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AB61058

Anti-HDAC6 (phospho S22) 抗体

Anti-HDAC6 (phospho S22) antibody

4

(7 Reviews)

|

(5 Publications)

Rabbit Polyclonal HDAC6 phospho S22 antibody. Suitable for IHC-P and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Synthetic Peptide within Human HDAC6 pS22 aa 1-100.

別名を表示する

KIAA0901, JM21, HDAC6, Protein deacetylase HDAC6, E3 ubiquitin-protein ligase HDAC6, Tubulin-lysine deacetylase HDAC6

1 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HDAC6 (phospho S22) antibody (AB61058)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HDAC6 (phospho S22) antibody (AB61058)

Immunohistochemistry analysis of paraffin-embedded human testis tissue using HDAC6 (phospho S22) antibody (ab61058) at 1/50 - 1/100 dilution, in the presence (right panel) and absence (left panel) of phosphopeptide.

Key facts

宿主種

Rabbit

クローン性

Polyclonal

アイソタイプ

IgG

キャリアフリー

No

交差種

Human

アプリケーション

IHC-P

applications

免疫原

Synthetic Peptide within Human HDAC6 pS22 aa 1-100. The exact immunogen used to generate this antibody is proprietary information.

Q9UBN7

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "1/50 - 1/100", "IHCP-species-notes": "<p></p>" } } }

出荷温度及び保存条件

製品の状態
Liquid
精製方法
Affinity purification Immunogen
精製に関する特記事項
ab61058 was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide was removed by chromatography using non-phosphopeptide corresponding to the phosphorylation site.
バッファー組成
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 50% Glycerol (glycerin, glycerine), 0.87% Sodium chloride
出荷温度
Blue Ice
短期保存温度
+4°C
長期保存温度
-20°C
保管に関する情報
Stable for 12 months at -20°C

補足情報

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.

製品プロトコール

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ターゲットの情報

Deacetylates a wide range of non-histone substrates (PubMed : 12024216, PubMed : 18606987, PubMed : 20308065, PubMed : 24882211, PubMed : 26246421, PubMed : 30538141, PubMed : 31857589, PubMed : 30770470, PubMed : 38534334, PubMed : 39567688). 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). Alpha-tubulin deacetylation results in destabilization of dynamic microtubules (By similarity). Promotes deacetylation of CTTN, leading to actin polymerization, promotion of autophagosome-lysosome fusion and completion of autophagy (PubMed : 30538141). Deacetylates SQSTM1 (PubMed : 31857589). Deacetylates peroxiredoxins PRDX1 and PRDX2, decreasing their reducing activity (PubMed : 18606987). Deacetylates antiviral protein RIGI in the presence of viral mRNAs which is required for viral RNA detection by RIGI (By similarity). Sequentially deacetylates and polyubiquitinates DNA mismatch repair protein MSH2 which leads to MSH2 degradation, reducing cellular sensitivity to DNA-damaging agents and decreasing cellular DNA mismatch repair activities (PubMed : 24882211). Deacetylates DNA mismatch repair protein MLH1 which prevents recruitment of the MutL alpha complex (formed by the MLH1-PMS2 heterodimer) to the MutS alpha complex (formed by the MSH2-MSH6 heterodimer), leading to tolerance of DNA damage (PubMed : 30770470). Deacetylates RHOT1/MIRO1 which blocks mitochondrial transport and mediates axon growth inhibition (By similarity). Deacetylates transcription factor SP1 which leads to increased expression of ENG, positively regulating angiogenesis (PubMed : 38534334). Deacetylates KHDRBS1/SAM68 which regulates alternative splicing by inhibiting the inclusion of CD44 alternate exons (PubMed : 26080397). Deacetylates PRDM16 (By similarity). Acts as a valine sensor by binding to valine through the primate-specific SE14 repeat region (PubMed : 39567688). In valine deprivation conditions, translocates from the cytoplasm to the nucleus where it deacetylates TET2 which promotes TET2-dependent DNA demethylation, leading to DNA damage (PubMed : 39567688). 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 targets them to the aggresome, facilitating their clearance by autophagy (PubMed : 17846173). Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer (PubMed : 24413532).. (Microbial infection) Deacetylates the SARS-CoV-2 N protein which promotes association of the viral N protein with human G3BP1, leading to disruption of cellular stress granule formation and facilitating viral replication.
See full target information HDAC6 pS22

文献 (5)

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

Cell reports 35:109037 PubMed33910013

2021

Tau seeds are subject to aberrant modifications resulting in distinct signatures.

Applications

Unspecified application

Species

Unspecified reactive species

Jui-Heng Tseng,Aditi Ajit,Zarin Tabassum,Niyati Patel,Xu Tian,Youjun Chen,Alex W Prevatte,Karen Ling,Frank Rigo,Rick B Meeker,Laura E Herring,Todd J Cohen

Aging 12:25581-25598 PubMed33231564

2020

A dual inhibitor targeting HMG-CoA reductase and histone deacetylase mitigates neurite degeneration in parkinsonism.

Applications

Unspecified application

Species

Unspecified reactive species

Chin-Hsien Lin,Han-Yi Lin,Jim-Min Fang,Ching-Chow Chen

Molecular cancer research : MCR 17:225-237 PubMed30224543

2018

The Role of Alcohol-Induced Golgi Fragmentation for Androgen Receptor Signaling in Prostate Cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Sonia Manca,Cole P Frisbie,Chad A LaGrange,Carol A Casey,Jean-Jack M Riethoven,Armen Petrosyan

American journal of physiology. Heart and circulatory physiology 312:H446-H458 PubMed28011589

2016

Maternal-engineered nanomaterial exposure disrupts progeny cardiac function and bioenergetics.

Applications

Unspecified application

Species

Unspecified reactive species

Quincy A Hathaway,Cody E Nichols,Danielle L Shepherd,Phoebe A Stapleton,Sarah L McLaughlin,Janelle C Stricker,Stephanie L Rellick,Mark V Pinti,Alaeddin B Abukabda,Carroll R McBride,Jinghai Yi,Seth M Stine,Timothy R Nurkiewicz,John M Hollander

PloS one 5:e10848 PubMed20520769

2010

HDAC6 regulates mitochondrial transport in hippocampal neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Sigeng Chen,Geoffrey C Owens,Helen Makarenkova,David B Edelman
View all publications

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