Molecular Evolution, Producing the Biochemical Data, Part B, Parte 2Elsevier, 15 jun 2005 - 896 páginas The critically acclaimed laboratory standard, Methods in Enzymology, is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. The series contains much material still relevant today - truly an essential publication for researchers in all fields of life sciences. Molecular Evolution Producing the Biochemical Data part B is a continuation of methods published in Part A (1993, volume 224). The work is a very methodological look at markers, templates, genomes, datasets and analyses used in studies of biological diversity. * One of the most highly respected publications in the field of biochemistry since 1955 * Frequently consulted, and praised by researchers and reviewers alike * Truly an essential publication for anyone in any field of the life sciences |
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Molecular Evolution, Producing the Biochemical Data Elizabeth A. Zimmer No hay ninguna vista previa disponible - 2005 |
Términos y frases comunes
AFLP alignment alleles amino acid amplification analysis analyze approach Arabidopsis assay bacteria bands Biol biological buffer cDNA cells Centrifuge chloroplast chloroplast genome chromosomes clones confocal containing coverslip database datasets detection digestion DNA extraction DNA microarrays DNA sequences Ecol Edited EDTA electrophoresis enzyme estimated ethanol Evol evolution evolutionary filter fluorescent fragments functional gene duplication gene expression genetic diversity genome sequences genomic DNA genotyping hybridization identify Incubate inferred isolation labeled ligation loci markers methods microarray Microbiol microsatellite mitochondrial molecular mRNA mtDNA Nucleic Acids nucleotide oligonucleotide optimal organisms orthologous paralogs PCR products pellet phylogenetic phylogeny plant plasmid polymerase polymerase chain reaction polymorphism population primer pairs probes protein protocol reaction reconstruction regions restriction restriction enzyme rRNA samples selection slide solution species staining step structure studies supernatant supertree techniques temperature tion tissue transformation tree tube Volume
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