请使用支持JavaScript的浏览器!
主营:基因芯片、二代测序NGS测序仪及相关测序试剂盒
banner
当前位置: 首页 > 产品中心 > Cluster Generation & Sequencing Reagents > Illumina/HiSeq PE Rapid Cluster Kit v2/PE-402-4002/1 Ea

Illumina/HiSeq PE Rapid Cluster Kit v2/PE-402-4002/1 Ea

Illumina/HiSeq PE Rapid Cluster Kit v2/PE-402-4002/1 Ea
  • Illumina/HiSeq PE Rapid Cluster Kit v2/PE-402-4002/1 Ea
商品介绍

ProductHighlights:

HiSeqRapidClusterKitsv2enabletheuniqueon-boardclustergenerationprocess.HiSeqRapidClusterKitsv2aredesignedtobeusedintherapidrunmodeofHiSeq2500and1500sequencers.

  • Optimizeyourworkflowwithon-boardclustergeneration
  • Improveturnaroundtimeandbatchingefficiency
  • Maximizethedataqualityofyourruns

Chooseon-boardclustergenerationtooptimizeyourworkflow–On-boardclustergenerationisauniquehigh-throughputworkflowoptionenabledbyHiSeqRapidClusterKitsv2,andisonlyavailableintherapidrunmodeoftheHiSeq2500or1500.

ClonaltemplateclustersaregeneratedfromindividualtemplatestrandsdirectlyontheHiSeq2500and1500instrumentusingthisprocess.On-boardclustergenerationminimizeshands-ontimeandenablesatruewalkawaysolution forhigh-throughputsequencingneeds.

Turnsamplesaroundfaster–HiSeqRapidClusterKitsv2supporttherapidrunworkflowfortheHiSeq2500and1500,andallowyoutoturnurgentsamplesaroundfaster.

Theloweroveralldatathroughputofrapidrunmodealsosimplifiesbatchingrequirementsandallowsoptimalindexingofsmallgenomesandotherapplicationswithreducedoutputneeds.

Maximizedataquality–HiSeqRapidClusterKitsv2arespecificallyformulatedtoworkwithHiSeqRapidSBSKitsv2andprovidethehighestqualitysequencingdataavailableonanyhigh-throughputsequencingsystem.

HiSeqRapidClusterKitsv2improveclusterdensityrobustnesstoincreasetotalusableclustersinagivenrunanddecreaseclustergrADIentsdownthelane.ThisincreasedrobustnessanduniformitycontributetohigherQ-scores,lowererrorrates,andhigherdataquality.

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



蚂蚁淘(ebiomall)作为一家生命科学领域的垂直电商平台,公司专注生物医学科研用品的全球导购和品牌推广,为海内外厂方与代理经销商搭建跨境贸易系统和交流平台。产品齐全,200+分类,1000+品牌,500万+产品信息。100%正品,专业售后,到货快,在线下单, 简单轻松,节省科学家宝贵的科研时间。为您竭诚服务!

【订购】蚂蚁淘生物科技  联系方式:4000-520-616

更多产品,更多优惠!请联系我们!

苏州蚂蚁淘生物科技有限公司

免费热线:4000-520-616

官网:https://www.ebiomall.cn/



  用于基因分型和表观遗传分析的微阵列试剂盒

产品信息图

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。

产品信息图

BovineLD基因分型珠芯片

该专家设计的基因分型阵列以经济的价格提供可扩展的内容,从而将基因组选择扩展到整个种群。

产品信息图

BovineSNP50 v3 DNA分析BeadChip

该BeadChip微阵列为主要奶牛和肉牛品种类型的基因组表征提供了高密度的多样品牛基因分型。

产品信息图

CanineHD全基因组基因分型珠芯片

该阵列可进行任何家犬品种的基因分型,并为品种内关联和CNV研究提供足够的SNP密度。

产品信息图

GGP牛和牛标志阵列

使用GeneSeek Genomic Profiler(GGP)牛微阵列准确预测关键特征,例如大理石花纹和肋眼区域。

产品信息图

GGP马阵列

选择所需的品种性状,并使用GeneSeek Genomic Profiler(GGP)马微阵列验证动物谱系。

产品信息图

GGP鼠标(GIGA-MUGA)阵列

GeneSeek Genomic Profiler(GGP)小鼠基因分型微阵列可实现标记辅助的选择和亲本应用。

产品信息图

GGP猪阵列

使用GeneSeek Genomic Profiler(GGP)猪微阵列靶向所需的育种特性和遗传组成,包括疾病易感性。

产品信息图

GGP土豆片

使用GeneSeek Genomic Profiler(GGP)马铃薯微阵列鉴定具有最大覆盖率的抗性区域。

产品信息图

HumanCytoSNP FFPE-12珠芯片

该BeadChip阵列针对使用福尔马林固定石蜡包埋(FFPE)配对的肿瘤正常样品的细胞遗传学研究进行了优化。

产品信息图

HumanCytoSNP-12珠芯片

这个由12个样本组成的BeadChip阵列可以分析人类基因组中的遗传和结构变异,例如重复,缺失,扩增,复制中性LOH和镶嵌。

产品信息图

Infinium亚洲筛选Array-24 v1.0 BeadChip

一个功能强大且经济高效的基因分型阵列,可用于东亚人群的大规模遗传研究和药物基因组学。

产品信息图

Infinium Core-24套件

这些阵列支持经济的大规模人类基因分型研究,具有高通量功能,并且可以添加多达300K的半定制标记。


自营商城图标
厂家直采
全球直采模式 正品优价
正品保障图标
正品保障
厂家直发 有线跟踪
解放采购图标
正规清关
CIF100%正规报关,提供发票
及时交付图标
及时交付
限时必达 不达必赔
在线客服
客服电话

4000-520-616

0512-67156496