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Image Search Results
a " width="100%" height="100%">
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Complete List of Golden Gate Toolkits Following the Common Syntax
Article Snippet:
Techniques: Marker, Transformation Assay, Expressing, Ubiquitin Proteomics, Selection, Plasmid Preparation, Infection, Cloning, CRISPR, Bacteria
a " width="100%" height="100%">
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Alternative Golden Gate Methods That Do Not Follow the Common Syntax
Article Snippet:
Techniques: Selection, Expressing, Marker
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Proper design of restriction sites. For Golden Gate assembly to be successful, all part vectors must have inward-facing Type IIS sites, so that the enzyme recognition sequence is in the backbone (not the part); at the same time, destination vectors must have outward-facing sites, with the recognition sequence in the part (not the backbone). Also, the sequence of the fusion sites must be chosen so that parts that will be adjacent in the final assembly have complementary fusion sites. Clearly, the destination vector must have sites complementary to the first and the last fusion sites in the assembly, so that the entire construct will ligate into the destination vector.
Article Snippet: MoChlo: Modular Cloning Chloroplast Toolbox ,
Techniques: Sequencing, Plasmid Preparation, Construct
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Destination vectors as acceptor backbones. The destination vector of a Golden Gate assembly provides the origin or replication and selection marker of the final construct (dashed box). Note that the fusion sites of the destination vector (<>) appear in the opposite orientation compared to those of the part vectors (><). The cargo of the destination vector (gray CDS) is a dropout marker, which is lost during the assembly. Therefore, the final construct can be isolated by combining positive selection for the backbone marker (typically antibiotic resistance), and negative screening against the dropout marker (usually a visual marker such as lacZα ).
Article Snippet: MoChlo: Modular Cloning Chloroplast Toolbox ,
Techniques: Plasmid Preparation, Selection, Marker, Construct, Isolation
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Multilevel hierarchical assembly. If a destination vector contains inward sites in addition to outward sites, the inward sites will be retained in the final assembly and can then be used to excise the product as if it was a part. In this example, both destination vectors have the same outward-facing sites (blue<>yellow), but different inward-facing sites (respectively blue> Article Snippet: MoChlo: Modular Cloning Chloroplast Toolbox , Techniques: Plasmid Preparation, Marker
a " width="100%" height="100%">
Journal: ACS Synthetic Biology
Article Title: A User’s Guide to Golden Gate Cloning Methods and Standards
doi: 10.1021/acssynbio.2c00355
Figure Lengend Snippet: Complete List of Golden Gate Toolkits Following the Common Syntax
Article Snippet: MoChlo: Modular Cloning Chloroplast Toolbox ,
Techniques: Marker, Transformation Assay, Expressing, Ubiquitin Proteomics, Selection, Plasmid Preparation, Infection, Cloning, CRISPR, Bacteria