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Genetic Analysis: Cell Line Authentication (STR Analysis) Contract Analysis Service

For the identification and authentication of human cell lines and the detection of cross-contamination within the same cell line!

Our company offers a cell line authentication (STR analysis) contract analysis service. We determine the STR (short tandem repeat) genotype from samples derived from human cultured cells. We use the GenePrint® System (10 loci) or the PowerPlex® 16 System (16 loci). Please use this service for the identification and authentication of human cell lines, as well as for detecting cross-contamination within the same type of cell lines. 【Features】 - Determine STR genotype from samples derived from human cultured cells. - Use the GenePrint® System, which is suitable for the identification and authentication of human cell lines and for detecting cross-contamination within the same type of cell lines. - Use the PowerPlex® 16 System, which is suitable for confirming the genotype of iPS/ES cells. - We can provide a free English report for customers who wish to submit it for publication. *For more details, please refer to the PDF materials or feel free to contact us.

  • Contract Analysis

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miRNA contract analysis service "PanoramiR"

Utilizing patented technology, miRNA measurement with excellent "specificity," "detection sensitivity," and "reproducibility." An optimal service for biomarker discovery and disease mechanism analysis.

HMT has partnered with MiRXES, a company based in Singapore, to provide miRNA (microRNA) analysis services. The ID3EAL technology, which utilizes MiRXES's patented technology, offers an excellent method for miRNA measurement with high specificity, detection sensitivity, and reproducibility, supporting your research and development. One of our contract analysis services, the 'PanoramiR miRNA KNOWLEDGE PANEL,' is a contract analysis service that uses a profiling panel of 376 carefully selected miRNAs related to various diseases. The target miRNAs are selected based on databases such as miRbase 22, HMDD v3.2, The Cancer Genome Atlas, as well as our own research and influential academic papers. This service is recommended for basic research in biomarker discovery and disease mechanism analysis. *For more details, please refer to the link below or feel free to contact us.*

  • Public Testing/Laboratory

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