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Illumina/Infinium Omni2.5-8 v1.3 Kit (48 samples) 2.5%) for diverse world populations. Each BeadChip can process 8 sampl

Illumina/Infinium Omni2.5-8 v1.3 Kit (48 samples) 2.5%) for diverse world populations. Each BeadChip can process 8 sampl
  • Illumina/Infinium Omni2.5-8 v1.3 Kit (48 samples) 2.5%) for diverse world populations. Each BeadChip can process 8 sampl
商品介绍

Product Highlights:

The Infinium Omni2.5-8 BeadChip offers an optimal and comprehensive set of both common and rare SNP content from the 1000 Genomes Project (MAF>2.5%) for diverse world populations. Using the proven iScan System, this 8-sample BeadChip offers not only high throughput, but optimized tag SNP content from 1000 Genomes Project pilot data.

With high data quality and cutting edge content, including full support of copy number variation (CNV) applications, this powerful genotyping tool allows you to make meaningful discoveries. For greater flexibility, the Infinium Omni2.5-8+ version of the BeadChip can be customized to include up to 200,000 additional markers.

Learn More About Human Genotyping

Specifications:

Number of MarkersFixed markers: 2,338,671,Custom marker add-on capacity: Up to 200,000
Sample Throughput~1067 samples per week
Input Quantity200 ng DNA
TechnologyMicroarray
Variant ClassSingle Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs)
Specialized Sample TypesFFPE
Species CategoryHuman
Automation CapabilityLiquid Handling Robots,Autoloader 2.x Array Loader
System CompatibilityiScan
品牌介绍

Illumina公司,致力于新一代测序和芯片技术的生产与开发,提供最新的产品与应用资讯。Illumina公司创立于1998年4月,是遗传变异和生物学功能分析领域的优秀的产品、技术和服务供应商。通过帮助客户加快实现生物信息的采集、分析和应用,来改善人类健康。

As a startup, Illumina aspired to transform human health. Our initial products enabled researchers to explore DNA at an entirely new scale, helping them create the first map of gene variations associated with health, disease, and drug response. Every breakthrough opened up a new world, and showed us how much further there is to go

While the rate of progress is accelerating exponentially, we are only beginning to understand the clinical significance of the genome. What causes a cancer cell to mutate? What is the origin of a puzzling disease? Is it possible to prevent the next outbreak? Or safeguard the world’s food supply? These are just a few of the challenges that inspire us to push the boundaries of our imagination

Today we are a global leader in genomics – an industry at the intersection of biology and technology. At the most fundamental level, we enable our customers to read and understand genetic variations. We strive to make our solutions increasingly simple, more accessible, and always reliable. As a result, discoveries that were unimaginable even a few years ago are now becoming routine – and are making their way into patient treatment.

We now have the ability to sequence at an unprecedented scale. Collectively, this will give us a much deeper understanding of genetics than ever before. We will begin to truly unlock the power of the genome. These advances will trigger a fundamental shift in healthcare and beyond. Medicine will continue to become more preventive and more precise. We will be healthier, longer. We have only just begun.

At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics



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Illumina-BovineHD DNA分析试剂盒

这个全面的全基因组牛基因分型阵列试剂盒具有超过777,000个SNP,可与任何种类的牛肉或奶牛兼容。

产品亮点

BovineHD BeadChip是一个全面的全基因组牛基因分型阵列,可用于询问任何牛肉和奶牛品种的遗传变异。Illumina与包括USDA-ARS,UNCEIA-INRA,辉瑞动物遗传学和密苏里大学在内的主要牛农业思想领袖合作开发了该产品。

该BeadChip具有超过777,000个SNP,它们均匀地分布在整个牛基因组中,可实现广泛的应用,例如全基因组选择,鉴定数量性状位点,评估遗传优势,杂交育种,连锁不平衡研究,比较遗传研究和品种鉴定以评估生物多样性。

八样本的BovineHD BeadChip以及经过验证的Infinium HD分析法为牛的全基因组研究提供了强大的高通量解决方案。

777,000 SNP BovineHD BeadChip支持全基因组范围内的全面基因分型研究,扩展了在遗传预测中评估的牛品种的多样性,并使更多的定量性状得以发现。

技术指标

输入数量200 ng DNA(50 ng / ul)
标记数固定标记:777,962个在基因组中均匀分布的SNPs
自定义标记附加能力:无
分析类型Infinium HD Super
方法全基因组基因分型阵列
自动化能力自动阵列装载机,液体处理机器人
系统相容性扫描仪
种类类别牛的
技术微阵列
特殊样品类型FFPE纸巾
核酸类型脱氧核糖核酸


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