作者查詢 / bluecsky
作者 bluecsky 在 PTT [ Biotech ] 看板的留言(推文), 共687則
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3F推:多換幾次buffer比轉速快慢有用多了 個人感覺..07/01 00:39
4F→:除非慢到誇張啦 不然buffer多換還比較好 只是就很浪費XD07/01 00:40
16F推:跑大分子的transfer不是要降低MeOH 提高一些SDS嗎??06/27 13:14
4F推:ligation RT 1hr...你對你的ligase真有信心..06/25 15:38
5F→:一邊blunt end 一邊sticky end應該不會太過難接06/25 15:38
6F→:試試看把ligation時間拉長點看看 可考慮4度冰箱擺隔夜06/25 15:39
7F→:當然competent cell的品質影響也是很大 也可以試試06/25 15:40
27F推:直接整罐配好再分裝去-20凍起來不就好 ? 可以拿一些06/21 19:52
28F→:去4度放者 我們lab都這樣做 APS還沒出過問題06/21 19:53
1F推:因為二抗很便宜 所以多買幾支大多數lab還可應付XD06/20 10:54
2F→:了不起去跟隔壁的lab問問 大多二抗也就幾種06/20 10:54
3F→:anti-rat mouse rabbit goat...大多不出這幾種吧06/20 10:55
5F推:你就想成 基因槍是靠火藥硬把DNA片段送進去細胞中06/12 05:51
17F推:重頭做最穩 不然這東西你也不確定純不純 做到最後發現06/03 08:18
18F→:都錯了才從頭的話 不是更浪費時間嗎?06/03 08:19
3F推:我們lab常用大tank 大約每次都倒掉一些舊的加一些新的06/01 22:13
4F→:不然每幾次就要配個5L的buffer應該會瘋掉06/01 22:14
4F推:supercoil form跑得比linear form低不是很正常嗎XD05/25 19:02
5F→:你的問題是在於為何應該掉一段insert出來卻沒掉嗎?05/25 19:03
6F→:而且plasmid 7.5k直接跑的話應該會比7k還低歐05/25 19:03
7F→:最有可能就是你拿到的map跟你的plasmid不合05/25 19:04
8F→:所以你的plasmid已經有修改過了 可能接過什麼東西05/25 19:04
7F推:其實切久一點在配上CIP處理 就不太怕單切的問題了05/22 08:22