- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1472-6750
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Design and cloning strategies for constructing shRNA expression vectors ; volume:6 ; number:1 ; day:05 ; month:1 ; year:2006 ; pages:1-8 ; date:12.2006
BMC biotechnology ; 6, Heft 1 (05.1.2006), 1-8, 12.2006
- Creator
-
Mcintyre, Glen J.
- Contributor
-
Fanning, Gregory C.
SpringerLink (Online service)
- DOI
-
10.1186/1472-6750-6-1
- URN
-
urn:nbn:de:1111-2016072531796
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:44 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mcintyre, Glen J.
- Fanning, Gregory C.
- SpringerLink (Online service)
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A novel cloning strategy for one-step assembly of multiplex CRISPR vectors
Development of a novel method for rapid cloning of shRNA vectors, which successfully knocked down CD44 in mesenchymal triple-negative breast cancer cells
Altering the selection capabilities of common cloning vectors via restriction enzyme mediated gene disruption
Criteria for effective design, construction, and gene knockdown by shRNA vectors
Strategies for Constructing and Operating DNA Origami Linear Actuators
A new method to customize protein expression vectors for fast, efficient and background free parallel cloning
Protocol: Streamline cloning of genes into binary vectors in Agrobacterium via the Gateway® TOPO vector system
Automated seamless DNA co-transformation cloning with direct expression vectors applying positive or negative insert selection
New destination vectors facilitate Modular Cloning for Chlamydomonas
New destination vectors facilitate Modular Cloning for Chlamydomonas
Cloning vectors derived from plasmids and phage of Bacillus
A novel series of high-efficiency vectors for TA cloning and blunt-end cloning of PCR products
A novel cloning strategy for one-step assembly of multiplex CRISPR vectors
Development of a novel method for rapid cloning of shRNA vectors, which successfully knocked down CD44 in mesenchymal triple-negative breast cancer cells
Altering the selection capabilities of common cloning vectors via restriction enzyme mediated gene disruption
Criteria for effective design, construction, and gene knockdown by shRNA vectors
Strategies for Constructing and Operating DNA Origami Linear Actuators
A new method to customize protein expression vectors for fast, efficient and background free parallel cloning
Protocol: Streamline cloning of genes into binary vectors in Agrobacterium via the Gateway® TOPO vector system