作者查詢 / FireHell
作者 FireHell 在 PTT 全部看板的留言(推文), 共2023則
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6F→:據說是因為細胞特性不同,造成一樓所說,所以CONTROL也會03/27 03:24
1F推:這程式本來就很不準ˊˋ03/27 03:21
12F推:請問5841是哪裡的價格啊?03/28 00:26
1F推:沒錯就是因為有SERUM的關係03/14 17:49
2F→:http://www.ncbi.nlm.nih.gov/pubmed/2012398903/14 17:49
3F→:建議改用low serum (0.5-2%)03/14 17:50
5F推:沒有設計主題,真可惜03/14 01:29
3F推:沒做過IP,不過WB的經驗告訴我抗體的特異性其實很不特異03/12 01:27
4F→:XD03/12 01:27
5F推:加到MEDIUM後會大量稀釋,通常都可溶03/07 21:31
6F→:但可能會因局部濃度過高而產生結晶,因此要先pipetting03/07 21:32
7F→:注意pipetting時不可有細胞03/07 21:32
1F推:清除快取COOKIE後重新抓檔去修改02/29 13:13
1F推:參數跑掉了02/28 02:34
3F推:FSC, SSC, FL2, FL2-A, FL2-W這些參數的Voltage和amp02/29 13:06
4F→:要調一下02/29 13:06
5F→:另外橢圓形和帶狀都是正常的耶02/29 13:08
21F→:不同時間點的FSC和SSC可以參數不同,GATING範圍不同03/01 14:15
22F→:看起來比較像是細胞型態在48H後劇烈變化而沒有GATING好03/01 14:16
23F→:另外一個可能就是你的TREAT會導致S phase arrest03/01 14:17
34F推:收細胞要快,所以放1h絕對不ok,不過會不會導致這些結果03/02 15:12
35F→:不得而知,建議下次收細胞要連續之外,可參照這篇03/02 15:12
36F→:http://0rz.tw/wAduL03/02 15:13
37F→:另外注意流速控制在LOW SPEED 100 EVENTS/SEC03/02 15:15
2F→:先用低電壓讓它通過上膠後再調高至所需電壓02/28 02:35
15F→:要用5X dye和ddwater稀釋到濃度相同,體積才會一樣02/29 13:09