Cell Signaling Technology

HIF-1 alpha Antibody

#3716 · western blot · $317

66
Evidence Score · Well-Established
Used by 373 independent labs across 408 papers. How we score this →
100
Citing papers
9.9k
Combined citations
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Research areas

Cytokine Signaling Pathways and Interactions8Glycosylation and Glycoproteins Research7Cancer Cells and Metastasis6MicroRNA in disease regulation6Ubiquitin and proteasome pathways5Histone Deacetylase Inhibitors Research5Monoclonal and Polyclonal Antibodies Research5Autophagy in Disease and Therapy4

Papers citing this product

1
Liver‐specific deletion of histone deacetylase 3 disrupts metabolic transcriptional networks
The EMBO Journal·2008·265 cit.·DOI
2
Metabolic reprogramming induced by ketone bodies diminishes pancreatic cancer cachexia
Cancer & Metabolism·2014·253 cit.·DOI
3
Preconditioning of bone marrow-derived mesenchymal stem cells highly strengthens their potential to promote IL-6-dependent M2b polarization
Stem Cell Research & Therapy·2018·229 cit.·DOI
4
Interaction with FcγRIIB Is Critical for the Agonistic Activity of Anti-CD40 Monoclonal Antibody
The Journal of Immunology·2011·226 cit.·DOI
5
MicroRNA-497 targets insulin-like growth factor 1 receptor and has a tumour suppressive role in human colorectal cancer
Oncogene·2012·218 cit.·DOI
6
Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK–STAT pathway in Sézary syndrome
Nature Communications·2015·202 cit.·DOI
7
Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease
PLoS Genetics·2006·189 cit.·DOI
8
SOX2 Gene Regulates the Transcriptional Network of Oncogenes and Affects Tumorigenesis of Human Lung Cancer Cells
PLoS ONE·2012·163 cit.·DOI
9
Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia
Journal of Neuroscience·2017·163 cit.·DOI
10
Group-Based Optimization of Potent and Cell-Active Inhibitors of the von Hippel–Lindau (VHL) E3 Ubiquitin Ligase: Structure–Activity Relationships Leading to the Chemical Probe (2<i>S</i>,4<i>R</i>)-1-((<i>S</i>)-2-(1-Cyanocyclopropanecarboxamido)-3,3-dimethylbutanoyl)-4-hydroxy-<i>N</i>-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide (VH298)
Journal of Medicinal Chemistry·2017·161 cit.·DOI

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