๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Evaluation of the tetracycline promoter system for regulated gene expression in Kluyveromyces marxianus

โœ Scribed by Douglas C. Pecota; Nancy A. Da Silva


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
172 KB
Volume
92
Category
Article
ISSN
0006-3592

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Evaluation of the tetracycline-repressib
โœ Gschwend, Jรผrgen E.; Fair, William R.; Powell, C. Thomas ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 330 KB ๐Ÿ‘ 2 views

## BACKGROUND. Studies of genes that may inhibit growth or induce death of cells are facilitated greatly by tightly controlled expression of those genes. A promising system for control of transgene expression over a wide range is the tetracycline-repressible transactivator (tTA) system developed b

A Set of Vectors with a Tetracycline-Reg
โœ Garรญ, Eloi; Piedrafita, Lidia; Aldea, Martรญ; Herrero, Enrique ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 158 KB ๐Ÿ‘ 2 views

A set of Saccharomyces cerevisiae expression vectors has been developed in which transcription is driven by a hybrid tetO-CYC1 promoter through the action of a tetR-VP16 (tTA) activator. Expression from the promoter is regulated by tetracycline or derivatives. Various modalities of promoter and acti

On the use of the T-RExโ„ข tetracycline-in
โœ Vasily N. Dobrovolsky; Robert H. Heflich ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 223 KB ๐Ÿ‘ 1 views

## Abstract Components of the commercially available Tโ€RExโ„ข system were used to create two types of transgenic mice. The first contained the tetracyclineโ€repressor transgene under the control of the CMV promoter/enhancer; the second type contained a green fluorescent protein (GFP) reporter transgen

Functional analysis of yeast essential g
โœ Bellรญ, Gemma; Garรญ, Eloi; Aldea, Martรญ; Herrero, Enrique ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 339 KB ๐Ÿ‘ 2 views

A promoter-substitution cassette has been constructed that allows one-step substitution of chromosomal gene promoters for the tetracycline-regulatable tetO promoter in yeast cells, which uses kanMX4 as selective marker for geneticin resistance. Oligonucleotides for PCR amplification of the cassette