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作者 nike77114 在 PTT [ Biotech ] 看板的留言(推文), 共180則
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4F→: 序列稀釋後得到一檢量線,針對該檢量線的Standard02/07 13:30
5F→: error算出數值,而後以斜率除以該se(Y)得到的數字乘上02/07 13:38
6F→: 3.3得到機器的LOD乘上10得到LOQ02/07 13:49
7F→: 而後把機器的LOQ作為樣品的添加濃度重複7次or以上02/07 13:50
8F→: 計算標準差(S),而後帶入LOD = t0.99 * S。t0.9902/07 13:51
9F→: 用excel =T.INV(0.99,df)計算就可以得到真實的LOD02/07 13:52
10F→: 乘上10就是LOQ了02/07 13:52
6F→: 基質不單純時請用標準添加法進行濃度測試02/07 13:27
7F→: 必要時請計算回收率02/07 13:27
11F推: 因為->芭芭拉·麥克林托克<-02/16 14:05
8F→:不是應該稀釋然後分裝用嗎@@?07/18 15:30
9F→:原PO是指其他人都直接取母液?07/18 15:30
1F→:35S promoter接PIF gene10/04 10:53
10F→:直接試試看只有Agar看看會不會凝?09/25 09:46
5F→:你可以先說看看蝦子的gDNA大小是多少?然後預期跑到哪阿05/28 09:00
4F推:insert上面選個切位,plasmid上面選個切位先確認05/09 08:50
3F→:我個人認為抽氣式沒有傳統好用XDDD05/06 21:13
1F→:濃度OK,純度如何呢?01/30 12:34
3F→:那是誰阿(咦01/30 16:21
4F→:不然就以Plasmid DNA然後抽多一點,用PCI純化01/30 16:23
5F→:濃度可以較高01/30 16:33