whole cell lysate at 15 µg

Secondary

All lanes:

HRP conjugated Sheet anti-rabbit IgG polyclonal at 1/20000 dilution

Predicted band size: 55 kDa

true

Exposure time: 20s

This image is courtesy of an anonymous Abreview

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human, Chinese hamster, Mouse, Rat

Applications

ICC/IF, WB, IP

applications

Immunogen

Synthetic Peptide within Human HDAC1 aa 450 to C-terminus conjugated to Keyhole Limpet Haemocyanin. The exact immunogen used to generate this antibody is proprietary information.

Q13547

Reactivity data

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Product details

What is this antibody validated in?
Anti-HDAC1 antibody (ab7028) is a rabbit polyclonal antibody and is validated for use in Western Blot (WB), Immunoprecipitation (IP), Immunocytochemistry/immunofluorescence (ICC/IF) in Chinese hamster, Human, Mouse, Rat samples.

What is the molecular weight of HDAC1?
Anti-HDAC1 (ab7028) specifically detects a band for HDAC1 (UniProt: Q13547) at a molecular weight of 55kDa.

Trusted by the scientific community
Anti-HDAC1 (ab7028) was first used in a scientific publication in 2002 and has been cited over 240 times in peer-reviewed journals.

Reviewed by scientists
Anti-HDAC1 (ab7028) has over 20 independent reviews from customers.

Properties and storage information

Form
Liquid
Purity
IgG fraction
Purification notes
Whole antiserum is fractionated and further purified by anion-exchange chromatography to provide the IgG fraction of antiserum that is essentially free of other rabbit serum proteins.
Storage buffer
pH: 7.4 Preservative: 0.097% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

HDAC1 also known as Histone Deacetylase 1 is a member of the histone deacetylase family with a molecular weight of approximately 55 kDa. Mechanically HDAC1 removes acetyl groups from lysine residues on histone proteins an action known as histone deacetylation. This process causes chromatin structure to become more compact which leads to transcriptional repression. HDAC1 is broadly expressed in various tissues particularly in the brain heart and kidneys and is vital for cellular development and differentiation.
Biological function summary

The enzymatic activity of histone deacetylase effectively controls gene expression. HDAC1 participates as a part of the multiprotein complexes including SIN3 and NuRD which play vital roles in the regulation of transcription. By altering the acetylation state of histones HDAC1 influences chromatin remodeling thereby affecting the accessibility of transcription factors to DNA and controlling genes necessary for cell cycle progression and proliferation.

Pathways

The function of HDAC1 fits into the regulation of the cell cycle and apoptosis pathways. In the cell cycle pathway HDAC1 interacts with other histone deacetylases (HDACs) and plays a role in controlling the progression of the cell division. The interplay between HDAC1 and proteins such as p53 further showcases its regulatory activity in apoptosis ensuring cell survival or programmed cell death when necessary.

HDAC1 shows significant relevance to cancer and neurodegenerative diseases. In cancer the overexpression or abnormal regulation of HDAC1 can lead to uncontrolled cell proliferation often linked to the silencing of tumor suppressor genes. Within neurodegenerative conditions HDAC1-related disturbances in gene expression may result in impaired neuronal function and survival. The involvement of HDAC1 with proteins such as p53 and other HDACs illustrates its impact on complex disease mechanisms making it a critical target for therapeutic interventions.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Histone deacetylase that catalyzes the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) (PubMed : 16762839, PubMed : 17704056, PubMed : 28497810). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events (PubMed : 16762839, PubMed : 17704056). Histone deacetylases act via the formation of large multiprotein complexes (PubMed : 16762839, PubMed : 17704056). Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin (PubMed : 16428440, PubMed : 28977666). As part of the SIN3B complex is recruited downstream of the constitutively active genes transcriptional start sites through interaction with histones and mitigates histone acetylation and RNA polymerase II progression within transcribed regions contributing to the regulation of transcription (PubMed : 21041482). Also functions as a deacetylase for non-histone targets, such as NR1D2, RELA, SP1, SP3, STAT3, ZNF76 and TSHZ3 (PubMed : 12837748, PubMed : 16285960, PubMed : 16337145, PubMed : 16478997, PubMed : 17996965, PubMed : 19343227). Deacetylates SP proteins, SP1 and SP3, and regulates their function (PubMed : 12837748, PubMed : 16478997). Component of the BRG1-RB1-HDAC1 complex, which negatively regulates the CREST-mediated transcription in resting neurons (PubMed : 19081374). Upon calcium stimulation, HDAC1 is released from the complex and CREBBP is recruited, which facilitates transcriptional activation (PubMed : 19081374). Deacetylates TSHZ3 and regulates its transcriptional repressor activity (PubMed : 19343227). Deacetylates 'Lys-310' in RELA and thereby inhibits the transcriptional activity of NF-kappa-B (PubMed : 17000776). Deacetylates NR1D2 and abrogates the effect of KAT5-mediated relieving of NR1D2 transcription repression activity (PubMed : 17996965). Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development (By similarity). Involved in CIART-mediated transcriptional repression of the circadian transcriptional activator : CLOCK-BMAL1 heterodimer (By similarity). Required for the transcriptional repression of circadian target genes, such as PER1, mediated by the large PER complex or CRY1 through histone deacetylation (By similarity). In addition to protein deacetylase activity, also has protein-lysine deacylase activity : acts as a protein decrotonylase and delactylase by mediating decrotonylation ((2E)-butenoyl) and delactylation (lactoyl) of histones, respectively (PubMed : 28497810, PubMed : 35044827).
See full target information HDAC1

Publications (255)

Recent publications for all applications. Explore the full list and refine your search

Cell death & disease 16:270 PubMed40204721

2025

USP10 stabilizes BAZ1A to drive tumor stemness via an epigenetic mechanism in head and neck squamous cell carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Yanni Shi,Jiawei Ding,Xiao Ling,Danfeng Xu,Yan Shen,Xingjun Qin

Nucleic acids research 52:13706-13722 PubMed39588763

2024

Phosphorylation-mediated disassembly of C-terminal binding protein 2 tetramer impedes epigenetic silencing of pluripotency in mouse embryonic stem cells.

