维百奥(北京)生物科技有限公司

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产品名称 Seraseq® Triple X Syndrome (XXX) Reference Material (SeraCare)
目录号 0720-1069
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品名:Seraseq® Triple X Syndrome (XXX) Reference Material

货号:0720-1069

品牌:SeraCare 


Details

Given the clinical implications, it is extremely critical that NIPT assays report back presence or absence of aneuploidies 

in an accurate and consistent manner. Matched maternal-fetal reference materials derived from pregnant maternal 

plasma enable accurate assessment of a broad range of NIPT assays, including those based on counting methods, 

SNPs, as well as differences in the length of maternal and fetal cfDNA. 

The Seraseq Triple X SYndrome (XXX) Reference Material can be used to develop a new test, validate an assay, monitor 

routine performance, troubleshoot problems across the entire workflow, and ensure overall proficiency with the same 

sustainable product. 

Matched (or related) maternal-fetal Triple X Syndrome (or Trisomy XXX) sample compatible with a broad range of 

NIPT assay methods 

Proprietary method maintains native cfDNA characteristics such as size profile of ~170 bp, size distribution, SNP 

content, and natural maternal-fetal size difference.

Offered in a plasma format capable of assessing the entire workflow from extraction through analysis (identical to 

clinical samples) Long shelf-life and lot-to-lot consistency with high-quality materials manufactured in 

GMP-compliant and ISO 13485-certified facilities under strict quality checks.

Customization of fetal fraction, concentration, and material formulation (either in plasma or fragmented DNA in 

buffer format) available on request.


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维百奥生物代理SeraCare对照及参比物质。


维百奥(北京)生物科技有限公司,自2018年与SeraCare(现隶属于LGC Clinical Diagnostics)合作以来,长期为中国客户

提供包括SeraSeq系列参比物质,领域包括肿瘤、生殖健康遗传病。SeraCare研发和生产一系列临床参比物质,可以用于任何

研发阶段,以确保临床基因组学检测结果的准确性。

 

SeraCare参比物质涵盖的范围:

1)Next Generation Sequencing

2)Sanger Sequencing

3)Real-time PCR and digital PCR (dPCR)

4)Microarray

 

主要特点

1)Ready-to-use reference materials covering clinically-relevant variants and all variant types - SNVs, INDELS, CNVs, 

and RNA fusions

2)Highly multiplexed - provide significantly more data per NGS run, saving sequencing costs

3)Available in multiple formats to suite different workflow needs - purified DNA & RNA, ctDNA, encapsulated ctDNA 

in plasma, and FFPE

4)Manufactured in cGMP-compliant, ISO 13485-certified facilities

5)Stringent product release testing - all variants qualified by dPCR for allele frequencies or copy numbers

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