I-MOQ ephansi ye-Magpure Ffpe Rna Kit ye-Nucleic Acid Isolation & Purification Kit
Enesimo sengqondo esihle nesinenqubekelaphambili ekuthakaseleni kwamakhasimende, ibhizinisi lethu lihlala lithuthukisa into yethu ngendlela enhle kakhulu ukwanelisa izifiso zamakhasimende futhi ligxile kakhulu kwezokuphepha, ukwethembeka, izimfuno zemvelo, kanye nokuqanjwa okusha kwe-MOQ ephansi ye-Magpure Ffpe Rna Kit ye-Nucleic Acid Isolation & Purification Kit, Kuphela ngokufeza isixazululo sekhwalithi enhle nesidingo samakhasimende ngaphambi kokufeza isixazululo esiqinile semikhiqizo yamakhasimende.
Enesimo sengqondo esihle nesinenqubekela phambili ekuthatheni kwakhe amakhasimende, ibhizinisi lethu lihlala lithuthukisa into yethu ngendlela enhle kakhulu ukuze lanelise izifiso zamakhasimende futhi ligxile kakhulu ekuphepheni, ekuthembekeni, ekufuneni imvelo, nasekusunguleni izinto ezintsha.Uhlelo lwe-China Nucleic Acid Extraction kanye ne-Nucleic Acid Isolation, Inkampani yethu inamathela esimisweni "sekhwalithi ephezulu, intengo enengqondo kanye nokulethwa okufika ngesikhathi".Sithemba ngobuqotho ukusungula ubudlelwano obuhle bokusebenzisana nozakwethu abasha nabakudala bebhizinisi abavela kuzo zonke izingxenye zomhlaba.Sithemba ukusebenza nawe futhi sikukhonze ngemikhiqizo namasevisi ethu amahle kakhulu.Siyakwamukela ukusijoyina!
Amamanuwali wemiyalo:
Enesimo sengqondo esihle nesinenqubekelaphambili ekuthakaseleni kwamakhasimende, ibhizinisi lethu lihlala lithuthukisa into yethu ngendlela enhle kakhulu ukwanelisa izifiso zamakhasimende futhi ligxile kakhulu kwezokuphepha, ukwethembeka, izimfuno zemvelo, kanye nokuqanjwa okusha kwe-MOQ ephansi ye-Magpure Ffpe Rna Kit ye-Nucleic Acid Isolation & Purification Kit, Kuphela ngokufeza isixazululo sekhwalithi enhle nesidingo samakhasimende ngaphambi kokufeza isixazululo esiqinile semikhiqizo yamakhasimende.
I-MOQ ephansi yeUhlelo lwe-China Nucleic Acid Extraction kanye ne-Nucleic Acid Isolation, Inkampani yethu inamathela esimisweni "sekhwalithi ephezulu, intengo enengqondo kanye nokulethwa okufika ngesikhathi".Sithemba ngobuqotho ukusungula ubudlelwano obuhle bokusebenzisana nozakwethu abasha nabakudala bebhizinisi abavela kuzo zonke izingxenye zomhlaba.Sithemba ukusebenza nawe futhi sikukhonze ngemikhiqizo namasevisi ethu amahle kakhulu.Siyakwamukela ukusijoyina!
Umhlahlandlela Wokuhlaziya Inkinga
Okulandelayo ukuhlaziya izinkinga ezingase kuhlangatshezwane nazo ekukhishweni kwe-viral DNA/RNA, ngethemba lokuba usizo ekuhloleni kwakho.Ngaphezu kwalokho, kwezinye izinkinga zokuhlola noma zobuchwepheshe ngaphandle kwemiyalo yokusebenza nokuhlaziya inkinga, sinikele ngosekelo lobuchwepheshe ukuze sikusize.Uma unezinye izidingo, sicela usithinte: 028-83360257 noma E-mail:
Tech@foregene.com.
Akukho ukukhishwa kwe-nucleic acid noma isivuno esiphansi se-nucleic acid
Ngokuvamile kuba nezinto eziningi ezithinta ukusebenza kahle kokululama, njengalezi: isampula yokuqukethwe kwe-nucleic acid, indlela yokusebenza, ivolumu ye-elution, njll.
Ukuhlaziywa kwezimbangela ezijwayelekile:
1. Ukugeza kweqhwa noma izinga lokushisa eliphansi (4 ° C) i-centrifugation yenziwa ngesikhathi senqubo.
Ukusikisela: Sebenzisa ekamelweni lokushisa (15-25°C) kuyo yonke inqubo, ungabhavi eqhweni kanye nokushisa okuphansi kwe-centrifugation.
2. Isampula ligcinwe ngendlela engafanele noma isampula ligcinwe isikhathi eside kakhulu.
Okutuswayo: Gcina amasampula ku -80°C futhi ugweme ukuqhwa okuphindaphindiwe nokuncibilika;zama ukusebenzisa amasampula asanda kuqoqwa ukuze kukhishwe i-nucleic acid.
3. Isampula yesampula enganele.
Okutuswayo: Sicela uqinisekise ukuthi isampula kanye nesisombululo sokusebenza se-lysis kuxutshwe kahle futhi kufakwe endaweni yokushisa yegumbi (15-25°C) imizuzu eyi-10.
4. Ukwengezwa okungalungile kwe-eluent.
Isiphakamiso: Qiniseka ukuthi i-ddH2O Engenayo i-RNase yengezwa ngokudonsela phansi maphakathi nolwelwesi lwekholomu yokuhlanza, futhi ungayibeki eringini yekholomu yokuhlanza.
