Precipitation appears after adding sodium acetate but before adding cold ethanol
Started by fzhang, Sep 10 2009 01:31 AM
8 replies to this topic
#1
Posted 10 September 2009 - 01:31 AM
Hi, everyone. I am extracting some genomic DNA from some soil samples. But I found some white stuff in the bottom of the mirco tube imediately after adding NaAc to it, but I had not yet added cold ethanol. When I votex the tube, the white stuff disappeared.
Can anyone tell me how did this all come out?
Thanks.
Can anyone tell me how did this all come out?
Thanks.
#2
Posted 10 September 2009 - 04:04 PM
fzhang, on Sep 10 2009, 07:31 PM, said:
Hi, everyone. I am extracting some genomic DNA from some soil samples. But I found some white stuff in the bottom of the mirco tube imediately after adding NaAc to it, but I had not yet added cold ethanol. When I votex the tube, the white stuff disappeared.
Can anyone tell me how did this all come out?
Thanks.
Can anyone tell me how did this all come out?
Thanks.
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#3
Posted 10 September 2009 - 05:18 PM
fzhang, on Sep 10 2009, 04:31 AM, said:
Hi, everyone. I am extracting some genomic DNA from some soil samples. But I found some white stuff in the bottom of the mirco tube imediately after adding NaAc to it, but I had not yet added cold ethanol. When I votex the tube, the white stuff disappeared.
Can anyone tell me how did this all come out?
Thanks.
Can anyone tell me how did this all come out?
Thanks.
I have that happen as well. I don't know what the cause of it is. I do know that swirling or inverting it causes it to disappear.
#4
Posted 11 September 2009 - 08:16 AM
can anyone help?
#6
Posted 13 September 2009 - 09:30 PM
swanny, on Sep 14 2009, 01:18 PM, said:
After adding one volume of chloroform isoamyl alcohol (24:1) to my crude DNA solution, I pipette the upper aqueous phase to another tube. Then I added 0.1 volume of 3M sodium acetate to this solution. Right then some white stuff like precipiation appeared in the lower part of the volume. If I inverted the tube, this white stuff would readily vanish.
Thanks a lot, swanny.
#7
Posted 13 September 2009 - 10:50 PM
is your NaAcetate ice cold AND you are using CTAB in one of the previous steps? If yes: you should keep your samples on ice before removing the supernatant. CTAB preciptiates at low temps (lower than app. 10-15°C). Therefore it will vanish again, when warm enough.
Keeping you samples cold will allow you to remove the CTAB from your DNA...good for PCR, as CTAB is a strong inhibitor.
Keeping you samples cold will allow you to remove the CTAB from your DNA...good for PCR, as CTAB is a strong inhibitor.
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#8
Posted 14 September 2009 - 01:04 AM
gebirgsziege, on Sep 14 2009, 02:50 PM, said:
is your NaAcetate ice cold AND you are using CTAB in one of the previous steps? If yes: you should keep your samples on ice before removing the supernatant. CTAB preciptiates at low temps (lower than app. 10-15°C). Therefore it will vanish again, when warm enough.
Keeping you samples cold will allow you to remove the CTAB from your DNA...good for PCR, as CTAB is a strong inhibitor.
Keeping you samples cold will allow you to remove the CTAB from your DNA...good for PCR, as CTAB is a strong inhibitor.
Thanks. But neither did I use CTAB nor put my samples on the ice. It's wierd, right?
#9
Posted 14 September 2009 - 01:31 AM
lot of polysaccarides or glycoproteins?
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