Sihlala sisenza ukuba singabasebenzi ababambekayo siqinisekisa ukuba siya kukunika elona xabiso libalaseleyo kunye nelona xabiso lilungileyo lokuthengisa le-4X DNA Rna Inyathelo elinye le-Rt-Qpcr Multiplex Master Mix Kit, siza kuqhuba sizama ukunyusa inkampani yethu kwaye sibonelele ngezona mveliso zisemgangathweni ezinoluhlu lwamaxabiso anobundlongondlongo.Nawuphi na umbuzo okanye izimvo zixatyiswa kakhulu.Khumbula ukusibamba ngokukhululekileyo.
Sidla ngokwenza ukuba singabasebenzi ababambekayo siqinisekisa ukuba siya kukunika elona ncedo lubalaseleyo kunye nelona xabiso lilungileyo lokuthengisaI-China Taq DNA Polymerase kunye ne-Qpcr, Ngendibano yocweyo ehambele phambili, iqela loyilo lobuchwephesha kunye nenkqubo engqongqo yolawulo lomgangatho, esekwe kumbindi ukuya kwisiphelo esiphezulu esiphawulwe njengendawo yokuthengisa, iimveliso zethu zithengiswa ngokukhawuleza kwiimarike zaseYurophu nezaseMelika ngeempawu zethu ezinje ngasezantsi kweDeniya, Qingsiya kunye neYisilanya.

Iinkcazelo Kit

I-2X yokwenyani PCR Easy^TMI-Mix-Taqman enikezelwa yi-Real Time PCR Easy^TM-Ikhithi ye-Taqman yinkqubo entsha ye-premix esebenzisa i-fluorescent probes ye-Real Time PCR reactions amplification, enokuphucula kakhulu imveliso ethile kunye novakalelo lokuphendula.I-ROX inikezelwa njengedayi yolawulo lwangaphakathi.

2X Real PCR Easy^TMI-Mix-Taqman iqulethe i-Foregene eshushu-isiqalo esisodwa se-Taq DNA Polymerase.Xa kuthelekiswa nee-enzymes ze-Taq eziqhelekileyo, ineengenelo zokusebenza kwe-amplification ephezulu, isakhono esithile esinamandla sokukhulisa kunye nesantya esisezantsi sokungahambelani.Inokunciphisa ukukhuliswa okungangqaliyo kunye nokuphucula ukuchaneka kwe-PCR.

Iinkcukacha

Iimpawu&izinto eziluncedo

■ Ilula—I-2X PCR Mix ukunciphisa impazamo yovavanyo kunye nexesha lokusebenza

■ I-Specific-optimized buffer kunye ne-hot-start Taq enzyme inokuthintela ukukhulisa okungangqalanga kunye nokwakheka kwe-primer dimer.

■ Uvakalelo oluphezulu-lukwazi ukubona iikopi ezisezantsi zetemplate

■ Ukuguquguquka okuhle—okuhambelana nezixhobo ezininzi zePCR zexesha lokwenyani

Isicelo seKit

Uhlalutyo lwe-qPCR

Ukuhamba komsebenzi

Umzobo

Ukugcinwa kunye nobomi beshelufu

Le khithi kufuneka igcinwe kude nokukhanya kwaye kufuneka igcinwe ku -20 ℃.Ukuba isetyenziswe rhoqo, inokugcinwa kwi-4 ℃ ixesha elifutshane (iintsuku ezili-10).

