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Foreasy HS Taq DNA Polymerase

Kit Description:

Yakanyanya kujeka: Iyo enzyme ine yakanyanya kupisa-kutanga basa.

Kukurumidza Kuwedzera: 10 sec/kb.

Yakakwira template kuchinjika: inogona kushandiswa kunyatso kusimudzira YakakwiriraGCvalueuyezvakasiyana-siyana zvakaoma-ku-kurisa DNA template.

Kuvimbika kwakasimba: Kuvimbika ndiko 6 nguvaof zvakajairika Taq Enzyme.

foregene simba


Product Detail

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FAQ

Tsanangudzo

Foreasy HS Taq DNA Polymerase inyowani itsva yeTaq inoratidzwa muEscherichia coli engineering bhakitiriya nejene recombination tekinoroji.Mushure mokunge enzyme inobatwa nemaitiro anokosha, iyo's chiitiko chinodzivirirwa kusati kwaitwa thermal activation, nekudaro ichivharira iyo isiri-chaiyo amplification inokonzerwa neiyo isiri-chaiyo annealing yemaprimers kana primer dimers pasi pemamiriro ekushisa akaderera.Ichi chigadzirwa chakakodzera zvakanyanya chaiyo PCR Reaction, M ultiple x PCR , yakakwira GC zvirimo (> 60%) ,pamwechimiro chechipirikana zvimweyakasimba background genomicsamplification uye yakakura-chiyero genomicsamplification kuona.Iyo enzyme ine 5' → 3' DNA polymerase chiitiko uye 5' → 3' exonuclease chiitiko, asi hapana 3' → 5' exonuclease chiitiko.

Kit zvikamu

Chikamu IM-01021 IM-01022 IM-01023
Foreasy HS Taq DNA Polymerase (5 U/μL)  5000 U (1 mL)  50 KU (10 mL)  500 KU (100 mL)
2 × Taq Reaction Buffer  25mL ×5  250 mL ×5  500 mL × 25

Zvimiro&zvakanakira

- Yakanyanya kujeka: Iyo enzyme ine yakanyanya kupisa-yekutanga chiitiko.

-Kukurumidza Kusimudzira: 10 sec/kb.

-Yakakwira template kuchinjika: inogona kushandiswa kunyatso kusimudzira YakakwiriraGCvalueuyezvakasiyana-siyana zvakaoma-ku-kurisa DNA template.

- Kuvimbika kwakasimba: Kutendeseka ndiko katanhatuof zvakajairika Taq Enzyme.

Kit application

- Yakasiyana PCR/qPCR System uye yakananga PCR system

- PCR Yakawedzera DNA Chimedu

- DNA chiratidzo

- DNA Sequencing

- PCR pamwe nemuswe

Chiitiko Tsanangudzo

1U: Huwandu hwe enzyme inodiwa kuisa gumi nmol yeDNAmuasidhi-isina kunyungudika uchishandisa yakagadziriswa salmon urume DNA setemplate / primer, 74 °C, 30 maminetsi.

Reaction Condition

Tembiricha Reaction Time Cycle time
37°C 5 min 1
94°C 5 min 1
94°C 10 Secs  40
60°C 10 Secs

Cherechedza:Kune 10 µL uye 20 µL masisitimu, wedzera huwandu hwakaenzana hwemafuta emaminerari kana thermal cycler isina chivharo chekupisa.

Mamiriro ekuita PCR anosiyana zvichienderana nemamiriro ekugadzirisa matemplate, maprimers, nezvimwe zvakadaro.Mukushanda chaiko, zvinodikanwa kugadzira iwo akanyatsoita maitiro, anosanganisira annealing tembiricha, nguva yekuwedzera, nezvimwe, zvinoenderana nemamiriro chaiwo akadai semhando yetemplate, saizi yechinhu chakanangwa chidimbu, kutevedzana kwehwaro hwechimedu chakasimudzirwa, uye iyo GC yemukati uye kureba kweiyo primer.

Storage

-20 ± 5 °C kwemakore maviri kana -80 °C kwekuchengetedza kwenguva refu.


  • Zvakapfuura:
  • Zvinotevera:

  • Hapana masaini ekuwedzera

    1.Taq DNA Polymerase mukiti inorasikirwa nebasa rayo nekuda kwekuchengetedza kusina kunaka kana kupera kwekiti.
    Kurudziro: Simbisa mamiriro ekuchengetedza ekiti;wedzerazve huwandu hwakakodzera hweTaq DNA Polymerase kuPCR system kana kutenga itsva Real Time PCR Kit yezviedzo zvinoenderana.

    2.Kune akawanda inhibitors yeTaq DNA Polymerase muDNA template.
    Zvaungaita: Natsazve template kana kuderedza huwandu hwetemplate yakashandiswa.

    3.Mg2 + concentration haina kukodzera.
    Kurudziro: Iyo Mg2 + yekumisikidza ye2 × Real PCR Mix yatinopa ndeye 3.5mM.Nekudaro, kune mamwe akakosha ekutanga uye matemplate, iyo Mg2 + yekumisikidza inogona kunge yakakwira.Naizvozvo, unogona kuwedzera zvakananga MgCl2 kukwidziridza iyo Mg2+ concentration.Zvinokurudzirwa kuwedzera iyo Mg2+ 0.5mM nguva yega yega kuitira optimization.

