品牌分类
- Protein Expression|Protein Purification|Protein Tools
- DNA Modifying Enzymes and Cloning Technologies|Next Generation Sequencing Library Preparat
- DNA修饰酶
- DNA Assembly Cloning and Mutagenesis Kits
- DNA修饰酶和克隆技术|NGS样品制备&;目标富集|PCR
- 缓冲液|下一代测序文库制备|NGS样品制备&;目标富集
- Protein Expression|Protein Expression & Purification Technologies|Protein Purification
- 表观遗传学|限制性内切酶
- DNA Modifying Enzymes and Cloning Technologies|Epigenetics
- Nucleic Acid Purification|RNA Reagents
- 表观遗传学
- DNA Modifying Enzymes and Cloning Technologies
- Buffers|DNA Modifying Enzymes and Cloning Technologies|PCR, Polymerases & Amplificatio
- Buffers|Markers & Ladders|RNA Reagents
- Next Generation Sequencing Library Preparation|NGS Sample Prep & Target Enrichment
- Nucleic Acid Purification|Protein Expression & Purification Technologies|RNA Reagents
- Next Generation Sequencing Library Preparation|PCR, Polymerases & Amplification Techno
- Buffers|DNA Modifying Enzymes and Cloning Technologies
- Buffers|Competent Cells
- DNA Modifying Enzymes and Cloning Technologies|Next Generation Sequencing Library Preparat
- Next Generation Sequencing Library Preparation|PCR, Polymerases & Amplification Techno
品牌咨询
- 血管紧张素转换酶抑制剂治疗慢性心衰要用多大剂量
- 乳腺癌熬过五年就不复发?专家:七年也是小高峰_治疗
- 乳酸脱氢酶(LDH)释放法检测NK细胞活性实验资讯...
- 李嘉诚捐资千万助力CRISPR基因技术研究
- 利用CRISPR/Cas9系统可拯救失明小鼠—论文—
- New England Biolabs公司(NEB) 企业动态
- 利用CRISPR/Cas9系统可拯救失明小鼠中国科学院
- neb【中国试剂网】 neb|产品详情|
- NEB “星选聚惠”秋季促销
- 伯乐Biorad 1421253 Chelex 100 Resin, Chelex 100树脂,现货_价格...
- NEB_专业生化试剂网上商城 Solarbio.com
- 2011第二届工业酶与生物催化大会邀请函.doc
联系方式
公司地址
苏州工业园区生物纳米园A4#216
联系电话
4000-520-616 / 18915418616
传真号码
0512-67156496
电子邮箱
info@ebiomall.com
公司网址
https://www.ebiomall.com
商品描述
Description:
TheOneTaqOne-StepRT-PCRKitofferssensitiveandrobustend-pointdetectionofRNAtemplates.CDNAsynthesisandPCRamplificationstepsareperformedinasinglereactionusinggene-specificprimers,resultinginastreamlinedRT-PCRprotocol.Thekitcombinesthreeoptimizedmixes:OneTaqOne-StepEnzymeMix,OneTaqOne-StepReactionMixandOneTaqOne-StepQuick-LoadReactionMix.TheEnzymeMixcombinesProtoScriptIIReverseTranscriptase,MurineRNaseInhibitorandOneTaqHotStartDNAPolymerase.ProtoScriptIIReverseTranscriptaseisamutantM-MuLVreversetranscriptasewithreducedRNaseHactivityandincreasedThermostABIlity.OneTaqHotStartDNAPolymeraseismixtureofaHotStartTaqDNAPolymerasecombinedwithaproof-reADIngDNApolymerase,resultinginhigh-yieldamplificationwithminimaloptimization.TheOneTaqOne-StepRT-PCRKitiscapableofamplifyinglongtranscriptsupto9kbinlength.
Twooptimizedreactionmixesareincluded,OneTaqOne-StepReactionMixandQuick-LoadOneTaqOne-StepReactionMix.ThereactionmixesofferrobustconditionsforbothcDNAsynthesisandPCRamplification.TheuniqueOneTaqQuick-LoadOne-StepReactionMixcontainsadditionaldyes,offeringcolorindicationforreactionsetupaswellasdirectgelloading.
BothtotalRNAandmRNAcanbeusedastemplate.ThekitcandetectaGAPDHtargetaslowas0.1pgperreaction.ItcanroutinelydetectRNAtargetsupto9kb.TheOneTaqOne-StepRT-PCRKitiscapableofmultiplexdetectionoftwoorthreetargets.

About100ngofJurkattotalRNAwasusedin50μlreactionsfollowingthestandardprotocol.Thetargetsizes wereLane1:0.7kb,Lane2:1.1kb,Lane3:1.9kb,Lane4:2.3kb,Lane5:2.5kb,Lane6:5.5kb,Lane7:7.6kb andLane8:9.3kb.TheMarkerlane(M)containsQuick-Load2-logDNALadder(NEB#N0469).

SerialdilutionofHeLatotalRNA(Lane1:1μg,Lane2:100ng,Lane3:10ng,Lane4: 1ng,Lane5:100pg,Lane6:10pg,Lane7:1pg,Lane8:0.1pg)wasusedin50μl reactionsfollowingtheStandardProtocol.Themarkerlane(M)containsQuick-Load2-log DNALadder(NEB#N0469).
KitComponents
Thefollowingreagentsaresuppliedwiththisproduct:
| Storeat(°C) | Concentration | |
| OneTaqOne-StepEnzymeMix | -20 | |
| OneTaqOne-StepReactionMix | -20 | |
| Quick-Load®OneTaqOne-StepReactionMix | -20 | |
| Nuclease-freeWater | -20 |


