[求救] PCR p不出來
小弟 最近在P一個基因的promoter (GC%=42% 長度=1kb)
所以先從genomic DNA開始做起
然後就是設計primer
我有設計和paper一樣的如下
5' Tm GC%
CCG A/CCGGT GAGCTC AAA TCA GTC AAA CCT AAG AA 65.5 49
------- --------------------------
enzyme cut complement to genomic DNA
3'
GA A/GATCT CTC GAG GGCC ATG GCG CCG GCT CGT GCT T 73.3 65
------- --------------------------
enzyme cut complement to genomic DNA
讓我覺得很奇怪的是 paper為何會在5'端設計多出 GAG CTC 這段序列???
而且還讓 5'和3'primer這端互補(3' CTC GAG)
把它拿去P之後
94(5min) {94(30s)-annealing tm(30s)-72(1min)}30個cycle --72(10min)--4oC
嘗試過annealing 的溫度
56.3 57.4 59.0 60.7 63.2 65 66.6 67.8 68.9 69.3
結果是都沒有P出來 而且在3kb有很強的band(冏)
所以我是不是應該把GAGCTC這段序列拿掉???
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