作者查詢 / Ianthegood
作者 Ianthegood 在 PTT [ Biotech ] 看板的留言(推文), 共1561則
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2F→: sonication?04/27 00:21
6F推: 除非上2D不然我都寧願dialysis+amicon XD04/27 03:50
7F→: sds應該比較強, 1%不夠就2%, 但是你的protein就肯定04/27 03:51
8F→: 死光04/27 03:51
7F推: 樓上 通常這種抓下來會ligate上dna oilgo再pcr送ngs04/15 03:06
8F推: 兩種都有 現在也開始有系統生物學方法開始大規模看全04/15 03:08
9F→: 部的RNP04/15 03:08
10F推: beads最常見是coat streptavidin, magnetic只是方便你04/15 06:11
11F→: wash, 用一顆磁鐵就可以拉下來不用離心04/15 06:11
5F推: 表現量夠高 多過幾根column總是可以純化的 不過你要04/02 23:32
6F→: 建standard curve可能還是得要MS或AAA04/02 23:32
8F推: 樓上western跟elisa一樣 你得知道多少protein是多大04/03 15:47
9F→: 根的band才行04/03 15:47
20F推: 你買得到standard sample夠純就跑BCA就好啦 浪費兩個04/07 23:33
21F→: 小時跑elisa幹嘛 傻傻的04/07 23:33
22F→: 然後對啊買得到幹嘛自己純化04/07 23:33
4F推: 樓上科科03/28 19:24
13F推: 35mb超小 不是小細菌大病毒就是胞器吧 胞器會比較吃專03/28 22:55
14F→: 業 建議找做過的人來分析03/28 22:55
1F推: 推一個專業03/23 03:20
4F推: 最近有篇paper講pfa+一點點的gutaraldehyde效果更好03/24 18:30
5F→: 不過mitochondria大概沒差03/24 18:30
8F→: 這篇就是講和了pfa的ga沒什麼螢光 Huebinger 2018 sci03/25 06:07
9F→: entific reports03/25 06:07
8F推: 小弟跟動物細胞不熟, 2 formaldehyde的medium裡是有fb03/21 22:59
9F→: s的嗎?03/21 22:59
3F推: 是說就算有candidate gene要infer代謝物還是超難吧03/18 21:31
5F推: 有flow何必不用 手套不用泡 噴一噴就好 簽字筆就縫好03/13 19:13
6F→: 再寫囉03/13 19:13
7F推: 經驗中 水有訊號通常是污染03/11 16:53
8F推: 你的疑慮的確有重要性 但是以實用性考量現在還是以qPC03/11 16:56
9F→: R為主流 畢竟沒人有錢到什麼都打sequencing03/11 16:56
14F推: 回原po 對 Ct是ok的 然後樓上+1 通常水有訊號都是自己03/13 19:09
15F→: 手殘cross contaminate到03/13 19:09
16F→: 然後不只要看peak還要看強度 有時候只是noise03/13 19:10
8F推: 也有可能就是希望它不穩定 表現完就快閃 留個dsDNA在03/11 07:52
9F→: 那裡其實很麻煩的03/11 07:52