Ikhwalithi ephezulu yase-China Universal Blue Sybr Green Qpcr Master Mix ene-Yellow Template Dilution Buffer
Ukuthola ukwaneliseka kwabathengi kuyinhloso yenkampani yethu ngaphandle kokuphela.Sizokwenza imizamo emangalisayo yokukhiqiza okuthengiswayo okusha kanye nekhwalithi ephezulu, sanelise izidingo zakho ezikhethekile futhi sikunikeze ngezinkonzo ezidayiswa ngaphambili, ezithengiswayo kanye nangemva kokuthengisa Zekhwalithi Ephezulu I-China Universal Blue Sybr Green.I-Qpcr Master Mixnge-Yellow Template Dilution Buffer, Sihlose ukusungulwa kwesistimu eqhubekayo, ukusungula izinto ezintsha zokuphatha, ukuqanjwa kwekhethelo kanye nokuqanjwa kabusha kwemboni, sinikeza ukudlala ngokugcwele kuzo zonke izinzuzo, futhi siqhubeke senza ukuthuthukiswa ukuze kusetshenziswe izinga eliphezulu.
Ukuthola ukwaneliseka kwabathengi kuyinhloso yenkampani yethu ngaphandle kokuphela.Sizokwenza imizamo emangalisayo yokukhiqiza okuthengiswayo okusha kanye nekhwalithi ephezulu, ukwanelisa izidingo zakho ezikhethekile futhi sikunikeze ngezinsizakalo ezithengiswa ngaphambilini, ezithengiswayo kanye nangemuva kokuthengisa.I-China Qpcr Premix, I-Qpcr Master Mix, Iwebhusayithi yethu yasekhaya ikhiqiza ama-oda okuthenga angaphezu kuka-50, 000 njalo ngonyaka futhi iphumelela kakhulu ekuthengeni i-inthanethi e-Japan.Singajabula ukuthola ithuba lokwenza ibhizinisi nenkampani yakho.Sibheke ngabomvu ukuthola umlayezo wakho!
Izincazelo
Le khithi isebenzisa isistimu ye-lysis buffer eyingqayizivele engakhulula ngokushesha i-RNA kumasampula eseli akhulisiwe ukuze kusabela i-RT-qPCR, ngaleyo ndlela iqede inqubo yokuhlanza i-RNA edla isikhathi nekhandlayo.Isifanekiso se-RNA singatholakala ngemizuzu engu-7 nje.I-5×Direct RT Mix kanye ne-2×Direct qPCR Mix-SYBR ama-reagents anikezwe ikhithi angathola ngokushesha nangempumelelo imiphumela ye-PCR yobuningi besikhathi sangempela.
I-5×Direct RT Mix kanye ne-2×Direct qPCR Mix-SYBR inokubekezelela okuqinile kwe-inhibitor, futhi i-lysate yamasampuli ingasetshenziswa njengesifanekiso se-RT-qPCR ngokuqondile.Le khithi iqukethe i-RNA high-affinity Foregene reverse transcriptase, kanye ne-Hot D-Taq DNA polymerase, dNTPs, MgCl2, isigcinalwazi sokusabela, i-PCR optimizer nesiqinisi.
Imininingwane
200×20μl Rxns, 1000×20μl Rxns
Izingxenye zekhithi
Ingxenye I | Isivimbeli CL |
I-Foregene Protease Plus II | |
Isilondolozi se-ST | |
Ingxenye II | I-DNA Eraser |
5× Imiksi ye-RT eqondile | |
2× Direct qPCR Mix-SYBR | |
I-50 × I-ROX Reference Dye | |
RNase-Free ddH2O | |
Iziyalezo |
Izici&izinzuzo
■ Kulula futhi kusebenza ngempumelelo : Ngobuchwepheshe be-Cell Direct RT, amasampula e-RNA angatholwa ngemizuzu engu-7 nje.
■ Isidingo sesampula sincane, siphansi njengoba amaseli ayi-10 angahlolwa.
■ Ukuphuma okuphezulu: ikwazi ukubona ngokushesha i-RNA kumaseli akhiwe kumapuleti angu-384, 96, 24, 12, 6-wemithombo.
■ I-DNA Eraser ingasusa ngokushesha ama-genome akhululiwe, inciphise kakhulu umthelela emiphumeleni yokuhlola elandelayo.
■ Isistimu ye-RT ethuthukisiwe kanye ne-qPCR yenza ukuloba okuhlanekezela okuzinyathelo ezimbili kwe-RT-PCR kusebenze kahle futhi i-PCR icace kakhulu, futhi imelane kakhulu ne-RT-qPCR reaction inhibitors.
Isicelo sekhithi
Ububanzi bokusebenza: amaseli akhulisiwe.
- I-RNA ekhishwe ngesampula ye-lysis: isebenza kuphela kusifanekiso se-RT-qPCR sale kit.
- Ikhithi ingasetshenziselwa lezi zinhloso ezilandelayo: ukuhlaziywa kwesisho sofuzo, ukuqinisekiswa komphumela wokuthulisa ufuzo we-siRNA-mediated, ukuhlolwa kwezidakamizwa, njll.
Umdwebo
Isitoreji kanye Nempilo yeshelufu
Ingxenye I yale kit kufanele igcinwe ku-4℃;Ingxenye II kufanele igcinwe ku -20 ℃.
I-Foregene Protease Plus II kufanele igcinwe ku-4℃, ingafrizi ku -20℃.
