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Biotech Books and Resourses

Below you will find some of the books recommended by the Biotech Learning Institute. If you see a book that you like please add it to your shopping cart.

  1. RNA Interference (RNAi) Nuts and Bolts of RNAi technology, by Dr. David Engelke
  2. DNA Array Image Analysis Nuts and Bolts, by Gerda Kamberova (Editor), Shishir Shah
  3. DNA Microarrays and Gene Expression, by Pierre Baldi (Author), et al
  4. Microarrays Methods and Applications, by Gary Hardiman (Editor)
  5. Microarrays for an Integrative Genomics (Computational Molecular Biology), by I. S. Kohane, et al
  6. Statistical Analysis of Gene Expression Microarray Data, by T. P. Speed (Editor)
  7. A Biologist's Guide to Analysis of DNA Microarray Data, by Steen Knudsen (Author)
  8. Data Analysis Tools for DNA Microarrays, by Sorin Draghici
  9. Microarray Gene Expression Data Analysis, by Helen C. Causton, et al
  10. Bioinformatics for Dummies, by Jean-Michel Claverie (Author), Cedric Notredame (Author)
  11. DNA Microarrays, by David Bowtell (Editor), Joseph Sambrook (Editor)

RNA Interference - Nuts & Bolts of RNAi technology

Price: $44.95
Editor: David Engelke
ISBN: 0966402782

"This book offers protocols and advice for the use of RNA interference for knocking down expression of target genes in a number of different eukaryotes. Varied applications in mammalian systems are explored in depth by authors currently working at the leading edge of RNA Interference methodologies.

Chapters include:
- RNAi in plants
- RNAi in Drosophila
- RNAi in C. elegan
- RNAi in mammalian systems
- RNAi in mice
- Design, synthesis and preparation of synthetic RNAi
- Expression of RNAi from recombinant DNA and viral vectors
- High-throughput applications
- Emerging alternative RNAi methods"


Summary of Chapters

Chapter 1: Targeted gene silencing in plants using RNA interference

The authors of this chapter focus on the design and use of vectors for targeted gene silencing in plants with RNAi. A brief historical perspective of RNAi research in plants is presented with a list of useful references.

Chapter 2: RNAi in Caenorhabditis elegans

In this chapter, the authors discuss the molecular mechanisms, techniques, and applications of RNAi in C. elegans, which was the first multicellular organism to have its genome sequenced. Theoretical considerations and practical approaches are presented in detail.

Chapter 3: Application and analysis of RNAi in Drosophila systems

This chapter describes the application and analysis of RNAi in Drosophila embryo extracts, cultured SL2 cells and in Drosophila embryo development.

Chapter 4: Gene silencing by synthetic siRNA duplexes in mammalian cell culture
This chapter discusses the design and application of synthetic siRNA duplexes for use in mammalian tissue culture. The authors address the advantages of chemically synthesized siRNA duplexes over alternative RNAi protocols. Detailed descriptions of structure, nucleotide composition, target mRNA, and protocol steps are offered..

Chapter 5: Strategies for synthesizing Small Interfering RNA (siRNA)
This chapter provides (1) a complete review of various chemical methods of RNA synthesis; (2) a brief analysis of each of the four alternative siRNA production methods; and (3) a comparative analysis of the relevant utility of all five methods from the perspective of the RNAi practitioner.

Chapter 6: Generating long dsRNA, individual siRNA and siRNA cocktails in vitro

This chapter discusses methods for producing long dsRNA and short interfering RNA using high yield in vitro transcription reactions.

