![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 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](https://minio.scielo.br/documentstore/1678-4324/TLWwbvLPXTpR3FPZJd8Ldws/5d5628564867190f1660b052e983f57cf481a7e8.png)
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
![Useful tool to generate unidirectional deletion vectors by utilizing the star activity of BamHI in an NcoI-BamHI-XhoI cassette | BioTechniques Useful tool to generate unidirectional deletion vectors by utilizing the star activity of BamHI in an NcoI-BamHI-XhoI cassette | BioTechniques](https://www.future-science.com/cms/10.2144/05382BM05/asset/images/medium/figure1.gif)
Useful tool to generate unidirectional deletion vectors by utilizing the star activity of BamHI in an NcoI-BamHI-XhoI cassette | BioTechniques
![Anne's paper on Easy Expression and Purification of Fluorescent N-Terminal BCL11B CCHC Zinc Finger Domain is published - Fakultät - Universität Greifswald Anne's paper on Easy Expression and Purification of Fluorescent N-Terminal BCL11B CCHC Zinc Finger Domain is published - Fakultät - Universität Greifswald](https://biochemie.uni-greifswald.de/storages/uni-greifswald/fakultaet/mnf/biochemie/delcea/Research/anne_bcl11b_molecules1.png)
Anne's paper on Easy Expression and Purification of Fluorescent N-Terminal BCL11B CCHC Zinc Finger Domain is published - Fakultät - Universität Greifswald
![XhoI Restriction Enzyme Antisense RNA Restriction Site Nucleic Acid, PNG, 1972x677px, Restriction Enzyme, Antisense Rna, Area, XhoI Restriction Enzyme Antisense RNA Restriction Site Nucleic Acid, PNG, 1972x677px, Restriction Enzyme, Antisense Rna, Area,](https://img.favpng.com/5/3/14/xhoi-restriction-enzyme-antisense-rna-restriction-site-nucleic-acid-png-favpng-YRJ5wV7HGALxrkZfLSPaRCMYc.jpg)
XhoI Restriction Enzyme Antisense RNA Restriction Site Nucleic Acid, PNG, 1972x677px, Restriction Enzyme, Antisense Rna, Area,
![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 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](https://haygot.s3.amazonaws.com/questions/529874_1b792d0ddcb047e78048832bb5296b8a.png)
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
![A) Restriction enzyme digestion with Xho I and Nco I of the constructs... | Download Scientific Diagram A) Restriction enzyme digestion with Xho I and Nco I of the constructs... | Download Scientific Diagram](https://www.researchgate.net/publication/13373235/figure/fig1/AS:281653143457793@1444162750028/A-Restriction-enzyme-digestion-with-Xho-I-and-Nco-I-of-the-constructs-pET20b-CAT.png)
A) Restriction enzyme digestion with Xho I and Nco I of the constructs... | Download Scientific Diagram
![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 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](https://minio.scielo.br/documentstore/1678-4324/TLWwbvLPXTpR3FPZJd8Ldws/c278804ee2c336f7b0b19763afdc5ec5bd959d67.png)
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
![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' 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'](https://cdn.numerade.com/ask_previews/21874a29-d8b1-4bc7-8a95-3be31c0a8eb4_large.jpg)
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'
![SOLVED: 1. Thee restriction enzyme Sal I cuts the sequence GTCGAC to leave a four base, 5' overhangg. The restriction enzyme XhoI cuts the sequence CTCGAG to leave a four base, 5' SOLVED: 1. Thee restriction enzyme Sal I cuts the sequence GTCGAC to leave a four base, 5' overhangg. The restriction enzyme XhoI cuts the sequence CTCGAG to leave a four base, 5'](https://cdn.numerade.com/ask_previews/314f1313-7c1f-4b5b-8cf3-51ef84278a47_large.jpg)
SOLVED: 1. Thee restriction enzyme Sal I cuts the sequence GTCGAC to leave a four base, 5' overhangg. The restriction enzyme XhoI cuts the sequence CTCGAG to leave a four base, 5'
![Primer sequences. Cleavage sites for the restriction enzymes NheI and... | Download Scientific Diagram Primer sequences. Cleavage sites for the restriction enzymes NheI and... | Download Scientific Diagram](https://www.researchgate.net/publication/332468634/figure/tbl2/AS:756641469317122@1557408792850/Primer-sequences-Cleavage-sites-for-the-restriction-enzymes-NheI-and-XhoI-appears.png)