I-Reagent 2×Direct qPCR Mix-SYBR kufanele igcinwe ku -20℃ ebumnyameni;uma isetshenziswa njalo, ingabuye igcinwe ku-4℃ ukuze igcinwe isikhathi esifushane (isetshenziswe ngaphakathi kwezinsuku eziyi-10).Ukuthola ukwaneliseka kwabathengi kuyinjongo yenkampani yethu ngaphandle kokuphela.Sizokwenza imizamo emangalisayo yokukhiqiza okuthengiswayo okusha kanye nekhwalithi ephezulu, sanelise izidingo zakho ezikhethekile futhi sikunikeze ngezinkonzo ezidayiswa ngaphambili, ezithengiswayo kanye nangemva kokuthengisa Zekhwalithi Ephezulu I-China Universal Blue Sybr Green.I-Qpcr Master Mixnge-Yellow Template Dilution Buffer, Sihlose ukusungulwa kwesistimu eqhubekayo, ukusungula izinto ezintsha zokuphatha, ukuqanjwa kwekhethelo kanye nokuqanjwa kabusha kwemboni, sinikeza ukudlala ngokugcwele kuzo zonke izinzuzo, futhi siqhubeke senza ukuthuthukiswa ukuze kusetshenziswe izinga eliphezulu.
Ikhwalithi ephezuluI-China Qpcr Premix, I-Qpcr Master Mix, Iwebhusayithi yethu yasekhaya ikhiqiza ama-oda okuthenga angaphezu kuka-50, 000 minyaka yonke futhi iphumelela kakhulu ekuthengeni i-inthanethi e-Japan.Singajabula ukuthola ithuba lokwenza ibhizinisi nenkampani yakho.Sibheke ngabomvu ukuthola umlayezo wakho!
Izimiso ze-Real Time PCR primer design
Dlulisela phambili i-Primer kanye ne-Primer Reverse
Nge-Real Time PCR, ukuklama kokuqala kubaluleke kakhulu.Ama-Primers ahlobene nokucaciswa nokusebenza kahle kokukhulisa i-PCR, futhi angaklanywa ngokubhekiselwa kule migomo elandelayo:
Ubude be-Primer: 18-30bp.
Okuqukethwe kwe-GC: 40-60%.
Inani le-Tm: Isofthiwe yokuklama i-Primer, njenge-Primer 5, inganikeza inani le-Tm le-primer.Amanani e-Tm okuqalisa akhuphuka nomfula kufanele abe seduze ngangokunokwenzeka.Ifomula yokubala ye-Tm nayo ingasetshenziswa: Tm = 4 °C (G + C) + 2 °C (A + T).Lapho kwenziwa i-PCR, izinga lokushisa elingaphansi kwenani lokuqala le-Tm elingu-5 °C livame ukukhethwa njengezinga lokushisa lokukhipha isisu (ukwenyuka okuhambisanayo kwezinga lokushisa le-anneal kungakhuphula ukucaciswa kokusabela kwe-PCR).
Ama-Primers kanye nemikhiqizo ye-PCR:
I-design primer PCR ubude bomkhiqizo wokukhulisa u-100-150bp.
Iziqalo zokuklama endaweni yesibili yesakhiwo sesifanekiso kufanele zigwenywe kakhulu ngangokunokwenzeka.
Gwema ukwakheka kwezisekelo ezi-2 noma ngaphezulu ezihambisanayo phakathi kwamaphethelo angu-3′ weziqalisi ezikhuphuka nomfula.
Isisekelo setheminali ye-Primer 3′ asikwazi ukuba khona nezinye ezingu-3 ezengeziwe ezilandelanayo ze-G noma C.
Ama-primer ngokwawo awakwazi ukuba nezakhiwo ezihambisanayo, ngaphandle kwalokho kuzokwakhiwa isakhiwo se-hairpin, esithinta ukukhuliswa kwe-PCR.
I-ATCG kufanele isatshalaliswe ngokulinganayo ngangokunokwenzeka ekulandeleni kokuqala, futhi isisekelo setheminali esingu-3′ kufanele sigwenywe njengo-T.
Isithasiselo 1:Iphakethe lengxenye ye-Cell Direct RT-qPCR Kit
1.Cell Lysis Solution
| |||
Izingxenye zekhithi (Isistimu ye-lysis ye-24 / kahle) | I-DRT-01011-A1 | I-DRT-01011-A2 | |
100 T | 500 T | ||
IngxenyeI | Isivimbeli CL | 20 ml | 100 ml |
I-Foregene Protease Plus II | 400 μl | 1 ml × 2 | |
Isilondolozi se-ST | 1 ml × 2 | 10 ml | |
IngxenyeII | I-DNA Eraser | 400 μl | 1 ml × 2 |
2.RT Imiksi
| |
Izingxenye zekhithi (Isistimu yokusabela engu-20 μl) | I-DRT-01011-B1 |
200 T | |
5× Imiksi ye-RT eqondile | 800 μl |
I-ddH yamahhala ye-RNase2O | 1.7 ml × 2 |
| ||
Izingxenye zekhithi (Isistimu yokusabela engu-20 μl) | I-DRT-01011-C1 | I-DRT-01011-C2 |
200 T | 1000 T | |
2× Direct qPCR Mix-SYBR | 1 ml × 2 | 1.7 ml × 6 |
I-50 × I-ROX Reference Dye | 40 ml | 200 μl |
I-ddH yamahhala ye-RNase2O | 1.7 ml | 10 ml |