TheBovineLDBeadChipmicroarraykitenablesaccurategenotypingtounderstandtheimpactofgeneticsonmilkproduction,reproduction,health,andmore.Deliveringsuperior,scalablecontentataneconomicalprice,itallowsyoutoextendgenomicselectiontotheentireherd.Thisarrayoffers:
TheBovineLDv2.0BeadChip,togetherwiththeInfiniumBovineSNP50,InfiniumBovineHD,andiSelectCustomBeadChips,createsabroadgenotypingportfoliothatbreederscanrelyontocharacterizegeneticvariationandaccuratelyestimategenomicbreedingvalue.
WhiletheBovineHDandBovineSNP50BeadChipsprovidesuperiorpowertointerrogategeneticvariationinhigh-valueanimalsandsupportgenome-widestudies,theBovineLDv2.0BeadChipenablesthecost-effectivegenotypingoflower-valueanimals.
TheBeadChip’sstrategicallyselectedSNPspossessdemonstratedreliability,highaverageminorallelefrequency(MAF),uniformdistributionacrossthebovinegenome,andexcellentimputationperformanceforarangeofglobaldairybreeds.The7,931SNPsontheBovineLDv2.0BeadChipweresubjectedtorigorousfunctionaltestingonmultiplebreedstoensurestrongperformance.IlluminaensuresthateveryBovineLDBeadChipoffers>99%averagecallrateacrosscommondairyandbeefcattlebreeds.
IlluminadevelopedtheBovineLDv2.0BeadChipaspartofaBovineLDConsortiumincollaborationwithglobalbovineagriculturalthoughtleaders.IlluminascientistsandcollaboratorsreferencedhistoricaldatageneratedwiththeBovineSNP50BeadChiptoidentifythebestSNPcontentforimputationefficiencyamongglobaldairybreeds.1
InsilicotestingdeterminedthatthehighestimputationefficiencycouldbeachievedbyoptimizingMAFamongtargetedbreedsandevenlyspacingSNPsacrosstheentirebovinegenomewithhighermarkerdensitiesatthechromosomalends.Contentincludescoverageofallchromosomes,includingX,knownYhaplotypes,andmitochondrialDNA.
TheInfiniumAssaypowersthismulti-samplegenotypingpanel,deliveringtheindustry’shighestcallratesandreproducibility.Theassay’sPCR-freesingle-tubesamplepreparationsignificantlyreduceslaborandpotentialsamplehandlingerrors.2,3Amulti-sampleformatfurtherreducesexperimentalvariabilityandoverallprojectcostbyallowingbreederstointerrogateupto24samplesinparallel.
LearnMoreAboutPlantandAnimalGenotyping
InputQuantity | 200ngDNA(at50ng/ul) |
NumberofMarkers | Fixedmarkers:7931evenlyspacedSNPsacrossthegenomeu003cbru003eCustommarkeradd-oncapacity:Upto80,000(with+kitversions) |
Technology | Microarray |
SpeciesCategory | Bovine |
AutomationCapability | LiquidHandlingRobots,Autoloader2.xArrayLoader |
SystemCompatibility | iScan |
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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用于基因分型和表观遗传分析的微阵列试剂盒
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。