Izitolo zefekthri ze-China High Efficiency PCR, i-Taq Plus DNA Polymerase
Sinalesi siqubulo, sesiphenduke omunye wabakhiqizi okungenzeka ukuthi bathuthuke kakhulu, abangabizi kakhulu, futhi abancintisana namanani efekthri Izitolo ze-China High Efficiency PCR, i-Taq Plus DNA Polymerase, Enkampanini yethu enekhwalithi ephezulu esizoqala ngayo njengesiqubulo sethu, senza imikhiqizo eyenziwe e-Japan ngokuphelele, kusukela ekuthengeni izinto zokwakha.Lokhu kubenza bakwazi ukuzisebenzisa ngokuthula kwengqondo.
Sinalesi siqubulo engqondweni, sesiphenduke omunye wabakhiqizi okungenzeka ukuthi baqambe kakhulu, ababiza kakhulu, nabancintisana namanani entengo.I-China PCR Amplification, Qpcr, Ubungcweti, Ukuzinikela kuhlale kubalulekile emsebenzini wethu.Besilokhu sihambisana nokusebenzela amakhasimende, sakha izinhloso zokuphathwa kwevelu futhi sihambisana nobuqotho, ukuzinikela, nombono wokuphatha oqhubekayo.
Imininingwane
50×20μl rxns, 200×20μl rxns, 1000×20μl rxns, 2000×20μl rxns
I-2X Real PCR EasyTM Mix-Taqman ehlinzekwa yi-Real Time PCR EasyTM-Taqman kit iwuhlelo olusha lwe-premix olusebenzisa ama-fluorescent probes athile okusabela kokukhulisa i-Real Time PCR, okungathuthukisa kakhulu ukucaciswa komkhiqizo nokuzwela kokusabela.I-ROX inikezwa njengodayi wokulawula wangaphakathi.
I-2X Real PCR EasyTM Mix-Taqman iqukethe i-Taq DNA Polymerase eyingqayizivele ye-Foregene.Uma iqhathaniswa nama-enzyme e-Taq ajwayelekile, inezinzuzo zokusebenza kahle kokukhulisa i-amplification, ikhono elithile eliqinile lokukhulisa kanye nezinga lokungafani eliphansi.Inganciphisa ukukhulisa okungaqondile futhi ithuthukise ukunemba kwe-PCR.
Izingxenye zekhithi
I-2 × I-PCR yangempela kululaTM I-Mix-Taqman |
I-20 × I-ROX Reference Dye |
I-DNase-Free ddH2O |
Iziyalezo |
Izici&izinzuzo
■ I-Simple—2X PCR Mix ukuze kwehliswe iphutha lokuhlola nesikhathi sokusebenza
■ Ibhafa ecacisiwe—elungiselelwe kahle kanye ne-enzyme ye-Taq eqala ukushisa ingavimbela ukukhulisa okungaqondile kanye nokwakheka kwe-primer dimer.
■ Ukuzwela okuphezulu—kukwazi ukubona amakhophi aphansi esifanekiso
■ Ukuguquguquka okuhle—kuhambisana nezinsimbi eziningi zesikhathi sangempela ze-PCR
Isicelo sekhithi
Ukuhlaziywa kwe-qPCR
Ukugeleza komsebenzi
Umfanekiso
Isitoreji kanye Nempilo yeshelufu
Le kit kufanele igcinwe kude nokukhanya futhi kufanele igcinwe ku -20 ℃.Uma isetshenziswa njalo, ingabuye igcinwe ku-4℃ isikhathi esifushane (izinsuku eziyi-10).Sinalesi siqubulo engqondweni, sesiguquke saba omunye wabakhiqizi okungenzeka kakhulu, abangabizi kakhulu, nabancintisanayo ngentengo ye-Factory Outlets for China High Efficiency PCR, Taq Plus DNA Polymerase, to 25u2 yethu abakhiqizi bezinga eliphezulu, kuya ku-2503 yethu yokuqala nge-DNA yethu njenge-motto 2. imikhiqizo eyenziwe ngokuphelele e-Japan, kusukela ekuthengeni izinto zokwakha kuye ekucutshungulweni.Lokhu kubenza bakwazi ukuzisebenzisa ngokuthula kwengqondo.