Chapter 7: Optimizing high throughput RNAi-based assays using transient transfection of synthetic siRNAs in cultured mammalian cells

The authors focus on methods for the high throughput characterization of gene functions using siRNAs in mammalian cell cultures, to enable the analysis of a few dozen, hundred or thousand gene targets through a panel of primary screening assays, and to retain the promising ones for more in-depth secondary assays.
Chapter 8: Subcellular delivery and detection of small interfering RNA
Small interfering RNAs (siRNAs) can be expressed in human cells for the down-regulation of specific genes. Localization of the siRNA in the cell is a key factor for success. Expression cassettes, based on several RNApolymerase III promoters, provide a means of synthesizing siRNA hairpins endogenously and the design of the cassettes provides for delivery of the siRNA to different sub cellular locations. Sites of sub cellular localization are determined by in situ hybridization using fluorescently tagged 2'-O-methyl RNA probes. Expression from a U6 snRNA promoter results in nuclear accumulation of the siRNA and reduced target levels. In contrast, promoter cassettes that result in nucleolar and cytoplasmic localization of the siRNA are not effective.

Chapter 9: Downregulation of cellular genes by PCR products expressing siRNAs in Mammalian Cells

Despite the great potential for research application of siRNAs, identifying optimal siRNAs target sites holds some difficulties and it is critical for siRNAs function. One possible way of overcoming this limitation is to have a simple screening procedure that allows the testing of several different sites along a messenger RNA for sensitivity to siRNA. The PCR based method discussed in this chapter has proven to be both facile and robust. The method involves creation of Pol III transcription units by PCR, and direct transfection and testing of these products for siRNA function in cell culture. The chapter discusses protocols and tips in detail.

Chapter 10: Generating Adenoviruses for shRNA or siRNA Delivery

The utility of RNAi as a research tool may be limited by transfection efficiency. Adenovirus vectors efficiently transducer multiple cell types in vitro and in vivo. This chapter serves as a guide to merge the powerful utility of RNAi with the ease of generating and using recombinant adenovirus vectors. Recombinant adenoviruses expressing inhibitory RNAs from constitutive or regulated promoters will find broad applications to studies employing gene silencing.

Chapter 11: Achieving Stable, Heritable Gene Silencing in the Mouse

The authors analyze methods available for creating transgenic models of RNAi in the mouse. Spatial and temporal control of silencing is discussed.

Editor: David Engelke, Ph.D.

David R. Engelke is a Professor of Biological Chemistry and Director of the Program in Biomedical Sciences at the University of Michigan. His laboratory works on the biosynthesis of small RNAs in eukaryotic nuclei, including transcription, localization, and processing mechanisms. His laboratory has contributed to an understanding of how small interfering RNAs can be expressed within human cells. He is the Deputy Editor the journal of the international RNA Society, RNA, and on the editorial board of Nucleic Acids Research.

Cover

Scanning Electron Micrograph of an adult C. elegans male tail. Image by Maureen M. Barr and Renee L. Engle (University of Wisconsin Madison). Photograph was obtained by M.M.B. using a Hitachi S-570 SEM at the E.M. Facility, Building 177B, USDA, Beltsville, MD with the help of Dr. Lynn Carta (USDA) and support of Dr. Paul W. Sternberg (Investigator, Howard Hughes Medical Institute, California Institute of Technology).


DNA Array Image Analysis: Nuts & Bolts

Price: $29.95
Editors: Gerda Kamberova (Editor), Shishir Shah
ISBN:

DNA Array BookBook Info
Text provides a comprehensive introduction to micro array image analysis and includes basic and advanced topics emphasizing aspects of theory and application. Offers practical tips for the novice and advanced user. Expanded-outline format. Softcover.

About the Author
Gerda Kamberova is an assistant professor in computer science at Hofstra University, New York. She teaches computer vision, computer graphics, and artificial intelligence. Shishir Shah is an associate professor at Wayne State University in Detroit, Michigan. Dr. Shah is an author of numerous publications on image analysis and data mining.

Book Description
Common to all DNA and protein array-based technologies is the necessity to analyze digital images of the scanned DNA array. The focus of Kamberova and Shah book is microarray image analysis-from theoretical and application perspective. The topic of microarray image processing is usually neglected due to the availability of various software tools for image processing. The focus of today microarray bioinformatics is data analysis. However, how can one be certain that the data obtained from a microarray experiment through the image analysis is of high quality? How can one perform data mining on data derived from different microarray technologies, where microarray images were analyzed with different image analysis softwares? This book addresses various questions related to microarray image processing.


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