Molecular toxicology protocols /

Bibliographic Details
Other Authors: Keohavong, Phouthone, Grant, Stephen G.
Format: Book
Language:English
Published: Totowa, N.J. : Humana Press, [2005]
Series:Methods in molecular biology (Clifton, N.J.) ; v. 291.
Subjects:
Table of Contents:
  • ³²P-postlabeling analysis of DNA adducts
  • Modification of the ³²P-postlabeling method to detect a single adduct species as a single spot
  • DNA isolation and sample preparation for quantification of adduct levels by accelerator mass spectrometry
  • Fluoroimaging-based immunoassay of DNA photoproducts in ultraviolet-B-irradiated tadpoles
  • Analysis of DNA strand cleavage at abasic sites
  • Premature chromosome condensation in human resting peripheral blood lymphocytes for chromosome aberration analysis using specific whole-chromosome DNA hybridization probes
  • Mutagen-induced chromatid breakage as a marker of cancer risk
  • Flow cytometric analysis of micronuclei in erythrocytes
  • The comet assay : a sensitive genotoxicity test for the detection of DNA damage
  • Computerized image analysis software for the comet assay
  • The comet-FISH technique : a tool for detection of specific DNA damage and repair
  • DNA double-strand break damage and repair assessed by pulsed-field gel electrophoresis
  • Analysis of in vivo mutation in the Hprt and Tk genes of mouse lymphocytes
  • Quantifying in vivo somatic mutations using transgenic mouse model systems
  • Methods for detecting somatic mutations in vitro : the human T-cell cloning assay selecting for HPRT mutants
  • Molecular analysis of mutations in the human HPRT gene
  • Simultaneous quantification of t (14;18) and HPRT Exon 2/3 deletions in human lymphocytes
  • The GPA in vivo somatic mutation assay
  • Flow cytometric measurement of mutant T cells with altered expression of TCR : detecting somatic mutations in humans and mice
  • Mutation screening of the TP53 gene by temporal temperature gradient gel electrophoresis
  • Analysis of K-RAS and P53 mutations in sputum samples
  • Allele-specific competitive blocker-PCR detection of rare base substitution
  • Gel-based nonradioactive single-strand conformational polymorphism and mutation detection : limitations and solutions
  • Detection and characterization of oncogene mutations in preneoplastic and early neoplastic lesions
  • Detection of DNA double-strand breaks and chromosome translocations using ligation-mediated PCR and inverse PCR
  • Microsatellite instability : an indirect assay to detect defects in the cellular mismatch repair machinery
  • Unscheduled DNA synthesis : a functional assay for global genomic nucleotide excision repair
  • Analysis of DNA repair using transfection-based host cell reactivation
  • An immunoassay for measuring repair of ultraviolet photoproducts
  • Analysis of DNA double-strand break repair by nonhomologous end joining in cell-free extracts from mammalian cells
  • Measuring recombination proficiency in mouse embryonic stem cells
  • Strategies for measurement of biotransformation enzyme gene expression
  • Genotyping technologies : application to biotransformation enzyme genetic polymorphism screening
  • TaqMan flurogenic detection system to analyze gene transcription in autopsy material
  • Development of quantitative reverse transcriptase PCR assays for measuring gene expression
  • Quantification of selective phosphatidylserine oxidation during apoptosis
  • Quantitative method of measuring phophatidylserine externalization during apoptosis using electron paramagnetic resonance spectroscopy and annexin-conjugated iron
  • Detection of programmed cell death in cells exposed to genotoxic agents using a caspase activation assay