Izitolo zemboni zeI-China PCR Amplification, Qpcr, Ubungcweti, Ukuzinikela kuhlale kubalulekile emsebenzini wethu.Besilokhu sihambisana nokusebenzela amakhasimende, sakha izinhloso zokuphathwa kwevelu futhi sihambisana nobuqotho, ukuzinikela, nombono wokuphatha oqhubekayo.
Awekho amasiginali wokukhulisa umsindo
1.I-Taq DNA Polymerase kukhithi ilahlekelwa umsebenzi wayo ngenxa yokugcinwa okungalungile noma ukuphelelwa yisikhathi kwekhithi.
Okutuswayo: Qinisekisa izimo zokugcinwa kwekhithi;wengeze kabusha inani elifanele le-Taq DNA Polymerase ohlelweni lwe-PCR noma uthenge Ikhithi ye-PCR Yesikhathi Sangempela entsha ngokuhlolwa okuhlobene.
2.Kunenqwaba yama-inhibitors e-Taq DNA Polymerase kusifanekiso se-DNA.
Isiphakamiso: Hlanza kabusha isifanekiso noma wehlise inani lesifanekiso esisetshenzisiwe.
3.I-Mg2+ concentration ayifanele.
Isincomo: Ukugxiliswa kwe-Mg2+ kwe-2× Real PCR Mix esikunikezayo ngu-3.5mM.Kodwa-ke, kwezinye iziqalo ezikhethekile nezifanekiso, ukugxila kwe-Mg2+ kungase kube phezulu.Ngakho-ke, ungakwazi ukwengeza i-MgCl2 ngokuqondile ukuze uthuthukise ukugxila kwe-Mg2+.Kunconywa ukuthi ukhuphule i-Mg2+ 0.5mM isikhathi ngasinye ukuze kuthuthukiswe.
I-4.Izimo zokukhulisa i-PCR azifaneleki, futhi ukulandelana kwe-primer noma ukugxila akufanelekile.
Isiphakamiso: qinisekisa ukunemba kokulandelana kwe-primer futhi i-primer ayizange yehliswe;uma isignali yokukhulisa i-amplification ingalungile, zama ukwehlisa izinga lokushisa le-anneal futhi ulungise ukugxila kwe-primer ngendlela efanele.
5.Inani lesifanekiso lincane kakhulu noma liningi kakhulu.
Okunconyiwe: Yenza isifanekiso sokuhlanjululwa kwe-gradient yomugqa, bese ukhetha ukugxiliswa kwesifanekiso esinomphumela we-PCR ongcono kakhulu wokuhlolwa kwe-PCR ye-Real Time.
I-NTC inevelu ye-fluorescence ephezulu kakhulu
Ukungcola kwe-1.Reagent okubangelwa ngesikhathi sokusebenza.
Okunconyiwe: Faka esikhundleni ngama-reagents amasha okuhlolwa kwe-PCR ye-Real Time.
2.Ukungcola kwenzeke ngesikhathi sokulungiswa kohlelo lokusabela kwe-PCR.
Okunconyiwe: Thatha izinyathelo zokuzivikela ezidingekayo ngesikhathi sokusebenza, njengokuthi: ukugqoka amagilavu e-latex, ukusebenzisa ithiphu ye-pipette ngesihlungi, njll.
3.Iziqalo zehlisiwe, futhi ukucekelwa phansi kweziqalo kuzodala ukukhuliswa okungaqondile.
Isiphakamiso: Sebenzisa i-SDS-PAGE electrophoresis ukuze uthole ukuthi iziqalo zonakalisiwe, futhi esikhundleni sazo ufake iziqalisi ezintsha zokuhlolwa kwe-PCR ye-Real Time.
I-Primer dimer noma ukukhulisa okungaqondile
1.I-Mg2+ concentration ayifanele.
