The restriction enzymes Xho I and Xba I were used to digest a linear fragment of DNA at specific sequences such as that shown for EcoRI (figure above).Use the information gained from
Anne's paper on Easy Expression and Purification of Fluorescent N-Terminal BCL11B CCHC Zinc Finger Domain is published - Fakultät - Universität Greifswald
Oligonucleotide primers to introduce XhoI and ApaI restriction sites... | Download Table
XhoI | NEB
Sequences of oligonucleotide primers Restriction enzyme sites... | Download Table
SciELO - Brasil - In-Situ Gel-Free Plasmid Reassembling for Rapid Gene Subcloning and Truncation In-Situ Gel-Free Plasmid Reassembling for Rapid Gene Subcloning and Truncation
XhoI Restriction Enzyme - Laboratory Notes
SciELO - Brasil - In-Situ Gel-Free Plasmid Reassembling for Rapid Gene Subcloning and Truncation In-Situ Gel-Free Plasmid Reassembling for Rapid Gene Subcloning and Truncation
Protocol for preparing NdeI and XhoI Double Digest Reactions – BBS OER Lab Manual
20.109(F16):Complete in silico cloning (Day1) - Course Wiki
XhoI | NEB
SOLVED: #16) The restriction enzymes Xhol and SalI cut their specific sequences as shown below: XhoI 5' C | TCGAG 3' SalI | 5' GTCGAC 3' 3' GAGC | TC 5' 3'