作者查詢 / GanLinBa
作者 GanLinBa 在 PTT [ Biotech ] 看板的留言(推文), 共32則
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2F→: 新的 trizma 我怎麼配都差不多10左右10/03 17:16
3F→: 我看trimza base datasheet pH10.5-2210/03 17:17
5F→: trypsin 如何取single cell 感謝07/24 06:56
2F→: 可試試看05/29 04:04
1F→: 1. 選B 因為Gem-R應該對20nM以下無反應 如果要看08/14 20:00
2F→: survival 相對於paerental 應該會選B08/14 20:01
3F→: 2. 所以在knockdown完後 maintain細胞就只要加puromycin08/14 20:01
4F→: 然後做實驗時 再用gemcitabine去跟Gem-R-shLuc去做08/14 20:02
5F→: virus knockdown我都是用pool 只是maintanin時08/14 20:03
6F→: 我認為是只要puromcyin去maintain這株Gem-R-shX gene08/14 20:04
7F→: 但因為我實驗室學姐說也要加Gemcitabine去maintanin08/14 20:04
8F→: 如果我對你的話有理解錯誤 請指正08/14 20:06
9F→: http://0rz.tw/qHD6Y08/14 21:11
10F→: 學姊建議是Gem+Puro 而我是想應該是Puro就好08/14 21:12
11F→: 所以答案是maintain只要puro?08/14 21:12
7F→: 感謝08/10 15:43
12F→: resistant cell line 是篩出來的08/10 23:37
15F→: maintain會 但如果要做gemcitabine的影響會加08/14 20:08
16F→: 但如果我想看microenviroment對resistant cell line08/14 20:08
17F→: 就不會08/14 20:08
1F→: 已徵到12/03 23:05
3F→: 感謝1f 所以flag 和 我的protein 都會有10/30 10:47
4F→: 但用flag antibody 可能就壓不到我protein位子10/30 10:48
5F→: 也就是IP即使抓得到flag但沒我的protein在上面?10/30 10:49
2F→: 感謝!!08/30 12:24
1F推:你的transwell應該是指24well的insert 用於migration。03/14 02:49
2F→:孔徑0.8。而coculture0.4 一般tumor不易掉落 一般用於6we03/14 02:49
3F推:在microenviroment上。像macrophage有些是直接去接觸tumo03/14 02:53
4F→:r 而有些是macrophage釋放些chemokine等去影響tumor或是03/14 02:54
5F→:反過來。也可以去看para或auto03/14 02:54
2F→:感謝08/29 23:33