Related Experiment Video

Updated: Jun 6, 2026

A Quantitative Assay to Study Protein:DNA Interactions, Discover Transcriptional Regulators of Gene Expression, and Identify Novel Anti-tumor Agents
06:43

A Quantitative Assay to Study Protein:DNA Interactions, Discover Transcriptional Regulators of Gene Expression, and Identify Novel Anti-tumor Agents

Published on: August 31, 2013

Conference report: new analytical technologies for biological discovery

Hong-Wu Shen, Ai-Ming Yu

    Bioanalysis
    |November 19, 2010
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Real-time Cytotoxicity Assays in Human Whole Blood
    08:27

    Real-time Cytotoxicity Assays in Human Whole Blood

    Published on: November 7, 2014

    Related Experiment Videos

    Last Updated: Jun 6, 2026

    A Quantitative Assay to Study Protein:DNA Interactions, Discover Transcriptional Regulators of Gene Expression, and Identify Novel Anti-tumor Agents
    06:43

    A Quantitative Assay to Study Protein:DNA Interactions, Discover Transcriptional Regulators of Gene Expression, and Identify Novel Anti-tumor Agents

    Published on: August 31, 2013

    Real-time Cytotoxicity Assays in Human Whole Blood
    08:27

    Real-time Cytotoxicity Assays in Human Whole Blood

    Published on: November 7, 2014

    Related Concept Videos

    MALDI-TOF Mass Spectrometry01:19

    MALDI-TOF Mass Spectrometry

    Mass spectrometry is a powerful characterization technique that can identify and separate a wide variety of compounds ranging from chemical to biological entities, based on their mass-to-charge ratio (m/z). The instruments that allow this detection, known as mass spectrometers, have three components: an ion source, a mass analyzer, and a detector. These spectrometers differ based on the nature of their ion source and analyzers.Matrix-assisted laser desorption ionization (MALDI) is a commonly...
    DNA Microarrays02:34

    DNA Microarrays

    Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...

    Articles linked to this work by shared authors, journal, and citation graph.

    Bioengineered miR-148a-3p suppresses glycolysis and amino acid homeostasis in hepatocellular carcinoma cells by regulating multiple solute carrier transporters.

    Liver research (Beijing, China)·2026

    Metabolomics-based predictive biomarker discovery for thiopurine response in Crohn disease: Plasma histidine as a promising biomarker.

    Drug metabolism and disposition: the biological fate of chemicals·2026

    Design, expression, purification, and application of novel recombinant miR-491 molecules to define the biogenesis and function of miR-491-3p versus -5p in posttranscriptional regulation of UDP-glucuronosyltransferase 1A1.

    Drug metabolism and disposition: the biological fate of chemicals·2026

    Efficiency and safety of five different agents for in vivo delivery of novel bioengineered RNAi molecules.

    Frontiers in molecular biosciences·2026

    Comparative effectiveness of 7 major human let-7-5p isoforms to modulate target gene expression in liver cells.

    Drug metabolism and disposition: the biological fate of chemicals·2026

    Small RNA or oligonucleotide drugs and challenges in evaluating drug-drug interactions.

    Frontiers in pharmacology·2025

    Electrochemiluminescence immunoassay for quantifying ZMA001 in human serum: method development, validation, and clinical pharmacokinetic application.

    Bioanalysis·2026

    Highlights from the 17th Japan Bioanalysis Forum Symposium.

    Bioanalysis·2026

    Investigating the relationship between relative accuracy and linearity acceptance criteria in bioassay validation for clinical studies.

    Bioanalysis·2026

    Development of an electrochemiluminescence-based bridging assay to detect antibodies against a PTH inverse agonist in human plasma.

    Bioanalysis·2026

    Advanced assay design for characterizing anti-drug antibody responses in clinical serum samples.

    Bioanalysis·2026

    Development and validation of a LC-MS/MS method for the quantification of the E-type prostanoid receptor 4 antagonist HTL0039732 in human plasma, for a Phase I/IIa clinical trial.

    Bioanalysis·2026

    Detection of antisense oligonucleotides from biological samples by ligase detection reaction using T4 RNA ligase 2.

    BioTechniques·2026

    When left isn't right: A case series of wrong-sided nerve blocks reported to webAIRS.

    Anaesthesia and intensive care·2026

    Detection of prohibited drugs in blood samples using spray mass spectrometry on plasma-treated paper.

    Analytical and bioanalytical chemistry·2026

    CRISPR/Cas12a and CHA-based SERS platform for ultrasensitive nucleic acid detection.

    Analytica chimica acta·2026

    Plasma P-tau217 for detecting amyloid clearance after donanemab in Alzheimer's disease.

    Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

    Making every test count: Insights from a test kit efficiency audit.

    African journal of laboratory medicine·2026
    See all related articles
    JoVE
    x logofacebook logolinkedin logoyoutube logo
    ABOUT JoVE
    OverviewLeadershipBlogJoVE Help Center
    AUTHORS
    Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
    LIBRARIANS
    TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
    RESEARCH
    JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
    EDUCATION
    JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
    Terms & Conditions of Use
    Privacy Policy
    Policies
    Jove
    Visualize
    Contact Us