Sanger Premix Sequencing

4,40336,00

Select the number of each type of sample you want to sequence.

IMPORTANT : To sequence and analyse your samples, our laboratory needs all the details asked in the Sample Sheet.

1. Download and fill in the SampleSheet.

2. Drag & drop  SampleSheet + Reference below in case you have a Reference in fasta format (.fasta or .fa) available.

Providing us with a Reference improves the quality of the Bioinformatic analysis.

3. Place your order.

4,40
336,00

Upload your files below

Sample Sheet *


Fasta Files


Description

Our Sanger Sequencing service offers a streamlined and precise solution for sequencing your DNA samples, utilizing primers provided directly by you in the same tube. This service is perfect for researchers who already have custom primers or specific sequences in mind for their project. By submitting both the DNA sample and primers together, we ensure a seamless process with optimal results.

Key Features:

  • High-Quality Sequencing: Our Sanger sequencing platform provides reliable, high-accuracy results with long read lengths, making it ideal for small to medium-sized DNA sequences.
  • Customer-Supplied Primers: You provide the primers, and we handle the rest. Simply submit your DNA and primers together in the same tube, and we will ensure they are used effectively in the sequencing process.
  • Flexible Application: This service is suitable for a wide range of applications, including sequencing plasmids, PCR products, gene fragments, and other targeted DNA regions where custom primers are required.
  • Accurate Detection of Variants: Sanger sequencing is well-suited for detecting small genetic changes such as point mutations, SNPs, and indels with high precision.
  • Fast and Efficient: We offer a fast turnaround time, ensuring you get your sequencing results quickly to keep your research moving forward.

 

With our PREMIX Sanger Sequencing service, you’ll receive accurate, reliable results quickly, with a simple and efficient process. If you have custom primers and a specific sequencing request, this service provides the flexibility and precision you need for your research.