![]() ![]() This button will be disabled if the program detects an internal site in your insert sequence. As you can see, the graphic now shows both the pGGAselect vector backbone and the first insert. For our demonstration, however, we will use the entire sample insert sequences in the appropriate orientation as shown. If your insert sequence is part of an uploaded plasmid construct, it is important to identify the uploaded sequence as being circular in case your insert spans the beginning of the presumed linear sequence file. You can also generate the reverse complement if this is required for the correct orientation of your building assembly. If loading your own insert sequence, you have the option of designating the beginning and end of the desired insert sequence by entering the “Start” and “End base” numbers from your uploaded sequence. Next, select “PCR-generated BsmBI-v2 sites” to automatically build flanking BsmBI sites in the primer designed for your insert PCR. Notice the vector and circular identifiers have not been checked as the entire sequence in the sequence window should be the desired insert. The sequence will now appear in the parsed sequence window and the insert name will be shown. Select “Insert 1” from the sample inserts dropdown menu. The graphic should now show the pGGAselect vector backbone. For other proposed destination plasmids, the tool will warn you if sites are not present or if they are improperly oriented. Since pGGAselect already has designed flanking BsaI, BsmBI, and BbsI sites at the assembly site of the plasmid. Next, select “Existing BsmBI-v2 cut sites”. Note the destination vector has been identified as your vector and as circular. You will also have the option of using the sequence or converting it to its reverse complement to fit in the correct orientation in your desired final assembly. If you are loading your own destination vector sequence, you can paste it in manually or load your GenBank, FASTA, or raw sequence file. The sequence will appear in the parsed sequence window and the vector name will be shown. Then select “pGGAselect” from the destination vector's dropdown menu. ![]() Add the destination vector by clicking on “Add Sequence”. In our example, we will select “BsmBI-v2” and use sequences that have no internal sites.Īdd the destination vector. If this is not possible, view our video on Golden Gate Domestication for strategies dealing with internal sites. Choose the restriction enzyme that has no internal sites in the DNA sequences to be used in the assembly. Enzymes available from NEB are shown in red. The tool will help design PCR primers to make amplicon inserts, check sequences for internal Type IIS restriction enzyme cut sites, and generate a report that shows the assembly graphically, and includes a full construct sequence file.īegin by selecting the Type IIS restriction enzyme you have chosen for your assembly design from the dropdown menu. As an example, we will build an assembly from five sample inserts or modules using the pGGAselect destination plasmid supplied with our Golden Gate Assembly Kits. In this video, we will demonstrate how to use the NEB Golden Gate Assembly Tool. ![]() ![]() This MCU can run at max 32Mhz instead of max 16Mhz.Tutorial for NEB Golden Gate Assembly Tool. The board I have has a WAVGAT AVGA328P MCU, which is actually a Light Green LGT8F328P MCU instead of a the original Atmel/Microchip ATMEGA328P. put your main code here, to run repeatedly: put your setup code here, to run once: After uploading the same code, the clockspeed looks okay however no serial output at all (tried every baud speed available at the serial monitor). Then I download the board definitions for the WAVGAT clones and select "WAVGAT Pro Mini". Serial however works in this situation but at 2400 baud instead of 9600 baud (Serial was initialized with 9600 baud). The first problem was it is running too slow (4x slower) when compiling with default "Pro or Pro Mini" board profile. I ordered some Pro Minis however get some WAVGAT clone thingies. ![]()
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