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Results for «sgrna»:


Total: 14 results - 0.023 seconds

CRISPR Cas9 sgRNA Design Center 100%

CRISPR Cas9 sgRNA Design Center CRISPR Cas9 sgRNA Design Center CRISPR Cas9 sgRNA Design Center The CRISPR-Cas9 system is a prokaryotic immune system driven by RNA that triggers resistance to foreign genetic elements and provides a form of acquired immunity.

https://www.pdf-archive.com/2018/07/31/crispr-cas9-sgrna-design-center/

31/07/2018 www.pdf-archive.com

Ready-to-use CRISPR Cas9 sgRNA Synthesis 99%

Ready to use CRISPR Cas9 sgRNA Synthesis Ready-to-use CRISPR Cas9 sgRNA Synthesis CRISPR-Cas9 is one of the most convenient types of gene editing technology, and has been widely used in editing genes of many species[1].

https://www.pdf-archive.com/2018/08/01/ready-to-use-crispr-cas9-sgrna-synthesis/

01/08/2018 www.pdf-archive.com

CRISPR Cas9 sgRNA Panel 98%

CRISPR Cas9 sgRNA Panel CRISPR Cas9 sgRNA Panel CRISPR Cas9 sgRNA Panel Due to its simplicity and ease of customization, the CRISPR-Cas9 gene editing system is a popular tool in genetic screening.

https://www.pdf-archive.com/2018/08/01/crispr-cas9-sgrna-panel/

01/08/2018 www.pdf-archive.com

CRISPR Cas9 sgRNA Library Design and Screening 96%

CRISPR Cas9 sgRNA Library Design and Screening CRISPR Cas9 sgRNA Library Design and Screening CRISPR Cas9 sgRNA Library Design and Screening Studying gene functions in metabolic pathway or disease development is very important for disease mechanism research and drug discovery.

https://www.pdf-archive.com/2018/08/01/crispr-cas9-sgrna-library-design-and-screening/

01/08/2018 www.pdf-archive.com

CRISPR Cas9 sgRNA Vector Construction 92%

CRISPR Cas9 sgRNA Vector Construction CRISPR Cas9 sgRNA Vector Construction The CRISPR-Cas9 system is one of the most popular types of gene editing technology, and has been used in increasingly widespread backgrounds over the last few years.

https://www.pdf-archive.com/2018/08/01/crispr-cas9-sgrna-vector-construction/

01/08/2018 www.pdf-archive.com

CRISPR-Cas9 sgRNA Library 86%

CRISPR Cas9 sgRNA Library CRISPR-Cas9 sgRNA Library CRISPR-Cas9 sgRNA Library CRISPR-Cas9/gRNA (CRISPR-Cas RNA-Guided nuclease) is considered as the biggest breakthrough in genome editing technology after TALEN and ZFN.

https://www.pdf-archive.com/2018/08/13/crispr-cas9-sgrna-library/

13/08/2018 www.pdf-archive.com

CRISPR Cas9 85%

The system based on the Cas9 nuclease and an engineered sgRNA that specifies a target nucleic acid sequences.

https://www.pdf-archive.com/2018/07/31/crispr-cas9/

31/07/2018 www.pdf-archive.com

Gene Editing Kits 77%

Creative Biogene’s series products of CRISPR/Cas9 are mainly used for sgRNA vector constructing, sgRNA identification, screening to select the most active sgRNAs and knockout detection.

https://www.pdf-archive.com/2019/07/10/gene-editing-kits/

10/07/2019 www.pdf-archive.com

Abstract 76%

A pooled sgRNA library targeted more than 18,000 protein-coding human genes with multiple sgRNAs.

https://www.pdf-archive.com/2017/06/13/abstract/

13/06/2017 www.pdf-archive.com

Abstract 63%

A pooled sgRNA library targeted more than 18,000 protein-coding human genes with multiple sgRNAs.

https://www.pdf-archive.com/2017/06/14/abstract/

14/06/2017 www.pdf-archive.com

cas9 stable cell line 60%

Compared with ZFNs and TALENs, CRISPR/Cas9 employs sgRNA (single guide RNA) to specify editing which makes the system more precise, time/cost-saving and quite valuable for high-throughput genome editing.

https://www.pdf-archive.com/2019/08/22/cas9-stable-cell-line/

22/08/2019 www.pdf-archive.com

Syno®3.0 Next Generation Gene Synthesis 50%

Contact us Synbio Technologies 1 Deer Park Drive, Suite L-1 Monmouth Junction NJ, 08852 Tel:+1 732-230-3003 Fax:+1 609 228 5911 Web:www.synbio-tech.com E-mail:service@synbio-tech.com  DNA Oligo pools and DNA Oligo pool libraries such as CRISPR-Cas9 sgRNA

https://www.pdf-archive.com/2018/08/13/syno30-next-generation-gene-synthesis/

13/08/2018 www.pdf-archive.com

Genome Editing in Mammalian Cells 49%

Synbio Technologies can provide genome editing in mammalian cells, including CRISPR-Cas9 sgRNA design, synthesis, activity detection, package into lentivirus, transfer into cells and specific gene knock in/out.

https://www.pdf-archive.com/2018/08/03/genome-editing-in-mammalian-cells/

03/08/2018 www.pdf-archive.com

2015 Swiech 47%

Because of the packaging size limitation of AAV vectors5, we designed a dual-vector system that packages SpCas9 (AAV-SpCas9) and sgRNA expression cassettes (AAV-SpGuide) in two separate viral vectors (Fig.

https://www.pdf-archive.com/2015/02/20/2015-swiech/

20/02/2015 www.pdf-archive.com