<td id="wa4yw"><option id="wa4yw"></option></td>
  • <td id="wa4yw"><kbd id="wa4yw"></kbd></td><noscript id="wa4yw"><source id="wa4yw"></source></noscript>
    <bdo id="wa4yw"><kbd id="wa4yw"></kbd></bdo><input id="wa4yw"></input>
    <table id="wa4yw"><kbd id="wa4yw"></kbd></table>
  • <td id="wa4yw"><option id="wa4yw"></option></td>
    <option id="wa4yw"></option>
  • <table id="wa4yw"></table>
  • 發布時間:2019-05-20 19:06 原文鏈接: YeastGeneknockoutusingOligo/PCR

    Universal primers for gene knock-out using dominant drug markers: Kan, Clonat, and Hygromisin-B. 

    Forward primer: 5’ TCAGGGGCATGATGTGACT 3’
    Reverse primer: 5’ AGCTCGTTTTCGACACTGGAT 3’


    Plasmids for Selectable Markers
    Plasmid for amplifying Kan:pKan-GenMX4.seq (GCK), product size: ~1.4kb.
    Plasmid for amplifying Clonat:pAG25-ClonatMX4.seq (GCK), product size: ~1.2kb.
    Plasmid for amplifying HB:pAG32-hphMX4.seq (GCK), product size: ~1.5kb.

    PCR condition:
    1. 95°C for 5 minutes
    2. 95°C for 30 seconds
    3. 57°C for 1 minute
    4. 72°C for 3 minutes
    5. Repeat steps 2 to 4 for 30 cycles
    6. 72°C for 5 minutes
    7. 4°C Forever


    Primers for colony 
    PCR to confirm gene knockout using Kan, Clonat, and HB.
    For Kan:
    Forward: KanMX4F1: 5’ ATTCTCACCGGATTCAGTCGT 3’ 
    Reserve: KanMXR1: 5’ AATCCGGTGAGAATGGCAAA 3’ 
    For Clonat:
    Reverse: NatMX4R1: 5’ ATTCGTCGTCCGATTCGT 3’ 
    For H-B:
    Forward: hphMX4F1: 5’ TACACAAATCGCCCGCAGAA 3’
    Reverse: hphMX4R1: 5’ TCGGTTTCAGGCAGGTCTT 3’ 


    You need to design a 
    PCR primer for your gene of interest to make it work. 

    <td id="wa4yw"><option id="wa4yw"></option></td>
  • <td id="wa4yw"><kbd id="wa4yw"></kbd></td><noscript id="wa4yw"><source id="wa4yw"></source></noscript>
    <bdo id="wa4yw"><kbd id="wa4yw"></kbd></bdo><input id="wa4yw"></input>
    <table id="wa4yw"><kbd id="wa4yw"></kbd></table>
  • <td id="wa4yw"><option id="wa4yw"></option></td>
    <option id="wa4yw"></option>
  • <table id="wa4yw"></table>
  • XVideos