PEA CRISPR Plasmide
Santa Cruz Biotechnology, Inc. bietet eine Vielzahl von Produkten zur Editierung von Genen an einschließlich CRISPR/Cas9 Knockout und CRISPR Double Nickase Plasmide für das Gen Silencing. PEA Gen Silencer sind erhältlich als PEA CRISPR/Cas9 Knockout Plasmide und PEA Double Nickase Plasmide. PEA CRISPR/dCas9 Aktivierungsplasmide und CRISPR Lenti Aktivierungssysteme für die Aktivierung von Genen sind ebenfalls erhältlich. Gen Silencer und Aktivatoren sind äußerst hilfreich bei der Untersuchung von Genen in Kombination mit den Antikörpern zur Detektion entsprechender Proteine.
PEA CRISPR Knockout, HDR and Double Nickase Plasmids
| Empty Table Header | Produkt | Katnr. | Species | Anwendungen | MARKER | Referenzen | Bewertung |
|---|---|---|---|---|---|---|---|
PEA3 CRISPR/Cas9 KO Plasmid (h2) | sc-401704-KO-2 | h | Gene Knockout | GFP | 0 | ||
PEA3 HDR Plasmid (h2) | sc-401704-HDR-2 | h | Homology Directed Repair | Puromycin | 0 | ||
PEA3 Double Nickase Plasmid (h) | sc-401704-NIC | h | Gene Knockout | Puromycin | 0 | ||
PEA3 Double Nickase Plasmid (h2) | sc-401704-NIC-2 | h | Gene Knockout | Puromycin | 0 | ||
PEA3 CRISPR/Cas9 KO Plasmid (m) | sc-422185 | m | Gene Knockout | GFP | 1 | ||
PEA3 HDR Plasmid (m) | sc-422185-HDR | m | Homology Directed Repair | Puromycin | 1 | ||
PEA3 Double Nickase Plasmid (m) | sc-422185-NIC | m | Gene Knockout | Puromycin | 1 | ||
PEA3 Double Nickase Plasmid (m2) | sc-422185-NIC-2 | m | Gene Knockout | Puromycin | 1 | ||
PEA-15 CRISPR/Cas9 KO Plasmid (h) | sc-416336 | h | Gene Knockout | GFP | 0 | ||
PEA-15 HDR Plasmid (h) | sc-416336-HDR | h | Homology Directed Repair | Puromycin | 0 | ||
PEA-15 Double Nickase Plasmid (h) | sc-416336-NIC | h | Gene Knockout | Puromycin | 0 | ||
PEA-15 Double Nickase Plasmid (h2) | sc-416336-NIC-2 | h | Gene Knockout | Puromycin | 0 | ||
PEA-15 CRISPR/Cas9 KO Plasmid (m) | sc-422184 | m | Gene Knockout | GFP | 0 | ||
PEA-15 HDR Plasmid (m) | sc-422184-HDR | m | Homology Directed Repair | Puromycin | 0 | ||
PEA-15 Double Nickase Plasmid (m) | sc-422184-NIC | m | Gene Knockout | Puromycin | 0 | ||
PEA-15 Double Nickase Plasmid (m2) | sc-422184-NIC-2 | m | Gene Knockout | Puromycin | 0 |
PEA CRISPR Activation Products
| Empty Table Header | Produkt | Katnr. | Species | Anwendungen | MARKER | Referenzen | Bewertung |
|---|---|---|---|---|---|---|---|
PEA3 CRISPR Activation Plasmid (h) | sc-401704-ACT | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA3 CRISPR Activation Plasmid (h2) | sc-401704-ACT-2 | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA3 Lentiviral Activation Particles (h) | sc-401704-LAC | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA3 Lentiviral Activation Particles (h2) | sc-401704-LAC-2 | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA3 CRISPR Activation Plasmid (m) | sc-422185-ACT | m | Gene Activation | Puro, Blast, Hygro | 1 | ||
PEA3 CRISPR Activation Plasmid (m2) | sc-422185-ACT-2 | m | Gene Activation | Puro, Blast, Hygro | 1 | ||
PEA3 Lentiviral Activation Particles (m) | sc-422185-LAC | m | Gene Activation | Puro, Blast, Hygro | 1 | ||
PEA3 Lentiviral Activation Particles (m2) | sc-422185-LAC-2 | m | Gene Activation | Puro, Blast, Hygro | 1 | ||
PEA-15 CRISPR Activation Plasmid (h) | sc-416336-ACT | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 CRISPR Activation Plasmid (h2) | sc-416336-ACT-2 | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 Lentiviral Activation Particles (h) | sc-416336-LAC | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 Lentiviral Activation Particles (h2) | sc-416336-LAC-2 | h | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 CRISPR Activation Plasmid (m) | sc-422184-ACT | m | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 CRISPR Activation Plasmid (m2) | sc-422184-ACT-2 | m | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 Lentiviral Activation Particles (m) | sc-422184-LAC | m | Gene Activation | Puro, Blast, Hygro | 0 | ||
PEA-15 Lentiviral Activation Particles (m2) | sc-422184-LAC-2 | m | Gene Activation | Puro, Blast, Hygro | 0 |