    4.Iyo PCR amplification mamiriro haana kukodzera, uye kutevedzana kweprimer kana kuisa pfungwa hakuna kunaka.
    Mazano: simbisa kururamisa kwekutevedzana kweprimer uye primer haina kuderedzwa;kana chiratidzo chekusimudzira chisina kunaka, edza kudzikisira tembiricha yekumisa uye gadzirisa iyo primer concentration nenzira kwayo.

    5.Kuwanda kwe template kuduku kana kuwanda.
    Kurudziro: Ita template linearization gradient dilution, uye sarudza iyo template yekumisikidza ine yakanakisa PCR mhedzisiro yeChaiyo Nguva PCR kuyedza.

    NTC ine yakawandisa fluorescence kukosha

    1.Reagent kusvibiswa kunokonzerwa panguva yekushanda.
    Kurudziro: Tsiva nema reagents eChaiyo Nguva PCR kuyedza.

    2.Kusvibiswa kwakaitika panguva yekugadzirira kwePCR reaction system.
    Kurudziro: Tora matanho ekudzivirira anodiwa panguva yekushanda, senge: kupfeka magurovhosi e latex, kushandisa piipi tipi ine sefa, nezvimwe.

    3.The primers yakasvibiswa, uye kuderedzwa kwezvinyorwa kuchaita kuti kusava kwakananga amplification.
    Kurudziro: Shandisa SDS-PAGE electrophoresis kuona kana maprimers akashatiswa, woatsiva nemaprimer matsva eChaiyo Nguva PCR kuyedza.

    Primer dimer kana kuti non-specific amplification

    1.Mg2 + concentration haina kukodzera.
    Kurudziro: Iyo Mg2 + yepakati ye2 × Real PCR EasyTM Mix yatinopa ndeye 3.5 mM.Nekudaro, kune mamwe akakosha ekutanga uye matemplate, iyo Mg2 + yekumisikidza inogona kunge yakakwira.Naizvozvo, unogona kuwedzera zvakananga MgCl2 kukwidziridza iyo Mg2+ concentration.Zvinokurudzirwa kuwedzera iyo Mg2+ 0.5mM nguva yega yega kuitira optimization.

    2.The PCR annealing tembiricha yakaderera.
    Zano: Wedzera tembiricha yePCR annealing ne1 ℃ kana 2 ℃ nguva yega yega.

    3.Chigadzirwa chePCR chakareba.
    Kurudziro: Hurefu hweiyo Real Time PCR chigadzirwa hunofanirwa kunge huri pakati pe100-150bp, kwete kupfuura 500bp.

    4.The primers yakasvibiswa, uye kusvibiswa kwezvinyorwa zvinotungamirira pakuonekwa kwekuwedzerwa kwakananga.
    Kurudziro: Shandisa SDS-PAGE electrophoresis kuona kana maprimers akashatiswa, woatsiva nemaprimer matsva eChaiyo Nguva PCR kuyedza.

    5.Iyo PCR system haina kunaka, kana hurongwa hwakanyanya kuduku.
    Zano: Iyo PCR reaction system idiki zvakanyanya inokonzeresa kuti yekuona iderere.Zvakanakisa kushandisa reaction system inokurudzirwa neakawanda PCR chiridzwa kumhanyisa zvakare Yechokwadi Nguva PCR kuyedza.

    Kusagona kudzokororwa kwehuwandu hunokosha

    1.Chiridzwa chiri kutadza kushanda.
    Zano: Panogona kunge paine kukanganisa pakati pegomba rega rega rePCR yechiridzwa, zvichikonzera kusaberekana zvakanaka panguva yekutarisira tembiricha kana kuona.Ndokumbira utarise maererano nemirairo yechiridzwa chinoenderana.

    2.Kuchena kwemuenzaniso hakuna kunaka.
    Kurudziro: Samples dzisina kuchena dzinotungamira mukutadza kuberekana kwekuyedza, izvo zvinosanganisira kuchena kwetemplate uye yekutanga.Zvakanakisa kuchenesa template, uye iyo yekutanga inonatswa zvakanyanya neSDS-PAGE.

    3.Iyo PCR system yekugadzirira uye nguva yekuchengetedza yakanyanyisa.
    Kurudziro: Shandisa iyo Real Time PCR system yePCR kuyedza nekukurumidza mushure mekugadzirira, uye usaisiye parutivi kwenguva yakareba.

    4.Iyo PCR amplification mamiriro haana kukodzera, uye kutevedzana kweprimer kana kuisa pfungwa hakuna kunaka.
    Mazano: simbisa kururamisa kwekutevedzana kweprimer uye primer haina kuderedzwa;kana chiratidzo chekusimudzira chisina kunaka, edza kudzikisira tembiricha yekumisa uye gadzirisa iyo primer concentration nenzira kwayo.

    5.Iyo PCR system haina kunaka, kana hurongwa hwakanyanya kuduku.
    Zano: Iyo PCR reaction system idiki zvakanyanya inokonzeresa kuti yekuona iderere.Zvakanakisa kushandisa reaction system inokurudzirwa neakawanda PCR chiridzwa kumhanyisa zvakare Yechokwadi Nguva PCR kuyedza.

    Nyora meseji yako pano ugotitumira