Applications

Unspecified application

Species

Unspecified reactive species

Han-Teo Lee,Young Ah Kim,Sangho Lee,Ye-Eun Jung,Hanbyeol Kim,Tae Wan Kim,Sojung Kwak,Jaehyeon Kim,Chul-Hwan Lee,Sun-Shin Cha,Jinmi Choi,Eun-Jung Cho,Hong-Duk Youn

Antioxidants (Basel, Switzerland) 13: PubMed39334742

2024

Multiple Mechanisms of Action of Sulfodyne, a Natural Antioxidant, against Pathogenic Effects of SARS-CoV-2 Infection.

Applications

Unspecified application

Species

Unspecified reactive species

Paul-Henri Romeo,Laurine Conquet,Sébastien Messiaen,Quentin Pascal,Stéphanie G Moreno,Anne Bravard,Jacqueline Bernardino-Sgherri,Nathalie Dereuddre-Bosquet,Xavier Montagutelli,Roger Le Grand,Vanessa Petit,Federica Ferri

iScience 27:110600 PubMed39224519

2024

HDAC1 and HDAC2 orchestrate Wnt signaling to regulate neural progenitor transition during brain development.

Applications

Unspecified application

Species

Unspecified reactive species

Yue Zhu,Yunyun Huang,Tianxiang Tang,Yunli Xie

Journal of translational medicine 22:793 PubMed39198847

2024

HDAC1 and FOXK1 mediate EGFR-TKI resistance of non-small cell lung cancer through miR-33a silencing.

Applications

Unspecified application

Species

Unspecified reactive species

Jie Liu,Wei Wang,Kunkun Wang,Wenjing Liu,Yanqiu Zhao,Xiao Han,Lin Wang,Bing-Hua Jiang

The Journal of biological chemistry 300:105695 PubMed38301894

2024

The BHLHE40‒PPM1F‒AMPK pathway regulates energy metabolism and is associated with the aggressiveness of endometrial cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Kazuo Asanoma,Hiroshi Yagi,Ichiro Onoyama,Lin Cui,Emiko Hori,Minoru Kawakami,Shoji Maenohara,Kazuhisa Hachisuga,Hiroshi Tomonobe,Keisuke Kodama,Masafumi Yasunaga,Tatsuhiro Ohgami,Kaoru Okugawa,Hideaki Yahata,Hiroyuki Kitao,Kiyoko Kato

Cancer communications (London, England) 43:1117-1142 PubMed37658635

2023

JARID2 coordinates with the NuRD complex to facilitate breast tumorigenesis through response to adipocyte-derived leptin.

Applications

Unspecified application

Species

Unspecified reactive species

Wei Liu,Yi Zeng,Xinhui Hao,Xin Wang,Jiaxiang Liu,Tianyang Gao,Mengdi Wang,Jingyao Zhang,Miaomiao Huo,Ting Hu,Tianyu Ma,Die Zhang,Xu Teng,Hefen Yu,Min Zhang,Baowen Yuan,Wei Huang,Yunkai Yang,Yan Wang

Cancer research communications 3:1716-1730 PubMed37663929

2023

Demethylation of EHMT1/GLP Protein Reprograms Its Transcriptional Activity and Promotes Prostate Cancer Progression.

Applications

Unspecified application

Species

Unspecified reactive species

Anna Besschetnova,Wanting Han,Mingyu Liu,Yanfei Gao,Muqing Li,Zifeng Wang,Maryam Labaf,Susan Patalano,Kavita Venkataramani,Rachel E Muriph,Jill A Macoska,Kellee R Siegfried,Jason Evans,Steven P Balk,Shuai Gao,Dong Han,Changmeng Cai

The Journal of experimental medicine 220: PubMed37642942

2023

A novel molecular class that recruits HDAC/MECP2 complexes to PU.1 motifs reduces neuroinflammation.

Applications

Unspecified application

Species

Unspecified reactive species

William T Ralvenius,Alison E Mungenast,Hannah Woolf,Margaret M Huston,Tyler Z Gillingham,Stephen K Godin,Jay Penney,Hugh P Cam,Fan Gao,Celia G Fernandez,Barbara Czako,Yaima Lightfoot,William J Ray,Adrian Beckmann,Alison M Goate,Edoardo Marcora,Carmen Romero-Molina,Pinar Ayata,Anne Schaefer,Elizabeta Gjoneska,Li-Huei Tsai

Nature communications 14:2983 PubMed37225693

2023

Hyperphosphorylated PTEN exerts oncogenic properties.

Applications

Unspecified application

Species

Unspecified reactive species

Janine H van Ree,Karthik B Jeganathan,Raul O Fierro Velasco,Cheng Zhang,Ismail Can,Masakazu Hamada,Hu Li,Darren J Baker,Jan M van Deursen
View all publications

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