产品名称 | Seraseq® Unmethylated ctDNA Mutation Mix (SeraCare) |
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目录号 | 0710-3088 |
别名 | N/A |
外观 | N/A |
分子量 | N/A |
CAS | N/A |
溶解度 | N/A |
存储条件 | N/A |
保存时间 | N/A |
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目录号 | 规格 | 价格 | 库存状态 | |
0710-3088 | 1 x 25 µl | 咨询客服 | 咨询客服 |
品名:Seraseq® Unmethylated ctDNA Mutation Mix
货号:0710-3088
品牌:SeraCare
Product Specifications
% Methylation:<2%
Fragment Size Peak:155-220
Concentration:10ng/pL
Fill Size:25 L
Total DNA:250 ng
Buffer:0.1x TE
Details
The use of ctDNA in the study and treatment of cancer continues to expand. Recent advances have highlighted
CpG methylation of ctDNA a biomarker with multiple utilities. Methylation status gives insight to tumor
recurrence, epigenetic regulation of gene expression and may also indicate tissue of origin of ctDNA.
Despite the impactful layer of information methylation status adds to base-pair level sequencing data and the
proliferation of assays to incorporate methylation data, reference materials have been limited compared to
other areas of oncology. Seraseq Unmethylated ctDNA Mutation Mix is a low background ctDNA reference
material comprised of ctDNA that is unmethylated (<2% detectably methylation) at all cpg sites.
It can be used on its own or blended with Seraseq Methylated ctDNA mutation mix to create a desired percent
methylated ctDNA profile.
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、生殖健康和遗传病。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