Sihlala sisenza ukuba singabasebenzi ababambekayo siqinisekisa ukuba siya kukunika elona xabiso libalaseleyo kunye nelona xabiso lilungileyo lokuthengisa le-OEM/ODM Supplier High Sensitivity One-Inyathelo le-Rt-Qpcr Multiplex Master Mix Kit, Siza kuqhuba sizama ukunyusa inkampani yethu kwaye sinikezele ngezona mveliso zisemgangathweni ezinoluhlu lwamaxabiso anobundlongondlongo.Nawuphi na umbuzo okanye izimvo zixatyiswa kakhulu.Khumbula ukusibamba ngokukhululekileyo.
OEM / ODM SupplierI-China Taq DNA Polymerase kunye ne-Qpcr, Ngendibano yocweyo ehambele phambili, iqela loyilo lobuchwephesha kunye nenkqubo engqongqo yolawulo lomgangatho, esekwe kumbindi ukuya kwisiphelo esiphezulu esiphawulwe njengendawo yokuthengisa, iimveliso zethu zithengiswa ngokukhawuleza kwiimarike zaseYurophu nezaseMelika ngeempawu zethu ezinje ngasezantsi kweDeniya, Qingsiya kunye neYisilanya.

Akukho miqondiso yokukhulisa

I-1.I-Taq DNA Polymerase kwikiti ilahlekelwa ngumsebenzi wayo ngenxa yokugcinwa okungafanelekanga okanye ukuphelelwa yisikhathi kwekiti.
Ingcebiso: Qinisekisa imiqathango yokugcina ikhithi;yongeza kwakhona imali efanelekileyo ye-Taq DNA Polymerase kwinkqubo ye-PCR okanye uthenge i-Real Time PCR Kit kwimifuniselo ehambelanayo.

2.Zininzi ii-inhibitors ze-Taq DNA Polymerase kwi-template ye-DNA.
Ingcebiso: Hlaziya itemplate okanye unciphise inani letemplate esetyenzisiweyo.

3.I-concentration ye-Mg2 + ayifanelekanga.
Isincomo: I-Mg2 + yoxinaniso lwe-2× Real PCR Mix esibonelela ngayo yi-3.5mM.Nangona kunjalo, kwezinye iiprimers ezikhethekileyo kunye neetemplates, ugxininiso lweMg2 + lunokuba phezulu.Ke ngoko, unokongeza ngokuthe ngqo i-MgCl2 ukongeza i-Mg2+ yoxinaniso.Kuyacetyiswa ukuba kwandiswe i-Mg2+ 0.5mM ixesha ngalinye ukwenzela ukuba kuphuculwe.

4.Iimeko zokukhulisa i-PCR azifanelekanga, kwaye ukulandelelana kwe-primer okanye ukugxininiswa akufanelekile.
Isiphakamiso: qinisekisa ukuchaneka kokulandelelana kwe-primer kwaye i-primer ayizange ithotywe;ukuba isignali yokukhulisa i-amplification ayilungile, zama ukuthoba iqondo lokushisa le-annealing kwaye ulungelelanise i-primer concentration ngokufanelekileyo.

5.Isixa setemplate sincinci okanye sininzi kakhulu.
Isincomo: Yenza ithempleyithi yohlengahlengiso lodidi, kwaye ukhethe itemplate yoxinaniso ngeyona mpembelelo ilungileyo yePCR kulingo lwexesha lokwenyani lwePCR.

I-NTC inexabiso eliphezulu kakhulu le-fluorescence

Ungcoliseko lwe-1.Reagent olubangelwa ngexesha lokusebenza.
Isincomo: Faka indawo ngezinto ezintsha zokuvavanya ixesha lokwenyani lePCR.

2.Ungcoliseko lwenzekile ngexesha lokulungiselela inkqubo yokusabela kwe-PCR.
Isincomo: Thatha imilinganiselo yokukhusela eyimfuneko ngexesha lokusebenza, njengale: ukugqoka iiglavu ze-latex, usebenzisa i-pipetti tip kunye nesihlungi, njl.

3.Ii-primers zihlanjululwe, kwaye ukuthotywa kwee-primers kuya kubangela ukukhulisa okungangqalanga.
Ingcebiso: Sebenzisa i-SDS-PAGE i-electrophoresis ukubona ukuba iiprimers zithotyiwe, kwaye ubeke endaweni yazo ngeeprimer ezintsha zeLixesha loNyaniso lwemifuniselo yePCR.

