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AB1440

Anti-HDAC6 antibody

3

(3 Reviews)

|

(38 Publications)

Rabbit Polyclonal HDAC6 antibody. Suitable for WB and reacts with Human samples. Cited in 38 publications. Immunogen corresponding to Synthetic Peptide within Mouse Hdac6.

View Alternative Names

KIAA0901, JM21, HDAC6, Histone deacetylase 6, HD6, Protein deacetylase HDAC6, Tubulin-lysine deacetylase HDAC6

1 Images
Western blot - Anti-HDAC6 antibody (AB1440)
  • WB

Unknown

Western blot - Anti-HDAC6 antibody (AB1440)

All lanes:

Western blot - Anti-HDAC6 antibody (ab1440)

All lanes:

Jurkat cell lysate

Predicted band size: 131 kDa

Observed band size: 131 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

Synthetic Peptide within Mouse Hdac6. The exact immunogen used to generate this antibody is proprietary information.

Q9Z2V5

Specificity

The antibody detects ~134 kDa histone deacetylase 6. It does not cross-react with other HDAC proteins including HDAC1, 2, 3, 4, 5, 7, and 8.

Reactivity data

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Product details

This product is manufactured by BioVision, an Abcam company and was previously called 3606 HDAC6 Antibody.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
Preservative: 0.02% Sodium azide Constituents: 50% Glycerol (glycerin, glycerine), 1% BSA
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.

HDAC6 or histone deacetylase 6 is a protein that primarily functions as a cytoplasmic deacetylase. It is part of the class IIb HDAC family and is known for its distinctive molecular weight of approximately 121 kDa. HDAC6 is expressed in various tissues with higher levels observed in the brain kidney and liver. This protein is unique as it contains two catalytic domains unlike other HDACs which contributes to its specific deacetylation of non-histone substrates including tubulin and Hsp90 influencing cell motility and stress response.
Biological function summary

HDAC6 plays a significant role in processes like protein degradation and cell signaling. It is an important component of the protein quality control system involving itself in the aggresome pathway where it facilitates the removal of misfolded proteins through interaction with dynein motor proteins. In addition to its presence in the cytoplasm HDAC6 influences cell migration and immune response regulation by de-phosphorylating cortactin and affecting actin filament dynamics. Its integral role in the aggresome-autophagy pathway positions it as important for cellular homeostasis maintenance.

Pathways

HDAC6 participates prominently in both autophagy and stress response pathways. In the autophagic process HDAC6 operates alongside ubiquitinated proteins to manage protein quality control. Moreover HDAC6 engages in stress response pathways like the heat shock response interacting directly with Hsp90 to regulate client protein activation. These pathways highlight HDAC6’s relationships with key proteins such as Hsp70 and tau linking it to cellular stress and neurodegeneration responses.

HDAC6 exhibits connections to neurodegenerative diseases and cancer. Dysregulated HDAC6 activity associates with Alzheimer's disease where it affects tau protein accumulation and degradation. The protein is also implicated in various cancers such as breast and ovarian cancer due to its influence on cell migration and invasion. It interacts with p53 impacting apoptosis and tumor progression making HDAC6 a potential target for therapeutic interventions with HDAC6 inhibitors which aim to restore normal cellular functions disrupted by abnormal HDAC6 activity.

Product protocols

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

Target data

Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) (PubMed : 10220385). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events (PubMed : 10220385). Histone deacetylases act via the formation of large multiprotein complexes (PubMed : 10220385). In addition to histones, deacetylates other proteins, such as CTTN, tubulin and SQSTM1 (PubMed : 12024216, PubMed : 20308065, PubMed : 26246421, PubMed : 30538141, PubMed : 31857589). Plays a central role in microtubule-dependent cell motility by mediating deacetylation of tubulin (PubMed : 12024216, PubMed : 20308065, PubMed : 26246421). Required for cilia disassembly; via deacetylation of alpha-tubulin (PubMed : 17604723, PubMed : 26246421). Promotes deacetylation of CTTN, leading to actin polymerization, promotion of autophagosome-lysosome fusion and completion of autophagy (PubMed : 30538141). Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer (PubMed : 24413532). Promotes odontoblast differentiation following IPO7-mediated nuclear import and subsequent repression of RUNX2 expression (By similarity). In addition to its protein deacetylase activity, plays a key role in the degradation of misfolded proteins : when misfolded proteins are too abundant to be degraded by the chaperone refolding system and the ubiquitin-proteasome, mediates the transport of misfolded proteins to a cytoplasmic juxtanuclear structure called aggresome (PubMed : 17846173). Probably acts as an adapter that recognizes polyubiquitinated misfolded proteins and target them to the aggresome, facilitating their clearance by autophagy (PubMed : 17846173).
See full target information HDAC6

Publications (38)

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

Science advances 11:eadu7602 PubMed40498831

2025

Influenza A virus subverts the LC3-pericentrin dynein adaptor complex for host cytoplasm entry.

