Masoumeh Fallah

Masoumeh Fallah
  • pHD student
  • Shahid Beheshti University

About

4
Publications
642
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12
Citations
Introduction
Current institution
Shahid Beheshti University

Publications

Publications (4)
Article
Full-text available
Introduction Developing somatic embryogenesis is one of the main steps in successful in vitro propagation and gene transformation in the carrot. However, somatic embryogenesis is influenced by different intrinsic (genetics, genotype, and explant) and extrinsic (e.g., plant growth regulators (PGRs), medium composition, and gelling agent) factors whi...
Article
Full-text available
Nisin, derived from Lactococcus lactis, is a well-known natural food preservative. In the present study, the gene of nisin was transformed to carrot by Agrobacterium tumefaciens strain LBA4404 harboring the recombinant binary vector pBI121 containing neomycin phosphotransferase II (nptII) gene, peptide signal KDEL, and Kozak sequence. The integrati...
Article
Full-text available
Background Callus induction is the first step in optimizing plant regeneration. Fit embryogenesis and shooting rely on callus induction. In addition, using artificial intelligence models in combination with an algorithm can be helpful in the optimization of in vitro culture. The present study aimed to evaluate the percentage and speed of callus ind...
Preprint
Full-text available
Plant cell, tissue and organ culture (PCTOC) is extensively used to propagate faster and more plants, to produce virus-free plants, and secondary metabolites production as well. This requires the optimization of PCTOC conditions for each plant and final aim. Optimizing the micropropagation is time-consuming and costly, because it is different from...

Questions

Questions (4)
Question
hi
we have clone desire plasmid enter the DB3 strain, after the extraction plasmid, we see band on Agaros gel, but after digest dont we see any band, where is problem?
thanks?
Question
I underestant my DNA sample contaminante with DNase and no band were found after digest . help me for remove DNase of my DNA sample?
Question
How to make a small piece (20 nt) inside the clone vector?
Question
gRNA design
hello
In the crispor program to find plenty gRNA of desired gene. Selection of indicator between thes?
Thanks

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