λSHK and λAASV: phage vectors for efficient cDNA cloning and expression in mammalian cells

We describe here the construction of two hybrid λ phage vectors for the preparation of directional cDNA libraries that can be used directly, or after their conversion to plasmids, for expression in mammalian cells.

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Veröffentlicht in:Gene 1993-01, Vol.123 (2), p.287-288
Hauptverfasser: Swaroop, Anand, Ganguly, Subinay, Sarkar, Saumyendra N., Vasavada, Haren A.
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container_end_page 288
container_issue 2
container_start_page 287
container_title Gene
container_volume 123
creator Swaroop, Anand
Ganguly, Subinay
Sarkar, Saumyendra N.
Vasavada, Haren A.
description We describe here the construction of two hybrid λ phage vectors for the preparation of directional cDNA libraries that can be used directly, or after their conversion to plasmids, for expression in mammalian cells.
doi_str_mv 10.1016/0378-1119(93)90140-X
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ispartof Gene, 1993-01, Vol.123 (2), p.287-288
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Bacteriophage lambda - genetics
bacteriophage λ
Biological and medical sciences
Biotechnology
Cloning, Molecular - methods
Deoxyribonucleases, Type II Site-Specific
DNA Replication - genetics
Escherichia coli
Fundamental and applied biological sciences. Psychology
Gene Library
Genetic engineering
Genetic technics
Genetic Vectors - genetics
libraries
Mammals
Methods. Procedures. Technologies
phage lambda
Recombinant DNA
Transfection
Vectors (cloning, transfer, expression). Insertion sequences and transposons
title λSHK and λAASV: phage vectors for efficient cDNA cloning and expression in mammalian cells
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