What are the elements of a cloning vector?
What additional elements does an expression vector contain? What is the purpose of each of these elements?
An origin of replication, a selectable marker, a multiple cloning site, a reporter gene are the elements of a cloning vector.
A promoter, a ribosomal binding site and start codon, a termination codon, a transcription termination sequence, protein tags, elements for transformation like vir genes, integrase are the additional elements that an expression vector contain.
Origin of replication is necessary for the propagation and maintenance of the vector. Selectable marker is necessary for the selection of positively transformed cells. A gene can be conveniently inserted into the vector or removed from it in a multiple cloning site. Reporter genes are used to facilitate the screening of successful clones. A promoter, ribosomal binding site and start codon, termination codon, transcription termination sequence are the elements necessary for the expression of a cloned target gene. Protein tags are necessary to purify the expressed protein. Some expression vectors may contain elements for transformation like the vir genes for plant transformation, and integrase sites for chromosomal insertion.
What are the elements of a cloning vector? What additional elements does an expression vector contain?...
Describe what a cloning vector is and the important features of the vector. What are restriction enzymes and how are they important to molecular biology research? THANKK YOUUU
Question 2,3 and 4
aBbCcDdE AaBbCoDdE Normal No Spacing BamHI 300 EcoRI 3400 1000 2000 5 kb EcoRU Apal List three components a cloning vector must contain A cloning site A replication origin A selectable marker -Drug resistant gene 1. 2. Draw the end of the fragment that will be generated after digestion with the Apal enzyme. Indicate the type of ends generated by this enzyme (Blunt/Sticky, 5' or 3' overhang) (3) 3. What is the size of the plasmid...
A plasmid used as a cloning vector in E. coli must have… Does sequence similarity between genes play an important role in assigning gene function? Successful insertion of a DNA fragment into the multi-cloning region (restriction sites) of a recombinant plasmid is detected by what changes? Understand the concept of (restriction enzyme produced) DNA fragment separation by gel electrophoresis. In addition to restriction enzymes, which enzyme(s) are required to insert a fragment of DNA into a cloning vector? What is...
You are interested in cloning a particular segment of DNA and wish to use a commercial cloning vector with a BamHI cloning site. However, your segment of DNA does not contain the appropriate restriction site. Discussing your problem with a colleague they suggest using PCR to address your problem. How can you use a PCR reaction to facilitate a successful cloning?
3. Below is a diagram of the pUC19 cloning vector (plasmid): Sall EcoRI Hinc Il Kpnl BamHI Accii Pst! Hind III T1 Sacl Xmal xbal BSDMI Sphi Smal Polylinker lacz -ori PUC19 amp Fig_18-08 Genetics, Second Edition 2005 WH Freeman and Company a. Describe briefly the purpose of the: ori: ampR; lacZt: Palxlinker b. When bacteria containing this plasmid are grown on media containing x-gal and ampicillin, why do sometimes you see blue colonies and sometimes white colonies? What does...
Bacterial plasmids often serve as cloning vectors. Describe the essential features of a plasmid vector. What are the advantages and applications of plasmids as cloning vectors?
18. Describe the process of DNA cloning. What do we need? Describe what a vector is. Describe what the vector needs to have to be a good vector. How do you know when it works? Make sure to describe how we make recombinant DNA. I
Which of the following properties is not necessary to make a good plasmid cloning vector? Select one: a. Single recognition site for each restriction endonucleases to be used in cloning b. High copy number c. Selection marker d. Fertility e. Small size
Use the power-reducing formulas to rewrite the expression as an equivalent expression that does not contain powers of trigonometric functions greater than 1. 40 sin ?x cos x 40 sinxcos x = 5-5 cos 4x
Early gene cloning experiments involved insertion at one restriction site in the vector; for example, the insert would have and EcoRI site at each end, and he vector would be opened at an RI site prior to litigation. Under what circumstances would asymmetric cloning be desirable, with the insert having a different site at each end? Please only typed replies and provide source where information was obtained. Thanks