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| == Re-trying with new cDNA sample. == | == Re-trying with new cDNA sample. == | ||
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| - | ##Overview | ||
| - | ^ Step ^ Description ^ Date/Initials ^ Link protocol ^ Link results ^ | ||
| - | | 1 | Total RNA extraction from HEK293T cells | 20191122DEY | | | | ||
| - | | 2 | 1st strand cDNA synthesis | 20191122DEY | | | | ||
| - | | **3** | **Target gene amplification from cDNA sample** | Current | | | | ||
| - | | 4 | BP-reaction | | | | | ||
| - | | 5 | Sanger sequence check | | | | | ||
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| #### Material | #### Material | ||
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| - | Before preparing: Check your primer Tm at NEB website (http://tmcalculator.neb.com/#!/main with Phusion/HF buffer setting) | ||
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| #### Protocol | #### Protocol | ||
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| ^ Frd primer | PI 11 | PI 11 | PI 13 | PI 13 | PI 15 | PI 15 | PI 17 | PI 17 | PI 19 | PI 19 | | ^ Frd primer | PI 11 | PI 11 | PI 13 | PI 13 | PI 15 | PI 15 | PI 17 | PI 17 | PI 19 | PI 19 | | ||
| ^ Rvs Primer | PI 12 | PI 12 | PI 14 | PI 14 | PI 16 | PI 16 | PI 18 | PI 18 | PI 20 | PI 20 | | ^ Rvs Primer | PI 12 | PI 12 | PI 14 | PI 14 | PI 16 | PI 16 | PI 18 | PI 18 | PI 20 | PI 20 | | ||
| - | + | | Tm | 56 | 56 | 58 | 58 | 65 | 65 | 56 | 56 | 57 | 57 | | |
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| *Mix the following reagents in one tube (ideally from top to bottom) | *Mix the following reagents in one tube (ideally from top to bottom) | ||
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| - | --- //[[daney@sfc.keio.ac.jp|Dan Yamamoto-Evans]] 2019/11/25 14:48// | + | --- //[[daney@sfc.keio.ac.jp|Dan Yamamoto-Evans]] 2019/12/10 11:37// |
| **Print at 96%** | **Print at 96%** | ||