ehei (Thermo Fisher)
Structured Review
Ehei, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ehei/pm31529521-222-14-20
Average 90 stars, based on 1 article reviews
Images
Related Articles
Polymerase Chain Reaction:Article Title: Structural Basis for the Enzymatic Formation of the Key Strawberry Flavor Compound 4-Hydroxy-2,5-dimethyl-3(2H)-furanone Article Snippet: Cloning, Expression, and Purification of FaEO—FaEO was amplified via polymerase chain reaction (PCR) from pET29aFaQR (16) usingPfuDNApolymerase (Fermentas/ThermoScientific, St. Leon-Rot, Germany) and the phosphorothioate primers (18) 5 -GCC GCA GCT CCA AGT GAG TCC-3 und 5 -GTG GTG CCA TGG TTA GAT GGG ATA CAC AAC CAC C-3 , generating a 5 blunt end compatible with EheI and a 3 sticky end compatible with NcoI (both underlined). .. The PCR product was cut with NcoI (New England Biolabs, Ipswich, MA) and ligated with T4 DNA ligase (Fermentas/ Thermo Scientific) with the vector pASK-IBA5plus (IBA, Göttingen, Germany), which had been cut with Article Title: Structural Basis for the Enzymatic Formation of the Key Strawberry Flavor Compound 4-Hydroxy-2,5-dimethyl-3(2 H )-furanone Article Snippet: FaEO was amplified via polymerase chain reaction (PCR) from pET29a-FaQR ( 16 ) using Pfu DNA polymerase (Fermentas/Thermo Scientific, St. Leon-Rot, Germany) and the phosphorothioate primers ( 18 ) 5′- GCC GCA GCT CCA AGT GAG TCC-3′ und 5′-GTG GTG CCA TGG TTA GAT GGG ATA CAC AAC CAC C-3′, generating a 5′ blunt end compatible with EheI and a 3′ sticky end compatible with NcoI (both underlined). .. The PCR product was cut with NcoI (New England Biolabs, Ipswich, MA) and ligated with T4 DNA ligase (Fermentas/Thermo Scientific) with the vector pASK-IBA5plus (IBA, Göttingen, Germany), which had been cut with Purification:Article Title: Nucleic acid constructs for genome editing Article Snippet: .. DNA samples were analyzed for indel mutations using the restriction enzyme site loss method (Marton et al., 2010) Briefly, purified N. benthamiana DNA samples were first digested by |
