Part:BBa_K3841023
pGGAselect Destination Plasmid
pGGAselect destination plasmid is a 2,220 bp cloning vector useful for Golden Gate Assembly desgined by New England Biolabs (NEB) [1]. The plasmid contains two BsaI, BsmBI and BbsI restriction sites; digestion with BsmBI releases an 87 bp fragment and a 2,133 bp vector backbone fragment to receive your insert or assembly. Below is the pGGAselect plasmid map from NEB Golden Gate Assembly Kit (BsaI-H®v2) protocol.
Usage
pGGAselect is suitable for Golden Gate Assembly. Either digest the backbone with BsaI or BsmBI for prepare it for insert or assembly.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 296
Illegal EcoRI site found at 434
Illegal PstI site found at 234 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 296
Illegal EcoRI site found at 434
Illegal PstI site found at 234
Illegal NotI site found at 445 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 296
Illegal EcoRI site found at 434
Illegal BglII site found at 356
Illegal BamHI site found at 290
Illegal XhoI site found at 284
Illegal XhoI site found at 439 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 296
Illegal EcoRI site found at 434
Illegal PstI site found at 234 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 296
Illegal EcoRI site found at 434
Illegal PstI site found at 234 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 395
Illegal BsaI.rc site found at 320
References
[1] New England Biolabs, url: https://international.neb.com/-/media/nebus/page-images/tools-and-resources/interactive-tools/dna-sequences-and-maps/text-documents/pggaselectfsa.txt?rev=87941bf93a1d49f28c69930c8289e15f&hash=4A71E1E81374F863510F52544BA65704
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