MOPS: Difference between revisions
From OpenWetWare
Jump to navigationJump to search
No edit summary |
|||
Line 41: | Line 41: | ||
== External links == | == External links == | ||
* [http://en.wikipedia.org/wiki/MOPS Wikipedia MOPS] | * [http://en.wikipedia.org/wiki/MOPS Wikipedia MOPS] | ||
* [http://cshprotocols.cshlp.org/cgi/content/full/2006/3/pdb.rec8332?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&fulltext=mops&searchid=1&FIRSTINDEX=0&resourcetype=HWCIT&text_only=true CSH Protocols MOPS] [[Image:Padlock-closed.png]] |
Revision as of 09:39, 2 March 2009
MOPS is the common name for the buffering compound in MOPS buffer. MOPS stands for 3-(N-morpholino) propanesulfonic acid and with a pKa of 7.20, MOPS is an good buffer for many biological systems at almost neutral pH. HEPES is a chemically similar pH buffering compound.
Recipe for 10x MOPS buffer
- 41.2 g 3-(N-morpholino) propanesulfonic acid (MOPS); MW 209.3 g/mol
- 10.9 g Sodium Acetate, trihydrate; MW 136.1 g/mol (watch out: NaAc, anhydrous is lighter with MW = 82 g/mol)
- 3.7 g EDTA, sodium salt; MW 292.2 g/mol
- add 800 ml of nuclease free distilled water; mix to dissolve
- adjust to pH 7 with NaOH (prepared in nuclease free distilled water)
- fill to the final volume of 1000 ml
- filter sterilise or autoclave
- store at room temperature
- protect from light; do not use if the solution appears yellow
Final concentration of active compounds in 10x stock
- 400 mM MOPS (buffering)
- 100 mM NaAc
- 10 mM EDTA (nuclease inhibition by Mg2+ chelation)
Stability of MOPS
Contrary to common belief, MOPS is sufficiently heat-stable to be autoclaved. Solution will turn yellow but this does not interfere with its buffering capacity. See, for example, Farrell RNA methods, p201 [1]
Some OWW protocols which use MOPS
- Jacobs:Protocol RNA Agarose Gel
- Knight:NuPAGE electrophoresis
- Sauer:bis-Tris SDS-PAGE, the very best