Object structure
Title:

Artificially engineered specific nucleases - a breakthrough in RE research - Rewiev

Subtitle:

Artificially engineered specific nucleases - a breakthrough in RE research - Rewiev

Creator:

Cesnaviciene, Egle

Publisher:

Committee on Biotechnology PAS ; Institute of Bioorganic Chemistry PAS

Date issued/created:

2003

Description:

artykuł promocyjny

Subject and Keywords:

biotechnology

Abstract:

During the last few decades, several hundred type II restriction enzymes have been isolated and characterized from variousbacterial strains, and yet, many specificities are still unavailable.There is an increasing demand for a wider selection of restriction enzymes with varying recognition sequences, which hasstimulated efforts to produce artificial restriction enzymes. Therapidly expanding field of protein engineering couples studies ofprotein structure and function with molecular evolution basedon random mutagenesis and high throughput screening to create enzymes having desired properties.

Relation:

Biotechnologia, vol.61, 2 (2003)-.

Volume:

61

Issue:

2

Start page:

7

End page:

11

Resource type:

Text

Detailed Resource Type:

Article

Format:

application/pdf

Resource Identifier:

0860-7796 ; IChB B-57

Source:

Library of Institute of Bioorganic Chemistry PAS

Language:

eng

Language of abstract:

eng

Temporal coverage:

1988-2010

Rights:

Creative Commons Attribution BY-SA 4.0 license

Terms of use:

Copyright-protected material. [CC BY-SA 4.0] May be used within the scope specified in Creative Commons Attribution BY-SA 4.0 license, full text available at:

Digitizing institution:

Institute of Bioorganic Chemistry of the Polish Academy of Science

Original in:

Institute of Bioorganic Chemistry of the Polish Academy of Science

Projects co-financed by:

Operational Program Digital Poland, 2014-2020, Measure 2.3: Digital accessibility and usefulness of public sector information; funds from the European Regional Development Fund and national co-financing from the state budget.

Access:

Open

×

Citation

Citation style: