The insert capacity of a cosmid vector is about 35-45 kb.
"Vector" is an agent that can carry a DNA fragment into a host cell. If it is used for reproducing the DNA fragment, it is called a "cloning vector". If it is used for expressing certain gene in the DNA fragment, it is called an "expression vector".Commonly used vectors include plasmid, Lambda phage, cosmid and yeast artificial chromosome (YAC).
In a M13 phage we can insert about 1-4 kb of target DNA sequence which is its maximum insert capacity.
plasmid is the type of the cloning vector. other cloning vectors includes cosmids, bacteriophage, phagemids, artifiical chromosomes. clonong vectors are the carriers of certain traits to be inserted in non coding regions of the DNA.
Expression vectors contain translation start and termination codons. Moreover, it contains promoter region
Competent cells if i not mistaken
We can insert about 5-25 kb sized foreign DNA in a lambda bacteriophage vector.
The cloning capacity of pBR322 vector is 1-5kb.
You can add maximum 70-100 kb of genetic material in a P1 phage vector.
it is a ds DNA use in recombinant DNA technology to insert our interested gene and multiply it.Ex;plasmid,cosmid
"Vector" is an agent that can carry a DNA fragment into a host cell. If it is used for reproducing the DNA fragment, it is called a "cloning vector". If it is used for expressing certain gene in the DNA fragment, it is called an "expression vector".Commonly used vectors include plasmid, Lambda phage, cosmid and yeast artificial chromosome (YAC).
i have no idea wat plasmid,cloning ,and vector means so haha 2 u
The first step is restriction of the cosmid and the foreign DNA with the restriction enzyme, then ligating the fragments together. Thereafter, the cosmids are loaded into the phage capsid, which leads to the expression of the foreign gene through transduction.
In a M13 phage we can insert about 1-4 kb of target DNA sequence which is its maximum insert capacity.
plasmid is the type of the cloning vector. other cloning vectors includes cosmids, bacteriophage, phagemids, artifiical chromosomes. clonong vectors are the carriers of certain traits to be inserted in non coding regions of the DNA.
Gene Cloning is used to clone a gene of interest in a vector called plasmid. The chimeric DNA or rDNA formed by cloning is stable and can be used to propagate and sequence the DNA. producing vector containing inulin gene is an example.
Vector
You can identify the ligated DNA insert into a vector by doing DNA double digestion. Let say you inserted your foreign DNA with restriction sites Sma I and EcoRI. After ligation, you can digest the amplified chimeric rDNA with the same restriction enzyme. You can find the vector and the foreign insert on the resolved gel clearly if your cloning and digestion work properly.You can also confirm this by DNA sequencing.