Applications

Unspecified application

Species

Unspecified reactive species

Yingying Cong,Pauline Verlhac,Benjamin B Green,Jacqueline de Vries-Idema,Line Moesgaard Strauss,Clàudia Río-Bergé,Anders Etzerodt,Lene N Nejsum,Anke L W Huckriede,Fulvio Reggiori

Acta biochimica et biophysica Sinica 56:96-105 PubMed38105649

2023

Endoplasmic reticulum stress caused by traumatic injury promotes cardiomyocyte apoptosis through acetylation modification of GRP78.

Applications

Unspecified application

Species

Unspecified reactive species

Zi Yan,Yufeng Liu,Bowen Yang,Wenhui Zhao,Yan Wang,Deping Wang,Jianguo Li,Xiangying Jiao,Jimin Cao

Cells 12: PubMed37759454

2023

HDAC6 and ERK/ADAM17 Regulate VEGF-Induced NOTCH Signaling in Lung Endothelial Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Sheng Xia,Heather L Menden,Sherry M Mabry,Venkatesh Sampath

Journal of cardiovascular pharmacology 81:150-164 PubMed36607630

2023

HDAC Inhibitors Alleviate Uric Acid-Induced Vascular Endothelial Cell Injury by Way of the HDAC6/FGF21/PI3K/AKT Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Kaihao Wang,Youhong Zhang,Min Zhou,Yipeng Du,Peixin Li,Chang Guan,Zheng Huang

Molecular oncology 16:2235-2259 PubMed35167193

2022

ARID1A-deficient cells require HDAC6 for progression of endometrial carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Cristina Megino-Luque,Pol Sisó,Natalia Mota-Martorell,Raúl Navaridas,Inés de la Rosa,Izaskun Urdanibia,Manel Albertí-Valls,Maria Santacana,Miquel Pinyol,Núria Bonifaci,Anna Macià,David Llobet-Navas,Sònia Gatius,Xavier Matias-Guiu,Núria Eritja

Nature communications 13:875 PubMed35169129

2022

Organic anion transporter 1 is an HDAC4-regulated mediator of nociceptive hypersensitivity in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Christian Litke,Anna M Hagenston,Ann-Kristin Kenkel,Eszter Paldy,Jianning Lu,Rohini Kuner,Daniela Mauceri

Journal of cachexia, sarcopenia and muscle 13:605-620 PubMed34725961

2021

Metformin induces muscle atrophy by transcriptional regulation of myostatin via HDAC6 and FoxO3a.

Applications

Unspecified application

Species

Unspecified reactive species

Min Ju Kang,Ji Wook Moon,Jung Ok Lee,Ji Hae Kim,Eun Jeong Jung,Su Jin Kim,Joo Yeon Oh,Sang Woo Wu,Pu Reum Lee,Sun Hwa Park,Hyeon Soo Kim

International journal of molecular sciences 22: PubMed34299370

2021

Phosphorylation of H3-Thr3 by Haspin Is Required for Primary Cilia Regulation.

Applications

Unspecified application

Species

Unspecified reactive species

Roberto Quadri,Sarah Sertic,Anna Ghilardi,Diego Rondelli,Guido Roberto Gallo,Luca Del Giacco,Marco Muzi-Falconi

Anticancer research 41:1647-1654 PubMed33788761

2021

Up-regulation of HDAC6 Results in Poor Prognosis and Chemoresistance in Patients With Advanced Ovarian High-grade Serous Carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Mitsutake Yano,Mariko Miyazawa,Naoki Ogane,Aiko Ogasawara,Kosei Hasegawa,Hisashi Narahara,Masanori Yasuda

Toxicology and industrial health 36:759-768 PubMed32783763

2020

Carbon black nanoparticles induce HDAC6-mediated inflammatory responses in 16HBE cells.

Applications

Unspecified application

Species

Unspecified reactive species

Hui Lin,Guoqing Fu,Qimei Yu,Zhenyu Wang,Yao Zuo,Yuqin Shi,Ling Zhang,Yingying Gu,Lingzhi Qin,Ting Zhou
View all publications

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