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Frequently Asked Questions - Sanger Sequencing
Product & Services
The Barcode Economy Run is Microsynth Seqlab‘s most demanded standard sequencing service for plasmids and PCR products in 1.5 ml tubes. It offers the best price-performance ratio due to its prepayment structure (minimally 50 barcode labels corresponding to 50 sequencing reactions have to be purchased in advance).
Microsynth Seqlab’s Economy Run corresponds to the Barcode Economy Run, with the exception that customers will be invoiced after using the service and they are not bound to batches of 50 barcodes.
The Premium Run is Microsynth Seqlab‘s superior sequencing service in 1.5 ml tubes offering a broad spectrum of additional services (e.g. Reaction conditions are optimized specifically for your sample and special treatment protocols for difficult sequences) and troubleshooting protocols (e.g. alternative design of sequencing primers, one-drop sequencing in case of low DNA amounts).
Generally speaking, the Premium Run is designed for customers requiring the best possible outcome along with superior service.
Please login to our webshop to find a sample drop box in your vicinity.
- Barcode Economy Run or Economy Run Service samples: 4 working days
- Premium Run Samples: 3 months
- High-Throughput sample plates: 1 month
- Your specific sequencing primers will be kept at our sequencing lab for at least 6 months (or for 12 months in case you have added them to your “Custom Primer List”).
On request, Microsynth Seqlab will ship your specific sequencing primer(s) back to your or any other desired address.
Click here to open our standard primer list with all the primers you can select from.
Please note: Microsynth’s webshop allows you to maintain a customized primer list. In case you frequently use more specific sequencing primers, just send them to Microsynth and update your customized primer list. Since Microsynth operates a well-recognized oligo production facility, you can also outsource design and/or synthesis of your sequencing primers.
Yes, it is possible to send samples in one 96-well plate and request multiple reactions (with two or more primers) for each sample.
First option: identical sample from same well position with more than one primer. You send 12 ul of the sample for the first reaction plus 3 ul of the sample for each additional reaction.
You specify the sequencing reactions of the plate you're going to send physically (= master plate) indicating the first primer(s). Under "Review order" you can copy the sample pattern of the master plate (use the button "copy"). Just be aware that for our Barcode High-Throughput Run you need another prepaid barcode label. Whereas the label number is entered into the system, the label should be attached to the master plate. Theoretically, it is possible to repeat this step several times (for further primers).
If the master plate is not entirely filled, we recommend switching to our non-prepaid High-Throughput Run and following the same ordering scheme (exception: use the same plate name).
Second option: identical sample from different well positions with more than one primer
If you're using the Barcode High-Throughput Run and you want us to sequence half of the samples with the forward primer and the other half of the samples with the reverse primer you should provide the samples in two separate wells e.g. A01-H06 with forward primer and A06- H12 with reverse primer.
Order Related Questions
Dependent on the selected service type, your samples have to fulfill different requirements. For following services, Microsynth Seqlab provides user guides containing a lot of helpful information:
Please click on the name of the service above to open the relevant user guide; or go to the “Sample Requirements” area where you will also find useful information about sample requirements etc.
- Enter our webshop
- Click on Option&Preferences in the DNA Sequencing area
- Click on Order History - Review/Delete Previous Orders
In general, failed sequencing reactions will be automatically repeated in the following mode: in a first attempt one sample will be repeated in order to evaluate the potential for further improvement by modifying the chemistry of the sequencing reaction. If the repetition yields in a better sequencing result, other samples of your order will be resequenced, too. In addition, it is always possible to ask for specific repetitions of failed reactions (best done by phone or email). Be aware, that we keep Economy and Barcode Economy Run samples only for 4 working days.
Genetically modified microorganisms (GMOs) that do not meet the definition of toxic or infectious substances, but are able to modify animals, plants or microbial substances in a way that does not normally result from natural reproduction, do belong to Class 9 and shall be assigned to UN3245 and shipped in accordance with Packing Instruction P904.
In short, this means the samples must be packed in an inner, a secondary and an outer packaging. The inner packaging comprises of a leakproof primary receptacle and an absorbent material placed between the primary receptacle and the secondary packaging (e.g. plastic bag). The outer packaging shall be strong enough for its capacity, mass and intended use and shall have a minimum outer dimension of at least 100 mm.
Further information can be found at https://adrbook.com/en/2017/Sutun/8/P904.
If GMOs cannot be assigned to UN3245/class 9 (which is true for most E. coli laboratory strains and vectors), they are not subject to dangerous goods regulations.
GMOs are not subject to the dangerous goods regulations if they are approved for use by the competent authorities of the countries of origin, transit and destination.
Go to the “Sequencing Primers” area where you will find a lot of useful information about sequencing primers.
Microsynth provides the sequencing results in text format (FASTA files) and in chromatogram format (ab1 files). In order to open the ab1 files you need to download one of the software tools which are provided in the Software and Links area.
Direct sequencing via the Sanger approach is possible for genomes < 1Mb. However, whenever feasible, we recommend you to amplify the region of interest by PCR and to send us the PCR product(s) for sequencing.
In order to obtain reliable sequencing results, impurities such as dNTPs, PCR primers etc. must be eliminated. Furthermore, it is important to quantify the purified PCR product. This is easily accomplished by performing agarose gel electrophoresis of your PCR product and comparing the band for your PCR product with standard bands of defined concentrations. We do not recommend quantification approaches based on UV spectrophotometric analysis techniques. For successful sequencing, PCR products must be single-banded on the agarose gel. If this is not the case, you should recover the correct band by gel extraction. Using the Premium Run we can do this for you.
The results of the Sanger sequencing are kept for at least 3 months on the webshop.