5. Ivolumu elungile ye-ethanol ephelele ayizange yengezwe ku-Buffer RW2.
Ukusikisela: Sicela ulandele imiyalelo, wengeze ivolumu efanele ye-ethanol ephelele ku-Buffer RW2 futhi uhlanganise kahle ngaphambi kokusebenzisa ikhithi.
6. Ivolumu yesampula engafanele.
Isiphakamiso: U-200µl wesampula ucutshungulwa kuwo wonke u-500µl we-Buffer DRL.Ukucutshungulwa kwesampula okweqile kuzoholela emvuzweni ephansi yokukhipha i-nucleic acid.
7. Ivolumu ye-elution engafanele noma ukungezwani okuphelele.
Isincomo: Ivolumu ecacile yekholomu yokuhlanza ingu-30-50μl;uma umphumela we-elution ungagculisi, kuyanconywa ukuthi unwebe isikhathi kuzinga lokushisa legumbi ngemva kokwengeza i-ddH2O eshisiwe ye-RNase-Free, njenge-5-10min.
8. I-Ethanol ihlala kukholamu ngemva kokugeza nge-Buffer RW2.
Isiphakamiso: Uma i-ethanol isala ngemva kokufakwa phakathi kwe-centrifugation ne-Buffer RW2 imizuzu emi-2, ikholomu ingabekwa ekamelweni lokushisa imizuzu emi-5 ngemva kwe-centrifugation ukuze ikhiphe ngokuphelele i-ethanol esele.
I-nucleic acid ehlanzekile iyancipha
Izinga le-nucleic acid ehlanzekile lihlobene nokulondolozwa kwesampula, ukungcoliswa kwe-RNase, ukusebenza nezinye izici.Ukuhlaziywa kwezimbangela ezijwayelekile:
1. Amasampula aqoqiwe awagcinwanga ngesikhathi.
Ukusikisela: Uma isampuli ingasetshenziswa ngesikhathi ngemva kokuqoqwa, sicela uyigcine ku -80°C ezingeni lokushisa eliphansi ngokushesha.Ukuze uthole i-RNA, zama ukusebenzisa amasampuli asanda kuqoqwa.
2. Qoqa amasampula bese uwaqandisa futhi uncibilike ngokuphindaphindiwe.
Ukusikisela: Gwema ukuqanda nokuncibilika (hhayi ngaphezu kokukodwa) ngesikhathi sokuqoqwa nokugcinwa kwamasampula, ngaphandle kwalokho isivuno se-nucleic acid sizoncipha.
3. I-RNase yethulwa egumbini lokuhlinza noma amagilavu alahlwayo, imaski, njll. awagqokwa.
Okutuswayo: Ukuhlolwa kokukhipha i-RNA kwenziwa kangcono kakhulu ekamelweni lokusebenza elihlukile le-RNA, futhi itafula laselabhorethri kufanele lihlanzwe ngaphambi kokuhlolwa.
Gqoka amagilavu alahlwayo namamaski ngesikhathi sokuhlolwa ukuze ugweme ukucekelwa phansi kwe-RNA okubangelwa ukwethulwa kwe-RNase ngezinga elikhulu kakhulu.
4. I-reagent yonakaliswe i-RNase ngesikhathi sokusetshenziswa.
Isincomo: Faka esikhundleni se-Viral DNA/RNA Isolation Kit entsha ukuze uthole ukuhlolwa okuhlobene.
5. Amashubhu e-centrifuge namathiphu e-piette asetshenziselwa ukukhwabanisa kwe-RNA angcoliswe yi-RNase.
Ukusikisela: Qinisekisa ukuthi amashubhu e-centrifuge, amathiphu e-pipette, amapayipi, njll. asetshenziselwa ukukhipha i-RNA konke Akuna-RNAse.
I-nucleic acid ehlanjululwe ithinta ukuhlolwa okungezansi komfula
I-DNA ne-RNA ehlanjululwe yikholomu yokuhlanza, uma i-ion kasawoti kanye nokuqukethwe kwamaprotheni kuphezulu kakhulu, kuzothinta ukuhlolwa okuya phansi komfula, okufana nalokhu: Ukukhulisa i-PCR, ukuloba okuhlanekezelwe, njll.
1. I-DNA ekhishiwe kanye ne-RNA inama-ion kasawoti asele.
Isiphakamiso: Qinisekisa ukuthi ivolumu elungile ye-ethanol ephelele yengezwa ku-Buffer RW2, futhi ugeze ikholomu yokuhlanza kabili ngesivinini sokuhlanganisa esishiwo emiyalweni yokusebenza;Yenza i-centrifugation ukuze unciphise ukungcoliswa kwe-ion kasawoti.
2. I-DNA ekhishiwe kanye ne-RNA inezinsalela ze-ethanol.
Ukusikisela: Ngemva kokuqinisekisa ukugeza nge-Buffer RW2, yenza i-tube centrifugation engenalutho ngesivinini se-centrifugation emiyalweni yokusebenza;uma kusekhona izinsalela ze-ethanol, ungakwazi ukufaka i-centrifuge ishubhu elingenalutho bese ulibeka endaweni yokushisa yasekamelweni imizuzu engu-5 ukuze ususe insalela ye-ethanol ngezinga elikhulu kakhulu.
Amamanuwali wemiyalo:
I-Viral DNA&RNA Isolation Kit Instruction Manual