You need JavaScript to view this

DNA cloning: a practical approach. Volume 1

Abstract

This book is written for the advanced molecular biologist who needs a detailed discussion of cloning technology. Topics of discussion include: genomic library cloning (size of a genomic library, screening methods, chromosome walking, host cell genetics, and general features of bacteriophage Iambda); use of gt10 and gt11 cDNA lambda vectors and general cDNA cloning; RNase H-Pol I cDNA synthesis; method of detecting fusion proteins produced in bacteria; pEMBL family of double-stranded plasmid vectors that can be used to generate single strands; Escherichia coli transformation; production of mutations in cloned sequences; and cloning in gram negative bacteria.
Authors:
Glover, D M [1] 
  1. ed.
Publication Date:
Jan 01, 1985
Product Type:
Book
Reference Number:
EDB-87-172190
Resource Relation:
Other Information: From review in BioScience, Vol. 37, No. 4 (1987)
Subject:
59 BASIC BIOLOGICAL SCIENCES; DNA-CLONING; MOLECULAR BIOLOGY; BACTERIOPHAGES; DNA REPLICATION; DNA SEQUENCING; ESCHERICHIA COLI; MUTATIONS; PROTEINS; BACTERIA; CLONING; MICROORGANISMS; NUCLEIC ACID REPLICATION; ORGANIC COMPOUNDS; PARASITES; STRUCTURAL CHEMICAL ANALYSIS; VIRUSES; 550200* - Biochemistry
OSTI ID:
5905779
Country of Origin:
United Kingdom
Language:
English
Submitting Site:
JMT
Size:
Pages: 190
Announcement Date:

Citation Formats

Glover, D M. DNA cloning: a practical approach. Volume 1. United Kingdom: N. p., 1985. Web.
Glover, D M. DNA cloning: a practical approach. Volume 1. United Kingdom.
Glover, D M. 1985. "DNA cloning: a practical approach. Volume 1." United Kingdom.
@misc{etde_5905779,
title = {DNA cloning: a practical approach. Volume 1}
author = {Glover, D M}
abstractNote = {This book is written for the advanced molecular biologist who needs a detailed discussion of cloning technology. Topics of discussion include: genomic library cloning (size of a genomic library, screening methods, chromosome walking, host cell genetics, and general features of bacteriophage Iambda); use of gt10 and gt11 cDNA lambda vectors and general cDNA cloning; RNase H-Pol I cDNA synthesis; method of detecting fusion proteins produced in bacteria; pEMBL family of double-stranded plasmid vectors that can be used to generate single strands; Escherichia coli transformation; production of mutations in cloned sequences; and cloning in gram negative bacteria.}
place = {United Kingdom}
year = {1985}
month = {Jan}
}