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High Capacity Vectors
Since the construction of the first generation of general cloning vectors in the early 1970s, a large number of cloning vectors have been developed. Despite the bewildering choice of commercial and other available vectors, the selection of cloning vector to be used can be decided by applying a small...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120981/ http://dx.doi.org/10.1007/978-81-322-1554-7_1 |
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author | Bajpai, Bhakti |
author_facet | Bajpai, Bhakti |
author_sort | Bajpai, Bhakti |
collection | PubMed |
description | Since the construction of the first generation of general cloning vectors in the early 1970s, a large number of cloning vectors have been developed. Despite the bewildering choice of commercial and other available vectors, the selection of cloning vector to be used can be decided by applying a small number of criteria: insert size, copy number, incompatibility, selectable marker cloning sites, and specialized vector functions. Several of these criteria are dependent on each other. Most general cloning plasmids can carry a DNA insert up to around 15 kb in size. Several types of vectors are available for cloning large fragments of DNA too. This chapter presents a consolidated account of some new generation of high-capacity vectors such as cosmid, yeast artificial chromosome (YAC) , bacterial artificial chromosome (BAC), P1 phage artificial chromosome (PAC), and human artificial chromosome (HAC). |
format | Online Article Text |
id | pubmed-7120981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71209812020-04-06 High Capacity Vectors Bajpai, Bhakti Advances in Biotechnology Article Since the construction of the first generation of general cloning vectors in the early 1970s, a large number of cloning vectors have been developed. Despite the bewildering choice of commercial and other available vectors, the selection of cloning vector to be used can be decided by applying a small number of criteria: insert size, copy number, incompatibility, selectable marker cloning sites, and specialized vector functions. Several of these criteria are dependent on each other. Most general cloning plasmids can carry a DNA insert up to around 15 kb in size. Several types of vectors are available for cloning large fragments of DNA too. This chapter presents a consolidated account of some new generation of high-capacity vectors such as cosmid, yeast artificial chromosome (YAC) , bacterial artificial chromosome (BAC), P1 phage artificial chromosome (PAC), and human artificial chromosome (HAC). 2013-10-22 /pmc/articles/PMC7120981/ http://dx.doi.org/10.1007/978-81-322-1554-7_1 Text en © Springer India 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Bajpai, Bhakti High Capacity Vectors |
title | High Capacity Vectors |
title_full | High Capacity Vectors |
title_fullStr | High Capacity Vectors |
title_full_unstemmed | High Capacity Vectors |
title_short | High Capacity Vectors |
title_sort | high capacity vectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120981/ http://dx.doi.org/10.1007/978-81-322-1554-7_1 |
work_keys_str_mv | AT bajpaibhakti highcapacityvectors |