Thanks.
Working with DNA, RNA and oligonucleotides
Started by seasons, Mar 24 2005 04:56 AM
5 replies to this topic
#1
Posted 24 March 2005 - 04:56 AM
Should i always work my DNA, RNA and oligonucleotides on ice or can i also work with them in room temperatures?
Thanks.
Thanks.
#2
Posted 24 March 2005 - 06:27 AM
hi
ALWAYS work seems quite strong, but i work as many as possible on ice.
ALWAYS work seems quite strong, but i work as many as possible on ice.
#3
Posted 24 March 2005 - 07:17 AM
fred_33, on Mar 24 2005, 07:27 AM, said:
What is the reasons for that or does this depend on the protocol? The DNA in the cells in our body does not need ice.
Thanks.
#4
Posted 24 March 2005 - 09:13 AM
rnas are very sensitive pieces. So always work in ice with them.
For primers, i think it's better to defrost them slowly on ice to avoid degradaztion. But after, as you'"re relatively quick, no problem to be at RT.
For DNA, it's also quite sensitive material. Hence i thaw it on ice and try to work in ice.
In cells there is plenty of dna repair porteins (why i am not one?
), and dna is well stabilized
For primers, i think it's better to defrost them slowly on ice to avoid degradaztion. But after, as you'"re relatively quick, no problem to be at RT.
For DNA, it's also quite sensitive material. Hence i thaw it on ice and try to work in ice.
In cells there is plenty of dna repair porteins (why i am not one?
#5
Posted 27 March 2005 - 06:37 PM
Hi,
For DNA and primers, there is no a big problem even if you forget them overnight at RT° once, twice but not forever or often!!!
For RNA, which is more sensitive to be degraded by the omnipresent RNase, it's necessary to keep them in ice !!
good luck
for
For DNA and primers, there is no a big problem even if you forget them overnight at RT° once, twice but not forever or often!!!
For RNA, which is more sensitive to be degraded by the omnipresent RNase, it's necessary to keep them in ice !!
good luck
fred_33, on Mar 24 2005, 10:13 AM, said:
rnas are very sensitive pieces. So always work in ice with them.
For primers, i think it's better to defrost them slowly on ice to avoid degradaztion. But after, as you'"re relatively quick, no problem to be at RT.
For DNA, it's also quite sensitive material. Hence i thaw it on ice and try to work in ice.
In cells there is plenty of dna repair porteins (why i am not one?
), and dna is well stabilized
For primers, i think it's better to defrost them slowly on ice to avoid degradaztion. But after, as you'"re relatively quick, no problem to be at RT.
For DNA, it's also quite sensitive material. Hence i thaw it on ice and try to work in ice.
In cells there is plenty of dna repair porteins (why i am not one?
for
#6
Posted 31 March 2005 - 10:31 AM
hi
its better to work on ice specially i u r alow worker and take alot of Time to prepare PCR mixtures
u can leave primers to thaw slowely on ice ,,,and work with them in room temperature then freez them again ,but u better avoid this in RNA as its very sensetive
its better to work on ice specially i u r alow worker and take alot of Time to prepare PCR mixtures
u can leave primers to thaw slowely on ice ,,,and work with them in room temperature then freez them again ,but u better avoid this in RNA as its very sensetive
Edited by lula, 31 March 2005 - 10:35 AM.