Primer dimer okanye non-specific amplification

I-1.I-concentration ye-Mg2 + ayifanelekanga.
Isincomo: I-Mg2 + yoxinaniso lwe-2 × Real PCR Easy TM Mix esibonelela ngayo yi-3.5 mM.Nangona kunjalo, kwezinye iiprimers ezikhethekileyo kunye neetemplates, ugxininiso lweMg2 + lunokuba phezulu.Ke ngoko, unokongeza ngokuthe ngqo i-MgCl2 ukongeza i-Mg2+ yoxinaniso.Kuyacetyiswa ukuba kwandiswe i-Mg2+ 0.5mM ixesha ngalinye ukwenzela ukuba kuphuculwe.

2.Iqondo lobushushu le-PCR liphantsi kakhulu.
Ingcebiso: Yongeza iqondo lobushushu le-PCR nge-1℃ okanye nge-2℃ ngexesha ngalinye.

3.Imveliso yePCR inde kakhulu.
Isincomo: Ubude be-Real Time PCR imveliso kufuneka ibe phakathi kwe-100-150bp, ingabi ngaphezu kwe-500bp.

4.Ii-primers zihlanjululwe, kwaye ukuchithwa kwee-primers kuya kukhokelela ekubonakaleni kwe-amplification ethile.
Ingcebiso: Sebenzisa i-SDS-PAGE i-electrophoresis ukubona ukuba iiprimers zithotyiwe, kwaye ubeke endaweni yazo ngeeprimer ezintsha zeLixesha loNyaniso lwemifuniselo yePCR.

I-5.Inkqubo ye-PCR ayifanelekanga, okanye inkqubo incinci kakhulu.
Ingcebiso: Inkqubo yokusabela ye-PCR incinci kakhulu iya kubangela ukuchaneka kobhaqo ukuba kwehle.Kungcono ukusebenzisa inkqubo yokusabela ekhuthazwa sisixhobo sobungakanani bePCR ukuphinda usebenzise umfuniselo weXesha lokwenyani wePCR.

Ukuphindaphinda okulambathayo kwamaxabiso obungakanani

1.Isixhobo asisebenzi kakuhle.
Isiphakamiso: Kunokubakho iimpazamo phakathi komngxuma ngamnye we-PCR wesixhobo, okubangela ukuveliswa kakubi ngexesha lokulawula ubushushu okanye ukufumanisa.Nceda ujonge ngokwemiyalelo yesixhobo esihambelanayo.

2.Ubunyulu besampula ayilungile.
Isincomo: Iisampulu ezingcolileyo ziya kukhokelela ekuveliseni okungahambi kakuhle kovavanyo, okubandakanya ukucoceka kwetemplate kunye neeprimers.Kungcono ukuhlambulula itemplate, kwaye i-primers ihlanjululwe kakuhle yi-SDS-PAGE.

I-3.I-PCR yokulungiselela inkqubo kunye nexesha lokugcinwa lide kakhulu.
Ingcebiso: Sebenzisa inkqubo ye-PCR yeXesha lokwenyani yovavanyo lwe-PCR ngoko nangoko emva kolungiselelo, kwaye ungayishiyi ecaleni ixesha elide.

4.Iimeko zokukhulisa i-PCR azifanelekanga, kwaye ukulandelelana kwe-primer okanye ukugxininiswa akufanelekile.
Isiphakamiso: qinisekisa ukuchaneka kokulandelelana kwe-primer kwaye i-primer ayizange ithotywe;ukuba isignali yokukhulisa i-amplification ayilungile, zama ukuthoba iqondo lokushisa le-annealing kwaye ulungelelanise i-primer concentration ngokufanelekileyo.

I-5.Inkqubo ye-PCR ayifanelekanga, okanye inkqubo incinci kakhulu.
Ingcebiso: Inkqubo yokusabela ye-PCR incinci kakhulu iya kubangela ukuchaneka kobhaqo ukuba kwehle.Kungcono ukusebenzisa inkqubo yokusabela ekhuthazwa sisixhobo sobungakanani bePCR ukuphinda usebenzise umfuniselo weXesha lokwenyani wePCR.