Titlebook: Bacterial Artificial Chromosomes; Volume 2: Functional Shaying Zhao,Marvin Stodolsky Book 2004 Humana Press 2004

废墟

Simon McGrath,Martin Mulder,Rebecca Suartventional cloning strategies, recombinogenic engineering can be carried out at virtually any chosen position on a given target DNA molecule (which can be small or large). Any type of modification, including sequence deletions, substitutions, and insertions can be carried out via homologous recombina

EVICT

逢迎白雪

https://doi.org/10.1007/978-3-319-08825-9,.). The first successful attempt to perform this technique was carried out by Lin in 1966 (.), who could show that the early fertilized embryo could survive the mechanical damage of inserting a glass needle into the pronucleus. However, it was not until 1981 that small DNA fragments were integrated

感激小女

Handbooks in Health, Work, and Disabilityacterized “single” genes that contribute to a particular trait. However, single-gene expression in transgenic (.) mice is not appropriate for the functional analysis of the many genes that may reside in a typical genetically mapped locus of the order of 1 cM. Bacterial artificial chromosome (BAC) ve

AMEND

Hamidi Abdul Aziz,Salem S. Abu Amroducing a gene of interest into the genome and ectopically expressing it using a heterologous promoter. The choice of the heterologous promoter depends upon the tissue or the time at which a particular gene has to be expressed. Although these transgenic mice have been very informative, quite commonl

即席演说

责任

Jessica A. Deaver,Sudeep C. Popathave been completely sequenced, our knowledge on the function of the majority of herpesvirus genes is still quite insufficient. This is especially true for the members of the β-herpesviruses, i.e., the cytomegaloviruses (CMVs), because their slow replication kinetics, cell association, and large gen

返老还童

蚊帐

András Bárdossy,Abbas El Hachem artificial chromosomes (BACs) and their subsequent transfer into .. Owing to the high frequency of restriction sites, classical cloning methods for site-directed mutagenesis are not applicable to these large viral BACs. One possibility for mutagenesis is allele replacement by a two-step recombinati

critique