作者查詢 / leondemon
作者 leondemon 在 PTT [ Biotech ] 看板的留言(推文), 共55則
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6F→:我說的髒是背景很髒~04/01 21:39
20F推:推satasumi 超高量定序機器比real-time PCR好太多了10/14 11:01
2F→:謝謝你 這我有看過了 但是沒有得到解答耶 ^^"10/07 23:02
3F→:目前我有找到資料寫可以兩端定序 大約36bp左右10/07 23:03
4F→:但是每個如何移除那個fluorophore 則不知道10/07 23:04
5F→:那個特殊核甘酸結構還是未知 只知道是有屬於私有財產10/07 23:05
17F→:sGoat會不會把Solexa講的太神了呀?10/08 13:49
18F→:另外回kitty 專利的東西在申請的時候必須要講清楚10/08 13:52
19F→:我找到資料對於該核甘酸的技術 是用私有財產的字眼10/08 13:52
20F→:所以很有可能沒有申請專利 只是沒人能知道那是什麼原理10/08 13:53
21F→:Solexa最主要是能夠一次定序5千萬種不同的DNA分子10/08 13:57
22F→:每個分子只要定序一端20個以上nt 就可以產生unique tag10/08 13:58
23F→:再去比對基因體序列資料庫 就知道這片段來自哪裡10/08 13:59
24F→:我目前看到介紹好像是可以一邊定序到36nt 可能不是極限10/08 14:00
25F→:所以一次可以定1.5 Gbp 若是兩邊定序可達3 Gbp10/08 14:01
26F→:他每bp定序是一個cycle 光要掃描5千萬colony就要很久10/08 14:03
27F→:掃完後 不知道是用什麼chemistry 將block的fluorophore10/08 14:04
28F→:自核甘酸尾巴移除 然後可以進行下一個cycle10/08 14:04
29F→:但是木前就是找不到那個特殊修飾核甘酸的結構和原理是啥10/08 14:05
48F→:還是很謝謝sGoat大的資訊 另外也謝謝cryo大的分享10/09 00:08
49F→:我原本想說36個cycle還要用天數來算 以為是用scanning10/09 00:12
50F→:CCD camera方式的確是聰明許多10/09 00:12
51F→:果然還是需要討論才知道自己哪裡理解錯誤 謝謝大家啦~10/09 00:13
52F→:簡單來說 那個特殊核甘酸應該是把螢光劑接在3'端10/09 00:35
53F→:可終止elongation 但是用特殊方法移除後 又可添加1 nt10/09 00:35
54F→:這樣講應該對吧!?10/09 00:36
8F推:淚推2F09/27 02:03
1F推:感謝 Q.Q06/30 21:02
3F→:謝謝06/25 13:57
3F→:感謝提供!很有助益 :) 但是我想多知道關於我上面敘述的06/18 14:57
3F推:蠻好奇滅菌是為了什麼? 又不是拿來加入培養基 為何滅菌06/14 13:16
4F→:市面賣Triton大多是Protease/Nuclease free的分生試劑06/14 13:18
1F推:這是一個很好的建議06/14 21:04
1F推:給個推~!12/22 01:04