作者查詢 / ppppai
作者 ppppai 在 PTT [ Biotech ] 看板的留言(推文), 共34則
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2F推:有可能都在膜上,我之前會再用buffer沖membrane就會有了!05/19 13:35
1F→:不同病毒應該不同吧 建議做plaque assay test05/14 16:50
6F→:推樓上T大方法 注意無菌操作即可05/14 16:49
1F推:Trypan blue通過細胞膜染死細胞 活細胞不就沒染到的就是嗎?05/14 16:47
2F→:真菌? 是yeast嗎?05/14 16:47
3F→:另外也可染膜上的marker 像receptor之類的05/14 16:48
7F推:若想看PCD通常會用Flow cytometry看,但不知絲狀真菌可否看05/15 16:14
5F推:會是phenol-chloroform弄不乾淨嗎?05/14 17:03
11F→:我是用human-like robot 洗片XDD 就是手工萬歲啦05/14 16:37
12F→:樓上t大 我確定不會有這樣的事05/14 16:38
13F→:顯定影劑都新配沒多久05/14 16:39
14F→:若是gel的問題的話...同樣的buffer, 我用國產東生公司的會05/14 16:40
15F→:很sharp但若用Hoefer系就會糊糊...而且還會很多雜band...05/14 16:41
16F→:但hoefer超多人用就沒問題,但在我這用就會! 超怪!05/14 16:42
17F→:然後小抱怨一下,因為我家老闆的結論是那就不要用Hoefer跑05/14 16:42
4F→:用有AmpR的菌test看看 拿新配的LB Amp當control 算菌落數05/14 16:52
1F推:我之前不加甘油 用液氮快速冷凍再放-7005/13 20:13
6F→:有查NEB看你的限制酶有無特殊note?05/14 17:05
7F→:之前我有切不動的情形是因為plasmidDNA在細菌中太舊才抽出05/14 17:05
8F→:導致可能被甲基化,所以切不動,再把DNA重新transform重抽05/14 17:06
9F→:就不會了05/14 17:06
10F→: 久 (錯字)05/14 17:07
11F→:注: 太久= transform菌養2ml離心後直接凍-20超過一個月後抽05/14 17:09
10F推:是用site-directed kit嗎?05/13 20:15