CRISPR/Cas9
CRISPR stands for "Clustered regularly interspaced short palindromic repeats". They were discovered in prokaryotic DNA first in 1987 and contain short repetitions of base sequences. In the course of better sequencing techniques in the early 2000s similar sequences were found in other bacteria as well. Further research revealed that the sequences of repeats in Bacteria chromosomes is interspaced with sequences derived from viruses. So called Cas proteins (CRISPR-associated genes) encodes putative nuclease or helicase proteins. Today we know that the CRISPR-System helps bacteria to acquire a type of immune system. For a short introduction to CRISPR please visit our CRISPR resource page here.
genomics-online offers you currently more than 300,000 Cas9 enzyme products and ready-to-use plasmids for CRISPR/Cas9. Your advantages: Lower price than customized and faster results. Below you will find all of our CRISPR/Cas9 products.
Click here to visit our CRISPR-plasmid category, or here to see all of our Cas9 enzyme products. If you need help with finding the right product for your needs, our customer support will gladly help you via phone, live chat or email.
Recommended next Filters:
269,459 results :
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 1000 nM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Concentration:
- 10 μM
- Application:
- Genome Editing with Engineered Nucleases
- Type:
- gRNA + Cas9
- Application:
- Protein Expression, Genome Editing with Engineered Nucleases
- Gene:
- phosphoserine Aminotransferase 1 (PSAT1)
- NCBI Accession:
- NM_177420
- Species:
- Mouse
- Vector type:
- Lentiviral Vector
- Vector backbone:
- pLenti-U6-sgRNA-SFFV-Cas9-2A-Puro
- Resistance Gene:
- Ampicillin
- Selection Marker:
- Puromycin
- Promoter:
- U6 Promoter, SFFV Promoter
- Expression:
- Stable, Transient
- Type:
- gRNA + Cas9
- Application:
- Protein Expression, Genome Editing with Engineered Nucleases
- Gene:
- phosphoserine Aminotransferase 1 (PSAT1)
- NCBI Accession:
- NM_021154
- Species:
- Human
- Vector type:
- Lentiviral Vector
- Vector backbone:
- pLenti-U6-sgRNA-SFFV-Cas9-2A-Puro
- Resistance Gene:
- Ampicillin
- Selection Marker:
- Puromycin
- Promoter:
- U6 Promoter, SFFV Promoter
- Expression:
- Stable, Transient
- Type:
- gRNA + Cas9
- Application:
- Protein Expression, Genome Editing with Engineered Nucleases
- Gene:
- Prune Homolog (Drosophila) (PRUNE)
- NCBI Accession:
- NM_001007697
- Species:
- Rat
- Vector type:
- Lentiviral Vector
- Vector backbone:
- pLenti-U6-sgRNA-SFFV-Cas9-2A-Puro
- Resistance Gene:
- Ampicillin
- Selection Marker:
- Puromycin
- Promoter:
- U6 Promoter, SFFV Promoter
- Expression:
- Stable, Transient
