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Ion Torrent™
Ion AmpliSeq™ Polyploidy Panel Kit with Ion GX5™ Chips (384 Samples)
The Genexus System-compatible Ion AmpliSeq Polyploidy Panel Kit empowers accurate quality controls in preimplantation genetic testing for aneuploidy (PGT-A) by了解更多信息
| 货号 | 数量 |
|---|---|
| GX55689 | 384 samples |
货号 GX55689
价格（CNY)
178,087.00
Each
数量:
384 samples
价格（CNY)
178,087.00
Each
The Genexus System-compatible Ion AmpliSeq Polyploidy Panel Kit empowers accurate quality controls in preimplantation genetic testing for aneuploidy (PGT-A) by leveraging SNP-based assessments.
Benefits of the Ion AmpliSeq Polyploidy Panel Kit include:
• Germline SNP detection from embryo biopsy samples—no parental DNA required, enabling the extraction of genetic insights directly from the sample
• Comprehensive genetic coverage—comprises 74 microhaplotype amplicons for human identification and 368 single SNP amplicons representing the population at large. With a total of 590 SNP sites covered, the panel unveils the unique genomic variations present in each sample, facilitating premium PGT-A analysis.
• Triploidy 69,XXX identification—through the utilization of tri-allelic microhaplotype sites and allele frequency distributions, samples with the potentially lethal triploidy 69,XXX can be confidently identified. This abnormality often appears similar to the normal 46,XX on conventional PGT-A plots, but the panel's advanced techniques help overcome this challenge.
• Mitigation of maternal contamination risk—reliable assessment of contamination from cumulus cell DNA made possible by tri-allelic microhaplotype sites. This assessment assists in prioritizing low-risk samples with minimized maternal contamination concerns.
• Sibling embryo tracking—SNP clustering allows for the identification of genetically related embryos, helping prevent sample mix-ups. This functionality ensures that the most suitable embryos progress accordingly in the reproductive journey, optimizing the selection process.
Enhance sample prioritization in PGT-A through the implementation of SNP-based quality controls
Single nucleotide polymorphisms (SNPs) are unique genetic variations that can be inherited and directly associated with parental DNA. By leveraging SNPs, PGT-A analysis gains valuable insights into triploidy 69,XXX, maternal contamination, helping ease the selection of embryos for IVF reseach.
Notes
• This kit is compatible with the Genexus System.
仅供研究使用。
规格
数量384 samples
产品规格试剂盒
测序类型新一代测序
Unit SizeEach
内容与储存
• Ion AmpliSeq Polyploidy Panel, –10 to –30°C
• Ion AmpliSeq Lib Kit Plus, –10 to –30°C
• Genexus Cartridge, –10 to –30°C
• Genexus Bottle 2, 15–30°C
• Genexus Bottle 1 and 3, 15–30°C
• Genexus Strip 3-GX5, 2–8°C
• Genexus Strip 4, –10 to –30°C
• Genexus Coupler and GX5 Chip, 15–30°C
• Ion AmpliSeq Lib Kit Plus, –10 to –30°C
• Genexus Cartridge, –10 to –30°C
• Genexus Bottle 2, 15–30°C
• Genexus Bottle 1 and 3, 15–30°C
• Genexus Strip 3-GX5, 2–8°C
• Genexus Strip 4, –10 to –30°C
• Genexus Coupler and GX5 Chip, 15–30°C