Sequence Tagged Sites Technology Service

Sequence Tagged Sites Technology Service

With the continuous development of molecular biology, a new generation of molecular marker types have emerged, such as Sequence Tagged Site (STS), Sequence Charactered Amplified Region (SCAR), Candidate Gene (CG), etc. Sequence Tagged Site (STS), Sequence Charactered Amplified Region (SCAR), and Candidate Gene (CG) based on sequencing. The sequence tagged site (STS) is a short DNA sequence (200-500 bp) that occurs only once on a chromosome and whose position and base order are known. The greatest advantage of using STS is that it produces very reliable information.

Mapping of Sequence Tagged Sites.Figure 1. Mapping of Sequence Tagged Sites. (David PC, et al. 2013)

Unlike PCR with arbitrary primers, STS are primers that are based on some degree of sequence knowledge. These unique, sequence-specific primers detect variation in allelic, genomic DNA. STS have a particular advantage over RAPD in that they are codominant, that is, they can distinguish between homozygotes and heterozygotes. They also tend to be more reproducible, because they use longer primer sequences. However, they have the disadvantage of requiring some pre-existing knowledge of the DNA sequence of the region, even if only for a small amount.  The investment in effort and cost needed to develop the specific primer pairs for each locus is their primary drawback. As with RAPD, using PCR produces a quick generation of data and requires little DNA. All STS methods use the same basic protocols as RAPD (DNA extraction and PCR) and require the same equipment.

  • Most Common Sources
  • Any unique DNA sequence can be used as an STS. for a DNA sequence to be an STS, its sequence must be known so that the presence or absence of the STS in different DNA fragments can be detected by PCR. the STS must be uniquely localized on the chromosome to be studied or, when the DNA fragment population covers the entire genome, the STS must have a unique locus in the entire genome. If the STS sequence has multiple localization sites, the mapping data will be ambiguous. Therefore, it is necessary to ensure that the STS does not contain sequences of repetitive DNA.

  • What We Offer
  • Lifeasible has many years of experience in molecular markers, we provide STS technology solutions for global customers, we have a professional team to provide you with complete plant genomic DNA extraction and purification, STS-PCR primer design screening, sequence feature amplification region, and other project processes, with experienced experts to participate in the whole project, to supervise the project completion progress and quality, aiming to provide you with the best quality STS molecular marker services.

    • STS primer design and differential primer screening
    • STS-PCR amplification
    • STS marker polymorphism detection
    • STS marker validation
    • STS marker application development (genetic distance mapping, genetic diversity analysis, resistance gene screening analysis, etc.)
  • Service Flow
  • Service Flow

  • Applications
    • Genetic diversity analysis
    • Construction of genetic linkage maps
    • Localization of quantitative trait loci
    • Molecular marker-assisted breeding
    • Variety identification
  • Why Choose Lifeasible
    • We have extensive experience in STS marker development
    • Standardized processes to ensure accuracy of results
    • Data from all processes in the project are open to the client
    • Customized service system to meet all your needs
    • Best price/performance ratio
    • Optimized experimental process for fast results
  • How to Place an Order
  • How to Place an Order

    Lifeasible offers complete, professional STS technology service, as well as customized experimental protocols based on your project requirements and plant sample characteristics. For more information, please contact Lifeasible.

Reference:

  1. David PC, et al. (2013) Chapter 9 - Genomics & Systems Biology. Molecular Biology (Second Edition) 2013:248-272.
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