维百奥(北京)生物科技有限公司

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产品名称 Seraseq® 22q11 Female-Matched Reference Material (SeraCare)
目录号 0720-0174
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品名:Seraseq® 22q11 Female-Matched Reference Material

货号:0720-0174 

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 22q11 Female Matched 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 22q11 (or DiGeorge Syndrome) female 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 strick quality checks

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

buffer format) available on request/li> 


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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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