Sanger-EZ

Effortlessly unlock research success with Sanger-EZ, a convenient and reliable prepaid sequencing solution. Our kit of 96 pre-mixed barcoded tubes is designed to streamline research processes by eliminating the need for online ordering, enabling you to focus on the critical aspects of your research. With the introduction of our automated ordering system, Sanger-EZ offers the flexibility to submit all 96 samples at once or just one sample at a time. Simply order the kit directly from our online customer portal and submit samples in your nearest dropbox or via a local courier service.

Sanger-EZ Workflow

  • 1. Order Sanger-EZ Tubes

    Submit an order for the tubes on our online portal with your choice of delivery options

  • 2. Submit Pre-Mixed Samples

    Once received, fill tube(s) with template DNA + primer and submit sample(s) via your nearest dropbox or a courier service

  • 3. Sample Processing

    Our automated system creates the order online using the barcodes and our experts sequence your samples

  • 4. Data Delivery

    Results are shared via an email containing the link or can be accessed via our online portal

Features and Benefits

  • Convenience in Ordering – Sanger-EZ tubes eliminate the need for online orders
  • Industry-Leading TAT – Ph.D.-level project managers can deliver results within 24 hours after receiving your samples
  • High-Quality Data Delivery – Advanced automation technology ensures consistent delivery of the highest quality results while significantly reducing errors
  • Reliable Project Progress – With global production facilities and a local project manager, we offer a single-vendor solution to support your research

Technical Resources

  • Thumbnail for Sanger Sequencing Quick Tips guide

    Guide | Sanger Sequencing Quick Tips Guide

    Learn from the Sanger experts how you can get the most of your DNA Sequencing. Whether you’re troubleshooting a tough sequencing reaction, perfecting PCR visualization, or learning to clean up and refine your PCR products, these resources are designed to help you get the best results.

    • Volume 1: Producing Robust, Single-band PCR Product
    • Volume 2: PCR Clean-up of Single-band PCR
    • Volume 3: Salvaging Nonspecific PCR Products
    • Volume 4: PCR Visualization by Gel Electrophoresis
    • Volume 5: Troubleshooting a Bad Sequencing Reaction from a PCR Template
  • Thumbnail for blog post titled Troubleshooting DNA Templates with Sanger Sequencing

    Blog | Troubleshooting DNA Templates with Sanger Sequencing

    Sanger sequencing is highly effective for testing small targeted genomic regions and for validating results from NGS. However, as with all sequencing technologies, there are limitations and needs for troubleshooting. Read on to learn about the three basic troubleshooting steps we recommend to start with.

  • Thumbnail for webinar titled From Base Pairs to Breakthroughs: Understanding Sanger and Oxford Nanopore Sequencing

    Webinar | From Base Pairs to Breakthroughs: Understanding Sanger and Oxford Nanopore Sequencing

    While Sanger sequencing remains the gold standard for accurate DNA sequencing, advancements in sequencing technology, such as Oxford Nanopore Technology (ONT), have provided a cost-effective, long-read alternative for analysis. In this workshop, delve into the considerations of each technique and discover how to interpret their resulting sequencing data effectively so you can capture the benefits of both approaches for your specific needs.

  • Thumbnail for blog post titled Analyzing Sanger Sequencing Data

    Blog | Analyzing Sanger Sequencing Data

    The output for Sanger sequencing is typically a chromatogram, also known as a trace or ab1 file, and a text-based sequence file. Although the latter may seem to hold all the relevant information—after all, the point of sequencing is to get a sequence—the former can’t be ignored. Here, we provide a guide to understanding Sanger sequencing data.