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Schizosaccharomyces pombe

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Cover of 'Schizosaccharomyces pombe'

Table of Contents

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    Book Overview
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    Chapter 1 Preparation of Solutions and Reagents
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    Chapter 2 Analysis of Fission Yeast Single DNA Molecules on the Megabase Scale Using DNA Combing
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    Chapter 3 Chromatin Immunoprecipitation-Polymerase Chain Reaction (ChIP-PCR) Detects Methylation, Acetylation, and Ubiquitylation in S. pombe
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    Chapter 4 Primer Design and Inverse PCR on Yeast Display Antibody Selection Outputs
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    Chapter 5 Molecular Cloning and Characterization of Small Viral Genome in Fission Yeast
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    Chapter 6 Total RNA Isolation and Quantification of Specific RNAs in Fission Yeast
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    Chapter 7 Analysis of Reverse Transcribed mRNA Using PCR and Polyacrylamide Gel Electrophoresis
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    Chapter 8 The No-Nonsens SDS-PAGE
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    Chapter 9 Crystallization of Recombinant α-Actinin and Related Proteins
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    Chapter 10 Estimation of GFP-Nucleoporin Amount Based on Fluorescence Microscopy
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    Chapter 11 Antibody Pull-Down Experiments in Fission Yeast
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    Chapter 12 Preparation of Cell Lysates of Fission Yeast for Immunoprecipitation
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    Chapter 13 Wide-band Electrical Impedance Spectroscopy (EIS) Measures S. pombe Cell Growth in vivo
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    Chapter 14 In Situ Chromatin-Binding Assay Using Epifluorescent Microscopy in S. pombe
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    Chapter 15 High-Frequency Lithium Acetate Transformation of Schizosaccharomyces pombe
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    Chapter 16 Tetrad Dissection in Fission Yeast
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    Chapter 17 Random Spore Analysis in Fission Yeast
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    Chapter 18 Duplication and Transformation of the Schizosaccharomyces pombe Collection of Deletion Strains
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    Chapter 19 Schizosaccharomyces pombe Biotechnological Applications in Winemaking
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    Chapter 20 Schizosaccharomyces pombe Isolation Protocol
Attention for Chapter 7: Analysis of Reverse Transcribed mRNA Using PCR and Polyacrylamide Gel Electrophoresis
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Chapter title
Analysis of Reverse Transcribed mRNA Using PCR and Polyacrylamide Gel Electrophoresis
Chapter number 7
Book title
Schizosaccharomyces pombe
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7546-4_7
Pubmed ID
Book ISBNs
978-1-4939-7545-7, 978-1-4939-7546-4
Authors

Pranjal Biswas, Uddalak Majumdar, Sanjay Ghosh, Biswas, Pranjal, Majumdar, Uddalak, Ghosh, Sanjay

Abstract

The patterns of gene expression in the fission yeast Schizosaccharomyces pombe under various experimental conditions form the basis of any transcriptomic study. We describe a method involving reverse transcription of the mRNA, Polymerase Chain Reaction (PCR), and the subsequent separation of the products onto Urea-Polyacrylamide gel that can be used to study the gene expression patterns in the fission yeast. The method described is cost effective and reproducible with satisfactory resolution of expressed transcripts in the gel. The method has the following essential steps: total RNA isolation and purification, cDNA synthesis from mRNAs, PCR amplification of cDNAs, visualization of PCR products, re-amplification and cloning of the differentially expressed PCR products, sequencing the confirmed clones, and finally cDNA library screening to isolate the genes of interest. The technique is also popularly known as Differential Display Reverse Transcription (DDRT-PCR). After its invention in 1992, a number of modifications have been introduced to optimize the technique and specifically to reduce the major problem of "false positives." Since understanding of specific gene expression patterns that regulate developmental and stress responses is a major concern of biology, DDRT-PCR has become a very popular molecular technique during the past two decades.

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Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 40%
Professor 1 20%
Researcher 1 20%
Student > Bachelor 1 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 40%
Veterinary Science and Veterinary Medicine 1 20%
Medicine and Dentistry 1 20%
Engineering 1 20%