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pTV118N phagemid vector

For research use only. Not intended for any clinical use.
Cat.No.
VPT4036
Description
pTV118N is a phagemid vector constructed from a modified pUC118. This plasmid contains the sequence CCATGG which includes the cleavage sequence for the restriction enzyme NcoI as well as the start codon (ATG) for lacZ. This enables target gene expression at the NcoI site. Protein expression is enabled by the vector's lac promoter. The pTV118N vector also contains a lacZ SD sequence. There are eight bases between the lacZ SD sequence and the initiation codon, allowing high level expression of target genes. Induction of single-stranded DNA by helper phage and its subsequent sequencing with RV-N primer enables accurate sequencing from the start codon site, ensuring an insert's correct translation frame.
Vector Length
3,163 bp
Vector Type
phagemid vector
Vector Map

Background

Applications

Publications

Q & A

Customer Reviews

The pTV118N is a hybrid phagemid vector that is constructed from the modified pUC118 plasmid. This specialized vector is distinguished by the presence of a CCATGG sequence, which serves dual functions. Firstly, it incorporates the cleavage site for the NcoI restriction enzyme, enabling targeted dissection of genetic material at this specific site. Secondly, the sequence encompasses the start codon ATG for the lacZ gene that permits commencement of specific gene expression. Altogether, this facilitates the specific expression of any target gene at the NcoI site. Notable, the pTV118N vector operates through the lac promoter system, which is incorporated into its design. This lac promoter system plays a pivotal role in enabling efficient protein expression. Furthermore, this vector includes a lacZ Shine-Dalgarno (SD) sequence. The lacZ SD sequence is positioned eight bases from the initiation codon, creating an optimal context for the high-level expression of target genes. Another key feature of the pTV118N vector that contributes to its utility is the mechanism for the induction of single-stranded DNA by a helper phage. This innovative approach allows the accurate sequencing of the start codon site. The inclusion of the RV-N primer ensures precise sequencing by starting it from the start codon site. This capability secures the correct translation frame of an insert. This ability to determine the exact nucleotide sequence of DNA fragments from the start codon site enhances the accuracy and efficacy of genetic engineering applications.
The pTV118N phagemid vector is a versatile tool used in various areas of genetic and molecular biology research. Here are its applications: Recombinant Protein Production: pTV118N is commonly used for producing recombinant proteins in bacterial cells. Its high copy number ensures high yields of the protein of interest. Cloning: This vector is used for cloning of genes, sections of DNA, or whole genomes for analysis and experimentation. It offers ease of insertion and extraction of the genetic sequences of interest. Study of Gene Function: The vector aids in the study of gene functions including the production of recombinant proteins and observation of phenotypic changes in transformed organisms. Phage Display: Since pTV118N is a phagemid, it can be used in phage display technologies – a method where a gene encoding a protein or peptide is expressed as a fusion with a coat protein on the surface of a bacteriophage. Biochemical and Structural Studies: pTV118N allows for the large-scale expression and purification of proteins for subsequent biochemical and structural characterization. Vaccine Development: It can be used to express potential antigenic proteins, which can then be used in the production of vaccines.
Customer Q&As
What is the difference between phagemid and plasmid?

A: Unlike commonly used plasmids, phagemid vectors are distinguished by their ability to be packaged into the capsid of a bacteriophage because they possess a genetic sequence that emits a packaging signal.

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Customer Reviews
High success rate

Ease of use and high success rate are two features that significantly stand out for the Creative Biogene's pTV118N phagemid vector. Its significant role in simplifying the process of single stranded DNA production is much appreciated. I highly recommend it to peers and colleagues for their research work.

Canada

01/20/2020

Good transformation efficiency

I have tried several phagemid vectors for my cloning experiments, and the pTV118N stands out as one of the most reliable ones. This vector has consistently provided good transformation efficiency.

Canada

12/05/2023

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