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Advanced gene editing
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facet applications:Advanced gene editing
facet content type:Protocol
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Genome Editing in Plants with CRISPR/Cas9
ZFNs and CRISPR/Cas9 advance targeted genome editing, opening new research avenues.
Lentiviral Transduction Protocol
Detailed procedure for how to perform a lentiviral transduction of MISSION shRNA lentiviral particles to achieve a stable long term silencing and phenotypic change.
Ribonucleoprotein (RNP) Protocols Using Synthetic sgRNAs and Cas9 proteins
Combine guaranteed sgRNAs with our comprehensive range of CRISPR products and tools, including Cas9 and delivery reagents, for efficient genome modification with higher specificity.
Universal Transfection Reagent Protocol
Universal Transfection Reagent enables efficient nucleic acid delivery into various cells, compatible with different cell culture conditions.
Lentiviral Production Using X-tremeGENE HP Transfection Reagent
Lentiviruses represent a powerful tool in research applications to transduce a wide range of cell types.
PURedit™ CRISPR Synthetic Guide RNAs and Cas9 Protein
Guaranteed PURedit™ CRISPR synthetic gRNAs and Cas9 protein offer industry-leading on-site cutting and specificity
CRISPR Cas 9 Nuclease RNA-guided Genome Editing
Learn about CRISPR Cas9, what it is and how it works. CRISPR is a new, affordable genome editing tool enabling access to genome editing for all.
使用X-tremeGENE HP转染试剂进行慢病毒生产
慢病毒是一种用于在研究应用中转染多种细胞类型的强大工具。
PURedit™ CRISPR合成引导RNA和Cas9蛋白
可靠的PURedit™ CRISPR合成gRNA和Cas9蛋白可提供行业领先的靶位点切割和特异性
CRISPR / Cas核酸酶RNA介导的基因组编辑
了解CRISPR Cas9、定义和工作原理。CRISPR是一种全新、实惠的基因组编辑工具，可让所有人掌握基因组编辑。
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