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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1F推:我比較想知道你老闆給你多少預算做這個..XD11/28 20:46
4F推:應該說blunt end比較需要CIP處理一下11/19 20:07
5F→:CIP是去掉5'的磷酸..避免兩個blunt end成self-ligation11/19 20:07
6F→:sticky end不是不能用..而是不需要..11/19 20:09
7F→:因為兩個都是stick end的話是無法self-ligation的11/19 20:09
9F推:哈..感謝樓上幫我補正11/20 08:03
1F推:壓片是能夠一次壓好幾張沒錯..不過顏色應該都一樣11/07 09:15
2F→:應該只有黑色而已吧..壓不同抗體應該是說11/07 09:16
3F→:一張底片能夠壓好幾張membrane..11/07 09:17
4F→:AP的顏色比較漂亮啦..壓片的靈敏度比較高吧11/07 09:17
5F→:壓的時間拉長可以讓一些不明顯的也顯示出來11/07 09:18
6F推:喝水都可以死人了XD11/03 15:39
5F推:其實多看別人呈現的data都會有這些吧XD11/03 10:22
1F推:STAT1我還是會念S-T-A-T-ONE耶.11/01 19:29
1F推:感謝..問題已解決..因為我跑的SAMPLE中就有overexpress10/29 19:27
2F→:給老師看的結果是一樣認不到(我同時有跑mutant跟WT)10/29 19:27
3F→:所以是抗體根本不能用..因為這是我第一次用非comercial10/29 19:27
4F→:的anti-body..所以跑出很多bnad心裡很慌亂..10/29 19:28
4F推:氣泡應該是會transfer不完全..糊掉我想應該是過熱10/17 01:44
5F→:BUFFER都先冰等要跑再拿出來..然後把電泳槽埋在冰裡跑10/17 01:45
6F→:或是把電泳槽拿去冰箱跑也可以..在不然10/17 01:45
7F→:就用低電壓跑久一點..我看過有人是放冷房用10V跑隔夜的10/17 01:46
5F推:所以一般軟體算的原來是denature的阿10/07 16:01
6F→:原來如此..我沒考慮到修飾的問題10/07 16:03
2F→:沒有抗體怎麼做western...囧09/16 20:18
3F→:還是R大的意思是說抓his-tag的抗體?..有這種東西嗎?09/16 20:19
5F推:原來如此阿..那去找找有沒有相對應的anti-body..09/16 20:21
7F→:了解..不然這樣盲目的搞下去也不知道何時能了..= =09/16 20:23
8F→:不過我的目標protein是一個transmembrane protein..09/16 20:24
9F→:會比較難以誘導或是純化嗎?09/16 20:24
13F推:跟據QIAGEN的手冊配的..lysis buffer中有10mM的imidazole09/19 00:36