Okutuswayo: Ukugxiliswa kwe-Mg2+ ye-2× Real PCR EasyTM Mix esiyinikezayo ngu-3.5 mM.Kodwa-ke, kwezinye iziqalo ezikhethekile nezifanekiso, ukugxila kwe-Mg2+ kungase kube phezulu.Ngakho-ke, ungakwazi ukwengeza i-MgCl2 ngokuqondile ukuze uthuthukise ukugxila kwe-Mg2+.Kunconywa ukuthi ukhuphule i-Mg2+ 0.5mM isikhathi ngasinye ukuze kuthuthukiswe.
2.Izinga lokushisa le-PCR annealing liphansi kakhulu.
Isiphakamiso: Nyusa izinga lokushisa le-PCR le-anneal ngo-1℃ noma ngo-2℃ isikhathi ngasinye.
3.Umkhiqizo we-PCR mude kakhulu.
Okunconyiwe: Ubude bomkhiqizo we-Real Time PCR kufanele bube phakathi kuka-100-150bp, bungabi ngaphezu kuka-500bp.
I-4.Ama-primers awonakala, futhi ukuchithwa kwama-primers kuzoholela ekubukeni kokukhulisa okuqondile.
Isiphakamiso: Sebenzisa i-SDS-PAGE electrophoresis ukuze uthole ukuthi iziqalo zonakalisiwe, futhi esikhundleni sazo ufake iziqalisi ezintsha zokuhlolwa kwe-PCR ye-Real Time.
5.Isistimu ye-PCR ayilungile, noma isistimu incane kakhulu.
Isiphakamiso: Isistimu yokusabela ye-PCR incane kakhulu izobangela ukunemba kokutholwa kwehle.Kungcono kakhulu ukusebenzisa isistimu yokusabela enconywe ithuluzi le-PCR lobuningi ukuze uqalise kabusha ukuhlolwa kwe-PCR ye-Real Time.
Ukuphindaphinda okubuthakathaka kwamanani omthamo
1.Ithuluzi alisebenzi kahle.
Isiphakamiso: Kungase kube namaphutha phakathi kwembobo ngayinye ye-PCR yethuluzi, okuholela ekukhiqizeni kabusha okubi ngesikhathi sokuphathwa kwezinga lokushisa noma ukutholwa.Sicela uhlole ngokulandela imiyalelo yethuluzi elihambisanayo.
2.Ukuhlanzeka kwesampula akukuhle.
Okunconyiwe: Amasampuli angcolile azoholela ekukhiqizeni kabusha okubi kokuhlolwa, okufaka ukuhlanzeka kwesifanekiso nama-primers.Kungcono ukuhlanza kabusha isifanekiso, futhi ama-primer ahlanzwa kangcono yi-SDS-PAGE.
3.Ukulungiswa kohlelo lwe-PCR nesikhathi sokugcina side kakhulu.
Isiphakamiso: Sebenzisa isistimu ye-PCR ye-Real Time yesilingo se-PCR ngokushesha ngemva kokulungiselela, futhi ungayishiyi eceleni isikhathi eside kakhulu.
I-4.Izimo zokukhulisa i-PCR azifaneleki, futhi ukulandelana kwe-primer noma ukugxila akufanelekile.
Isiphakamiso: qinisekisa ukunemba kokulandelana kwe-primer futhi i-primer ayizange yehliswe;uma isignali yokukhulisa i-amplification ingalungile, zama ukwehlisa izinga lokushisa le-anneal futhi ulungise ukugxila kwe-primer ngendlela efanele.
5.Isistimu ye-PCR ayilungile, noma isistimu incane kakhulu.
Isiphakamiso: Isistimu yokusabela ye-PCR incane kakhulu izobangela ukunemba kokutholwa kwehle.Kungcono kakhulu ukusebenzisa isistimu yokusabela enconywe ithuluzi le-PCR lobuningi ukuze uqalise kabusha ukuhlolwa kwe-PCR ye-Real Time.