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Seraseq® Trisomy 13 Female-Matched Reference Material

Seraseq® Trisomy 13 Female-Matched Reference Material

Seraseq® Trisomy 13 Female-Matched Reference Material

#0720-0780 Seraseq® Trisomy 13 Female - Matched Reference Material is intended for use in Whole Genome or Targeted Next Generation Sequencing (NGS) assays, dPCR, or microarray assays that screen for Trisomy 13 (Patau Syndrome) chromosomal abnormality in cell-free fetal DNA (cfDNA).
LGC SeraCare
€593.00 *

Prices plus VAT plus shipping costs

Delivery time 7 Workdays

Size: 1 x 1.0 ml (20 ng/ml)
  • Order number: 0720-0780
Description
Description
Seraseq® Trisomy 13 Female - Matched Reference Material is intended for use in Whole Genome or... more
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Seraseq® Trisomy 13 Female - Matched Reference Material is intended for use in Whole Genome or Targeted Next Generation Sequencing (NGS) assays, dPCR, or microarray assays that screen for Trisomy 13 (Patau Syndrome) chromosomal abnormality in cell-free fetal DNA (cfDNA). Seraseq® Trisomy 13 Female - Matched Reference Material is derived from DNA extracted from a pregnant patient source sample carrying a female fetus with confirmed Trisomy 13. This product is available in a simulated plasma format, enabelling the assessing the complete workflow from extraction through to analysis, similar to clinical samples. This reference material is intended for researchers and Non-Invasive Prenatal Testing (NIPT) labs to monitor library preparation, sequencing, and detection performance.

For additional information about the product, please visit the manufacturer's website.
DOWNLOADS 0720-0780IFU.pdf Seraseq® NIPT Reference Materials.pdf
PROPERTIES
storage temperature: 2-8°
shipping method: blue ice packs
regulatory status: RUO
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