Hi all,
I am extracting DNA from human blood cells using Qiagen Flexigene. However, at the end when I resuspend the DNA pellet using Qiagen's FG3 buffer (10mM Tris pH 8.5). The DNA seems do not dissolve well that I found the solution sticky/viscous.
And when I measure the DNA using nanodrop, it gives multiple concentrations upon several measurement. For example, in one measurement it gives 50ng/uL, in another measurement it gives 200ng/uL, several folds increase in concentration!!
Is there any suggestion for improvement and reason for this? Many thanks.
Protocol used:
Briefly, I used Qiagen Flexigene kit. cells were lysed by Qiagen protease. subsequently after lysis add isopropanol to precipitate DNA. Followed by I wash the DNA with 70% ethanol twice. Then resuspend the pellet in FG3 buffer (10mM Tris pH 8.5) after ethanol dry.
I am extracting DNA from human blood cells using Qiagen Flexigene. However, at the end when I resuspend the DNA pellet using Qiagen's FG3 buffer (10mM Tris pH 8.5). The DNA seems do not dissolve well that I found the solution sticky/viscous.
And when I measure the DNA using nanodrop, it gives multiple concentrations upon several measurement. For example, in one measurement it gives 50ng/uL, in another measurement it gives 200ng/uL, several folds increase in concentration!!
Is there any suggestion for improvement and reason for this? Many thanks.
Protocol used:
Briefly, I used Qiagen Flexigene kit. cells were lysed by Qiagen protease. subsequently after lysis add isopropanol to precipitate DNA. Followed by I wash the DNA with 70% ethanol twice. Then resuspend the pellet in FG3 buffer (10mM Tris pH 8.5) after ethanol dry.
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