TA Cloning is one of the most popular methods of cloning the amplified PCR product using Taq and other polymerases. These polymerases lack 5'-3' proofreading activity and are capable of adding adenosine triphosphate residue to the 3' ends of the double stranded PCR product. Such PCR amplified product can be cloned in a linearized vector with complementary 3' T overhangs.
TA cloning is brought about by the terminal transferase activity of certain type of DNA polymerase such as the Taq polymerase. This enzyme adds a single, 3'-A overhang to each end of the PCR product. As a result, the PCR product can be directly cloned into a linearized cloning vector that have single base 3'-T overhangs on each end. Such vectors are called T- vectors. The PCR product with A overhang, is mixed with this vector in high proportion. The complementary overhangs of a "T" vector and the PCR product hybridize. The result is a recombinant DNA, the recombination being brought about by DNA ligase.
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.
The insert capacity of a cosmid vector is about 35-45 kb.
Expression vectors contain translation start and termination codons. Moreover, it contains promoter region
Competent cells if i not mistaken
cloning vector
The cloning capacity of pBR322 vector is 1-5kb.
i have no idea wat plasmid,cloning ,and vector means so haha 2 u
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.
The insert capacity of a cosmid vector is about 35-45 kb.
The good cloning vector should have small size, high copy number, own origin of replication, restriction sites for many restriction enzymes and selectable markers.
Expression vectors contain translation start and termination codons. Moreover, it contains promoter region
Competent cells if i not mistaken
No, not really since it is just for cloning. But their should be enough promoter/sequence to provide antibiotic resistance.
there are two types of vectors cloning vector and expression vectors.
We can insert about 5-25 kb sized foreign DNA in a lambda bacteriophage vector.
functions as a vector