MOPS: Difference between revisions
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'''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. | '''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== | ==Recipe for 10x MOPS buffer== | ||
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* 41.2 g 3-(N-morpholino) propanesulfonic acid (MOPS); MW 209.3 g/mol | * 41.2 g 3-(N-morpholino) propanesulfonic acid (MOPS); MW 209.3 g/mol | ||
* 10.9 g Sodium Acetate, | * 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 | * 3.7 g EDTA, sodium salt; MW 292.2 g/mol | ||
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* protect from light; do not use if the solution appears yellow | * protect from light; do not use if the solution appears yellow | ||
==Final concentration of active compounds== | |||
==Final concentration of active compounds in 10x stock== | |||
* 400 mM MOPS (buffering) | * 400 mM MOPS (buffering) | ||
* 100 mM NaAc | * 100 mM NaAc | ||
* 10 mM [[EDTA]] (nuclease inhibition by Mg2+ chelation) | * 10 mM [[EDTA]] (nuclease inhibition by Mg2+ chelation) | ||
==Stability of MOPS== | ==Stability of MOPS== | ||
Contrary to common belief, MOPS is sufficiently heat-stable to be autoclaved. | 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 [http://books.google.de/books?id=h5lGFPz054oC&pg=PA201&dq=farrel+rna+mops&lr=&ei=RAGsSb_8NouYMp7enJIF&hl=en] | ||
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* [[Knight:NuPAGE electrophoresis]] | * [[Knight:NuPAGE electrophoresis]] | ||
* [[Sauer:bis-Tris SDS-PAGE, the very best]] | * [[Sauer:bis-Tris SDS-PAGE, the very best]] | ||
== External links == | == External links == | ||
* [http://en.wikipedia.org/wiki/MOPS Wikipedia MOPS] | * [http://en.wikipedia.org/wiki/MOPS Wikipedia MOPS] | ||
Revision as of 09:31, 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
