I wonder why some biologists use PIPES pH 8.0 in lysis buffers in Protocols?
whereas the buffering range of it is 6.1-7.5 pH.
You can find those protocols even in high rank universities.
2 replies to this topic
#1
Posted 01 September 2012 - 04:15 PM
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Babak Memari
Babak Memari
#2
Posted 03 September 2012 - 02:42 PM
buffers are routinely misused when the procedure works anyway (e.g. tris used for stacking gel buffers in sds-page).
however, sometimes buffers are blended to extend buffering range and/or to buffer a pH that would otherwise have to be reached with a incompatible buffer salt.
are there other buffer salts in your lysis media?
however, sometimes buffers are blended to extend buffering range and/or to buffer a pH that would otherwise have to be reached with a incompatible buffer salt.
are there other buffer salts in your lysis media?
Edited by mdfenko, 03 September 2012 - 02:43 PM.
talent does what it can
genius does what it must
i do what i get paid to do
genius does what it must
i do what i get paid to do
#3
Posted 03 September 2012 - 03:30 PM
Cell Lysis buffer
5 mM PIPES pH 8.0
85 mM KCL
0.5% NP40
protease inhibitors
http://farnham.genom...u/protocol.html
I have sent an Email to Dr. Farnham, and I did not received reply till now.
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Babak Memari
5 mM PIPES pH 8.0
85 mM KCL
0.5% NP40
protease inhibitors
http://farnham.genom...u/protocol.html
I have sent an Email to Dr. Farnham, and I did not received reply till now.
-----
Babak Memari
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Babak Memari
Babak Memari
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