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I-Fast Nucleic Acid Extraction Kit ye-Microbial kwi-Food

Inkcazelo yeKit:

Ikati.No.TK101

 

 

Le kit ithatha inkqubo yesisombululo esisodwa, esilula kwaye silungele ngaphandle kokutsalwa kunye nokucocwa, kwaye ingasetyenziselwa ngokuthe ngqo ukufumanisa i-nucleic acid amplification.

amandla angaphambili


Iinkcukacha zeMveliso

Iithegi zeMveliso

FAQ

KHUPHELA IZIXHOBO

Iinkcazelo

Le kit ithatha inkqubo yesisombululo esisodwa, esilula kwaye silungele ngaphandle kokutsalwa kunye nokucocwa, kwaye ingasetyenziselwa ngokuthe ngqo ukufumanisa i-nucleic acid amplification.

Imixholo yeKit

Igama

Compostion

Inkcazo

I-Agent yokuKhupha i-Nucleic Acid

Lysate

6mL

Usetyenziso olulindelekileyo

Isetyenziselwa ukukhutshwa ngokukhawuleza kwe-nucleic acid ye-microbial ekutyeni.

Iimeko zoGcino kunye noMhla wokuphelelwa

Gcina kwiqondo lokushisa, elisebenzayo kwiinyanga ezili-12.

Izixhobo kunye nezinto ezisetyenziswayo

Ibhafu yamanzi okanye i-metal bath, i-centrifuge yesantya esiphezulu (esetyenziselwa isampuli yonyango lwangaphambili), i-pipette, kunye neengcebiso.

Ukusetyenziswa

1.IsampuluPre-unyango

Phatha umfuziselo Jonga kwi-GB4789 okanye eminye imigangatho yoshishino.

2.NUkukhutshwa kwe-ucleic Acid

Thatha i-20 ul yesisombululo sokutyebisa kwi-tube ye-lysate, i-vortex imizuzwana ye-30, i-centrifuge ngokufutshane, kwaye ubeke eceleni.

 Amanqaku: Ukukhutshwa kwe-nucleic acid kwi-lysate kufuneka kugqitywe ngaphakathi kwemizuzu eyi-10 kwaye ayikwazi ukugcinwa ixesha elide.

Ninqaku

1. Kucetyiswa ukuba unxibe iimpahla zokusebenza ezicocekileyo kunye neeglavu ngexesha lovavanyo.Iingcebiso ezisetyenzisiweyo kufuneka zicolwe kwangethuba, kwaye yonke inkunkuma eyenziwe kuvavanyo kufuneka ilahlwe kwangethuba.

2. Nceda ulandele ngokuthe ngqo amanyathelo okusebenza.

3. Nceda usebenzise ikhithi ungadlulanga umhla wokuqinisekisa.


  • Ngaphambili:
  • Okulandelayo:

  • Izikhokelo zohlalutyo lweengxaki

    The following is an analysis of the problems that might be encountered in the extraction of viral RNA. We wish it would be helpful to your experiment. In addition, for other experimental or technical problems other than operating instructions and problem analysis, we have dedicated technical support to help you. Contact us if you need at : 028-83361257or E-mail:Tech@foregene.com。

     

    Akukho RNA inokukhutshwa okanye isivuno se-nucleic acid siphantsi

    Ngokuqhelekileyo zininzi izinto ezichaphazela ukusebenza kakuhle kokubuyisela, ezinje: umxholo we-RNA, indlela yokusebenza, umthamo we-elution, njl.

    Uhlalutyo lwezizathu eziqhelekileyo:

    1.I-ice bath okanye iqondo lokushisa eliphantsi (4 ° C) i-centrifugation ngexesha lokusebenza.

    Ingcebiso: Ubushushu begumbi (15-25 ° C) ukusebenza, ungaze uhlambe umkhenkce kunye nobushushu obuphantsi be-centrifuge.

    2. Ukugcinwa kwesampuli engafanelekanga okanye ukugcinwa kwesampuli ixesha elide.

    Ingcebiso: Gcina iisampulu kwi-80 ° C okanye umkhenkce kwinitrogen engamanzi, kwaye ugweme ukusetyenziswa okuphindaphindiweyo komkhenkce;zama ukusebenzisa iisampulu ezisanda kuqokelelwa ukutsalwa kwe-RNA.

    3.Isampula enganelanga i-lysis

    Isincomo: Nceda uqinisekise ukuba isampuli kunye nesisombululo esisebenzayo (i-Linear Acrylamide) ixutywe ngokucokisekileyo kwaye ifakwe kwi-10 min kwindawo yokushisa (15-25 ° C)

    4.I-eluent yongezwa ngokungalunganga

    Ingcebiso: Qinisekisa ukuba i-ddH2O ye-RNase-Free yongezwa kumbindi wenwebu yekholamu yokucoca.

    5.Umthamo ongafanelekanga we-ethanol ye-anhydrous kwi-Buffer viRW2

    Ingcebiso: Nceda ulandele imiyalelo, yongeza umthamo ochanekileyo we-ethanol ye-anhydrous kwi-Buffer viRW2 kwaye uyixube kakuhle ngaphambi kokusebenzisa ikhithi.

    6.Ukusetyenziswa kwesampulu engafanelekanga.

