作者查詢 / Anvec
作者 Anvec 在 PTT [ Biotech ] 看板的留言(推文), 共104則
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7F→: 這應該可信度不低吧 質譜打出的片段 有對到CYTB_RAT 3個位11/29 13:13
8F→: 置 佔了全部序列的79%11/29 13:13
9F→: 因為用 Trypsin 切 每段的屁股都是K11/29 13:14
11F→: 啊 5段序列11/29 13:15
7F→:Urea 溶解後 整杯的體積會增加唷 所以要先溶再補滿體積02/02 08:56
8F→:加熱有助於溶解 但是Urea在30度上下很容易裂解02/02 09:02
9F→:如果你的樣品是蛋白質 就會修飾你的蛋白質樣品02/02 09:03
10F→:http://www.ionsource.com/Card/carbam/carbam1.gif02/02 09:03
17F→:請用 tris-base 配下層膠唷 沒意外的話配好的 pH 應該是對的12/13 22:49
18F→:你把緩衝用的溶液從 pH 6.8 滴定到 pH 8.8 它就沒有緩衝效果12/13 22:49
19F→:那跑到最後 pH 值一定會越來越酸12/13 22:50
17F→:實驗做不出來 有很多很多因素 有時候是不被發覺的地方08/28 07:38
18F→:比如電源供應器的穩定性 建議你直接去你同學的實驗室做一次08/28 07:38
19F→:排除是操作問題後 再一個一個試 比如借 buffer 借器材08/28 07:40
20F→:pH 值有時候也會影響 如果 pH meter 不準的話08/28 07:41
2F→:改用低零敏度的 ECL08/15 00:00
3F→:或是降低二抗 titer08/15 00:01
13F→:pro- 跟 actived form 是同一支抗體嗎 如果是不同支抗體07/14 19:11
14F→:可能要調整一下抗體的 titer 如果是同支 通常 act-form 量少07/14 19:11
15F→:比較難壓出來 有圖可以給大家看會比較清楚是壓沒有還是反白07/14 19:12
6F→:會不均勻 每次做 擴散的程度會不一樣03/03 23:36
12F→:primer 被汙染了?03/03 23:38
1F→:濾紙+漏斗 不過要過很久02/28 15:18
2F→:但是就是接著血清瓶一直給它自己滴 過陣子再去補滿濾紙02/28 15:18
3F→:內的 Coomassie blue02/28 15:19
4F→:我覺得反應時間也有差02/22 00:54