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Description : This image shows a line drawing of a bacterium with its chromosomal DNA and several plasmids within it. The bacterium is drawn as a large oval. Within the bacterium, small to medium size circles illustrate the plasmids, and one long thin closed line that intersects itself repeatedly illustrates the chromosomal DNA.
This image is a derivative work of the following images: Example plasmid.png licensed with Cc-by-sa-3.0-migrated, GFDL 2006-05-09T14:32:22Z Magnus Manske 248x242 (1921 Bytes) {{Information| |Description= Description : This image shows a line drawing of a plasmid. The plasmid is drawn as two concentric circles that are very close together, with ...
Description : This image shows a line drawing that compares the activity of non-integrating plasmids, on the top, with episomes, on the bottom, during cell division. The upper half of the image shows a bacterium with its chromosomal DNA and plasmids dividing into two identical bacteria, each with their chromosomal DNA and plasmids.
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Various Azospirillum species possess seven replicons; A. lipoferum, for instance, has one bacterial chromosome, five chromids, and one plasmid. [4] Plasmids and bacteriophages are usually replicated as single replicons, but large plasmids in Gram-negative bacteria have been shown to carry several replicons.
Vector map of pUC19. pUC19 is one of a series of plasmid cloning vectors designed by Joachim Messing and co-workers. [1] The designation "pUC" is derived from the classical "p" prefix (denoting "plasmid") and the abbreviation for the University of California, where early work on the plasmid series had been conducted. [2]
ColE1 is a plasmid found in bacteria. Its name derives from the fact that it carries a gene for colicin E1 (the cea gene). It also codes for immunity from this product with the imm gene. In addition, the plasmid has a series of mobility (mob) genes.
production of a 'parental plasmid' (bacterial plasmid with eukaryotic inserts) in E. coli; induction of a site-specific recombinase at the end of this process but still in bacteria. These steps are followed by the excision of prokaryotic vector parts via two recombinase-target sequences at both ends of the insert
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