Proteintech

HDAC1 Polyclonal antibody

#10197-1-AP · western blot · $449

70
Evidence Score · Well-Established
Used by 226 independent labs across 260 papers. How we score this →
49
Citing papers
753
Combined citations
Supplier page Find this product

Research areas

Epigenetics and DNA Methylation10RNA modifications and cancer9Cancer-related gene regulation8Histone Deacetylase Inhibitors Research7Immune cells in cancer5Genomics and Chromatin Dynamics4Cancer-related molecular mechanisms research4Cancer, Hypoxia, and Metabolism3

Papers citing this product

1
Post-translational control of beige fat biogenesis by PRDM16 stabilization
Nature·2022·109 cit.·DOI
2
Hypoxia-induced feedback of HIF-1α and lncRNA-CF129 contributes to pancreatic cancer progression through stabilization of p53 protein
Theranostics·2019·106 cit.·DOI
3
HDAC1 inhibition ameliorates TDP-43-induced cell death in vitro and in vivo
Cell Death and Disease·2020·71 cit.·DOI
4
PCGF6 controls neuroectoderm specification of human pluripotent stem cells by activating SOX2 expression
Nature Communications·2022·56 cit.·DOI
5
GCH1 induces immunosuppression through metabolic reprogramming and IDO1 upregulation in triple-negative breast cancer
Journal for ImmunoTherapy of Cancer·2021·55 cit.·DOI
6
B-lymphoid tyrosine kinase-mediated FAM83A phosphorylation elevates pancreatic tumorigenesis through interacting with β-catenin
Signal Transduction and Targeted Therapy·2023·46 cit.·DOI
7
Atf3-mediated metabolic reprogramming in hepatic macrophage orchestrates metabolic dysfunction–associated steatohepatitis
Science Advances·2024·36 cit.·DOI
8
Expression of hMOF, but not HDAC4, is responsible for the global histone H4K16 acetylation in gastric carcinoma
International Journal of Oncology·2015·33 cit.·DOI
9
LncRNA ZNFTR functions as an inhibitor in pancreatic cancer by modulating ATF3/ZNF24/VEGFA pathway
Cell Death and Disease·2021·29 cit.·DOI
10
The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots
Genome biology·2022·28 cit.·DOI

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