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OLS Field Name OLS Field Data
Main Title PCR applications : protocols for functional genomics /
Other Authors
Author Title of a Work
Sninsky, John J.
Innis, Michael A.
Gelfand, David H.
Publisher Academic Press,
Year Published 1999
OCLC Number 41339460
ISBN 0123721857; 9780123721853; 0123721865; 9780123721860
Subjects Polymerase chain reaction. ; Gene amplification. ; Polymerase chain reaction--Laboratory manuals. ; Gene amplification--Laboratory manuals. ; Genomics--Laboratory manuals. ; Polymerase Chain Reaction--methods. ; Genetic Engineering. ; Polymerase kettingreactie. ; Genoom. ; Methode.--(DE-588)4038971-6 ; Polymerase-Kettenreaktion.--(DE-588)4256726-9 ; Amplification génique. ; Réaction en chaãine de la polymérase--Manuels de laboratoire. ; Aufsatzsammlung. ; Polymerase Chain Reaction--methods--laboratory manuals ; Genetic Engineering--laboratory manuals ; Genomes ; Polymerase chain reaction--Diagnostic use
Internet Access
Description Access URL
Table of contents http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=008603374&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
Table of contents http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008603374&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
Publisher description http://catdir.loc.gov/catdir/description/els033/99211203.html
https://www.sciencedirect.com/science/book/9780123721853
Holdings
Library Call Number Additional Info Location Last
Modified
Checkout
Status
EKCR  QP606.D46P346 1999 NHEERL/GED Library/Gulf Breeze,FL 09/24/1999
Collation xviii, 566 pages, [3] pages of plates : illustrations (some color) ; 24 cm
Notes
Includes bibliographical references and index.
Contents Notes
pt. 1. Key concepts for PCR-- Ch. 1. Optimization of PCR: conversations between Michael and David-- Ch. 2. The convergence of PCR, computers, and the human genome project: past, present, and future-- Ch. 3. Thermostable DNA polymerases: an update-- Ch. 4. Musings on microbial genomes-- Ch. 5. Statistical refinement of primer design parameters-- Ch. 6. Multiplex PCR: optimization guidelines-- Ch. 7. The use of immobilized mismatch binding protein for the optimization of PCR fidelity. Ch. 8. A new generation of PCR instruments and nucleic acid concentration systems-- Ch. 9. Sequencing PCR products-- Ch. 10. Recent advances in high-temperature reverse transcription and PCR-- Ch. 11. Viral genotyping by a quantitative point mutation assay: application to HIV-1 drug resistance-- Ch. 12. In situ PCR-- pt. 2. Quantitative PCR-- Ch. 13. Standards for PCR assays-- Ch. 14. Rapid thermal cycling and PCR kinetics-- Ch. 15. Kinetics of competitive reverse transcriptase-PCR. Ch. 16. Kinetic PCR analysis using a CCD camera and without using oligonucleotide probes-- Ch. 17. Quantification of telomerase activity using telomeric repeat amplification protocol-- pt. 3. Gene discovery-- Ch. 18. Differential display-- Ch. 19. Single-cell cDNA libraries-- Ch. 20. Whole cell assays-- Ch. 21. Screening differentially displayed PCR products by single-strand conformation polymorphism gels-- Ch. 22. Microsatellite protocols-- Ch. 23. Real-time quantitative PCR: uses in discovery research. Ch. 24. Homology cloning: a molecular taxonomy of the archaea-- Ch. 25. Cloning mammalian homologs of drosophila genes-- Ch. 26. Cloning human homologs of yeast genes-- pt. 4. Genomics and expression profiling-- Ch. 27. Cellular transcriptome analysis using a kinetic PCR assay-- Ch. 28. Parallel analysis with biological chips-- Ch. 29. High-density cDNA grids for hybridization fingerprinting experiments-- Ch. 30. Comparative genomics hybridization-- Ch. 31. Genetic footprinting and functional maps of the yeast genome. Ch. 32. Molecular analysis of microdissected tissue: laser capture microdissection-- Ch. 33. Amplified fragmant length polymorphism: studies on plant development-- Ch. 34. A florescent, multiplex solid-phase minisequencing method for genotyping cytochrome P450 genes-- Ch. 35. The Cleavase I enzyme for mutation and polymorphism scanning.