A plasmid is a piece of circular DNA. These plasmids are transformed into bacteria/yeast.
A library is made by taking pieces of DNA (from a genomic DNA digest, or cDNA) and inserting them into plasmids. The plasmids are then transformed into the organism and stored. Libraries are used to screen for new functional genes, usually when looking at new substrates or products that the yeast/bacteria can't make without the plasmid.
Due to the fact that the prime [modern day engineered] purpose of plasmids are to transfer Dna, and considering the Rate that we are producing transgenic creatures using plasmids - we have got to go with 'True'.
A helper plasmid is one that allows for the beginning of replication and transfer of other plasmids from a donor to a recipient. Without a helper plasmid, transposons will not be expressed in the recipient.
Recombiant DNA
In the production of a recombinant plasmid, the DNA of interest (insert) and the plasmid vector are both cut with restriction enzymes to create compatible ends. These cut fragments are then ligated together using DNA ligase to produce the recombinant plasmid.
A plasmid is considered recombinant when it contains DNA sequences from two different sources that have been artificially combined, often through genetic engineering techniques like restriction enzyme digestion and ligation. This results in a plasmid with modified or additional genetic material compared to its original form.
A cosmid has the characteristics of a hybrid plasmid. They are used in the building of genomic libraries. They are ~200 base pairs long. More detailed information is available on Wikipedia.
Due to the fact that the prime [modern day engineered] purpose of plasmids are to transfer Dna, and considering the Rate that we are producing transgenic creatures using plasmids - we have got to go with 'True'.
R-plasmid
TOL plasmid
BAC = Bacterial Artificial Chromosome -200-300Kb -good for genomic libraries -uses the bacterial F (sex) plasmid -currently quite popular YAC = Yeast Artificial Chromosome -1Mb -good for genomic libraries also -difficult to manipulate and use -less popular
You can determine if your bacteria contain a plasmid by performing a plasmid extraction followed by gel electrophoresis to visualize the presence of plasmid DNA. Other methods include PCR amplification of plasmid-specific sequences or using molecular biology techniques like restriction enzyme digestion to confirm the presence of a plasmid.
A plasmid which encodes genes for its own transfer.
Plasmid is extrachromosomal DNA capable of self replication.
A helper plasmid is one that allows for the beginning of replication and transfer of other plasmids from a donor to a recipient. Without a helper plasmid, transposons will not be expressed in the recipient.
You can have a maximum of 8 plasmid slots.
Recombiant DNA
The plasmid is found in prokaryotic cells.