Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CC-18
| Cat. No. | CC-18 |
| Description | All-in-one, ready-to-use SaCas9 and guide RNA (gRNA) expression plasmids for use with dicots, especially with Arabidopsis. The Dicots SaCas9 Genome Editing Kit is a highly effective and accurate gene editing kit which is based on the latest artificial endonuclease CRISPR/SaCas9. |
| Efficiency | SaCas9 expression cassette and sgRNA expression cassette are combined into one vector which offers a higher transformation efficiency. |
| Features |
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| Applications | The Dicots SaCas9 Genome Editing Kit is applicable to modify genes in almost all kinds of dicots. |
| Resistance | Kanamycin |
| Selection Marker | Hygromycin B |
A: Hygromycin phosphotransferase (Hpt) is the most widely used selection marker which confers tolerance to the herbicide hygromycin because several crops have a natural tolerance to kanamycin.
A: The CRISPR/Cas systems are divided into two classes. The Class 1 systems have multiple Cas protein subunits, while the Class 2 systems utilize a single, multifunctional protein effector. Class 2 CRISPR systems are further divided into types II, V, and VI. In addition to the commonly used type II effector SpCas9, other orthologs with RNA-guided site-specific nuclease (SSN) activity have been engineered for use as tools in the genome editing of eukaryotic cells. These orthologs include proteins from Staphylococcus aureus (SaCas9), Francisella novicida (FnCas9), Neisseria meningitidis (NmCas9), Streptococcus thermophilus (St1Cas9), Brevibacillus laterosporus (BlCas9), and Campylobacter jejuni (CjCas9).
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SaCas9 is very suitable for soybean genome editing. We employed the Monocots SaCas9 Genome Editing Kit to successfully induce targeted mutations in five target sites of two soybean genes, GmFT2a and GmFT5a.
I recommend it. Dicots SaCas9 Genome Editing Kit has helped me to achieve site-specific knockout of target genes in hairy roots and regenerated plants of soybean to improve important agronomic characteristics.
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