    Iingcebiso: 200µl yesampulu nge-500μl ye-Buffer viRL.Umthamo wesampulu ogqithisileyo uya kukhokelela ekunciphiseni izinga lokutsalwa kwe-RNA.

    7.Umthamo we-elution ongafanelekanga okanye ukukhutshwa okungaphelelanga.

    Isiphakamiso: Umthamo ocacileyo wekholamu yokucoca yi-30-50μl;ukuba isiphumo asanelisi, kuyacetyiswa ukuba udibanise i-RNase-Free ddH eshushu ngaphambili.2O kunye nokwandisa ixesha lokubeka kwindawo yokushisa, njenge-5-10min

    8.Ikholamu yokucoca inentsalela ye-ethanol emva kokuhlanjululwa kwi-Buffer viRW2.

    Isiphakamiso: Ukuba i-ethanol isala emva kokuhlanjululwa kwi-Buffer viRW2 kunye ne-centrifugation ye-tube engenanto ye-2min, ikholamu yokucoca inokushiywa kwindawo yokushisa ye-5min emva kwe-tube centrifugation engenanto ukususa ngokupheleleyo i-ethanol eseleyo.

     

    Ukonakaliswa kweemolekyuli ze-RNA ezihlambulukileyo

    Umgangatho we-RNA ecocekileyo inxulumene nezinto ezifana nokugcinwa kwesampulu, ukungcoliseka kwe-RNase, kunye nokusebenza.

    Uhlalutyo lwezizathu eziqhelekileyo:

    1.Iisampulu eziqokelelweyo azigcinwanga ngexesha.

    Ingcebiso: Ukuba isampulu ayisetyenziswanga ngexesha emva kokuqokelela, nceda uyigcine ku -80 ℃ okanye initrogen engamanzi ngoko nangoko.Xa kutsalwa iimolekyuli ze-RNA, zama ukusebenzisa iisampulu ezisanda kuqokelelwa xa kunokwenzeka.

    2.Iisampulu eziqokelelweyo zazikhenkceza kwaye zinyibilike ngokuphindaphindiweyo.

    Isiphakamiso: Gwema ukukhenkceza ngokuphindaphindiweyo kunye nokunyibilika (kungekho ngaphezu kweyodwa) ngexesha lokuqokelela isampuli kunye nokugcinwa, ngaphandle koko isivuno se-nucleic acid siya kuncipha.

    3.I-RNase yaziswa kwigumbi lokusebenza okanye akukho ziglavu ezilahlwayo, iimaski, njl.njl.

    Ingcebiso: Ukutsalwa kovavanyo lweemolekyuli ze-RNA kwenziwa ngcono kwigumbi lokusebenza elahlukileyo le-RNA, kwaye itafile yovavanyo iyacocwa phambi kovavanyo.Nxiba iiglavu ezilahlwayo kunye nemaski ngexesha lovavanyo ukunqanda ukuthotywa kwe-RNA okubangelwa kukwaziswa kwe-RNase.

    I-4.I-reagent ingcolisekile yi-RNase ngexesha lokusetyenziswa.

    Ingcebiso: Faka enye iViral RNA Isolation Kit kwimifuniselo ehambelanayo.

    5.Ungcoliseko lwe-RNase yeetyhubhu ze-centrifuge, iingcebiso ze-pipette, njl. Ingcebiso: Qinisekisa ukuba iityhubhu ze-centrifuge, iingcebiso ze-pipette, kunye neepayipi zonke azina-RNase.

     

    Iimolekyuli ze-RNA ezisulungekileyo zichaphazele iimvavanyo ezisezantsi

    Iimolekyuli ze-RNA ezihlanjululwe yikholomu yokucoca ziya kuchaphazela iimvavanyo ezisezantsi ukuba kukho ii-ion zetyuwa ezininzi okanye iiprotheni, ezinje: ukuguqulelwa umva, i-Northern Blot, njl.

    1.Kukho iiyoni zetyuwa ezishiyekileyo kwiimolekyuli ze-RNA eluted.

    Isincomo: Qinisekisa ukuba umthamo ochanekileyo we-ethanol ye-anhydrous yongezwe kwi-Buffer viRW2, kwaye uhlambe ikholamu yokucoca kabini ngokwesantya esichanekileyo se-centrifugation kwimiyalelo yokusebenza; Ukuba kusekho i-ion yetyuwa eseleyo, unokongeza i-Buffer viRW2 kwikholamu yokucoca, kwaye uyishiye kwindawo yokushisa ye-5min.Emva koko yenza i-centrifugation ukususa i-ion yetyuwa ngowona mgangatho mkhulu

    2.Kukho i-ethanol eshiyekileyo kwiimolekyuli ze-RNA

    Isiphakamiso: xa uqinisekisa ukuba iikholomu zokucoca zihlanjululwe yi-Buffer viRW2, yenza i-centrifugation ye-tube engenanto ngokwesantya se-centrifugal kwimiyalelo yokusebenza.Ukuba kusekho i-ethanol eseleyo, inokushiywa imizuzu emi-5 kwiqondo lobushushu begumbi emva kokuba i-centrifugation yetyhubhu engenanto ukususa i-ethanol eseleyo ngowona mlinganiselo mkhulu.

    Izikhokelo zoMyalelo:

    I-Viral RNA Isolation Kit Manual Manual

     

    Bhala umyalezo wakho apha kwaye uwuthumele kuthi