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作者 FENOR 在 PTT [ Biotech ] 看板的留言(推文), 共94則
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1F推:marker會很糊的話你transfer在設置的時候應該就有問題12/19 09:22
2F→:和protein大小無關12/19 09:22
3F→:270kDa的話要不要試試semidry?12/19 09:23
9F推:讓細胞表現GFP都會產生ER stress,如果放進人體表現10/10 12:03
10F→:後果難以想像,一則細胞會分解GFP,二則當GFP強到可以觀察10/10 12:04
11F→:時人應該也差不多要掛了0RZ10/10 12:04
12F→:用帶著GFP tag的抗體進去的話就會面臨無法觀察的問題10/10 12:05
13F→:至少現在辦不到10/10 12:05
45F推:B才是對的。 UV根本照不透玻璃,所以A的手法做一堆白工08/24 10:34
46F→:A的做法真的有必要的也只有第一步的將去離子水滅菌08/24 10:35
3F推:一樓應該是想要講:如果有認識的有可以告訴原PO去要08/18 12:07
3F推:重抽吧08/16 12:03
1F推:理論上會比55KD略大。至於做IP的實驗,可以用的tag很多08/11 23:13
2F→:有His FLAG HA 等等08/11 23:14
1F推:我會用8字形遙法07/09 16:55
2F推:EDTA是拿來抓Mg2+ Ca2+等二價金屬離子06/19 11:08
3F→:PCR時怎麼可能會加這一項??06/19 11:09
3F推:要用這方法要點運氣06/17 00:14
4F→:也要兩者之間剛好有可以切的06/17 00:14
3F推:XD 還要接電線啊!06/12 18:54
6F→:而且要做clone,還是少不了電泳啊06/12 19:20