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Difference between revisions of "MiPNet14.13 Medium-MiR06"

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{{OROBOROS header page name}}
{{Publication
{{Publication
|title=Fasching M, Eigentler A, Fontana-Ayoub M, Gnaiger E. Mitochondrial respiration medium - MiR06. Mitochondr Physiol Network 14.13.
 
|info=[http://www.oroboros.at/?Protocols_MiR06 MiPNet14.13 Open Access]
|title=[[Image:O2k-Protocols.jpg|right|80px|link=http://wiki.oroboros.at/index.php/O2k-Protocols|O2k-Protocols]] Mitochondrial respiration medium - MiR06.
|authors=OROBOROS
|info=[[File:PDF.jpg|100px|link=http://wiki.oroboros.at/images/d/d9/MiPNet14.13_Medium-MiR06.pdf |Bioblast pdf]] »[http://www.bioblast.at/index.php/File:MiPNet14.13_Medium-MiR06.pdf Versions]
|year=*
|authors=Oroboros
|year=2016-08-30
|journal=Mitochondr Physiol Network
|journal=Mitochondr Physiol Network
|abstract=Mitochondrial respiration medium 06, developed for oxygraph incubations of mitochondrial preparations = MiR05 plus catalase.
|abstract='''Fasching M, Fontana-Ayoub M, Gnaiger E (2018) Mitochondrial respiration medium - MiR06. Mitochondr Physiol Network 14.13(06):1-4.'''
{{MiPNet pdf page linking to MitoPedia}}
 
Mitochondrial respiration medium MiR06 was developed for oxygraph incubations of mitochondrial preparations. MiR06 = MiR05 plus catalase. MiR06Cr = MiR06+creatine.
 
:» Product: [[MiR05-Kit]]
|keywords=MiR06
|keywords=MiR06
|mipnetlab=AT_Innsbruck_OROBOROS
|mipnetlab=AT_Innsbruck_Oroboros
|articletype=Protocol; Manual, MiPNet-online Publication
|discipline=Mitochondrial Physiology
}}
}}
{{Labeling
{{Labeling
|area=Instruments and methods
|area=Instruments;methods
|instruments=Protocol
|instruments=O2k-Protocol
|additional=Chemicals & Media
|additional=O2k-chemicals and media
|articletype=Protocol; Manual, MiPNet-online Publication
|discipline=Mitochondrial Physiology
}}
}}
__TOC__
== Application of MiR06 in [[HRR]] ==
== Application of MiR06 in [[HRR]] ==


'''MiR06: Mitochondrial Respiration Medium''' ([[#Preparation of MiR05 (MiR06) stock solution|MiR06]] = [[MiR05]] + [[Catalase]]). Total volume = 1 litre.
'''MiR06: Mitochondrial Respiration Medium''' ([[#Preparation of MiR05 (MiR06) stock solution|MiR06]] = [[MiR05]] + [[Catalase]]).


::Oxygen solubility factor in MiR05 or MiR06 at 30°C and 37°C = 0.92
::Oxygen solubility factor in MiR05 or MiR06 at 30 °C and 37 °C = 0.92


::pH of MiR05/06: 7.2 (20°C), 7.2 (25°C), 7.1 (30°C), 7.1 (35°C), 7.0 (37°C)
::pH of MiR05/06: 7.2 (20 °C), 7.2 (25 °C), 7.1 (30 °C), 7.1 (35 °C), 7.0 (37 °C)




== Re-oxygenation with H2O2 titrations ==
== Re-oxygenation ==


* '''To increase oxygen levels''' small volumes (µl) of [[#Preparation of 200 mM H2O2 stock solution|200 mM H<sub>2</sub>O<sub>2</sub> stock concentration]] are injected into the O2k-chamber filled with MiR06.
::An experiment needs not necessarily be terminated, because of running out of oxygen. There are different ways to re-oxygenate. See all of them in [[Setting the oxygen concentration]]


With MiR06 (or [[MiR06Cr]]), the medium in the O2k-chamber can be re-oxygenated very conveniently with H<sub>2</sub>O<sub>2</sub> titrations. The initial increase in oxygen, however, is preferentially made with oxygen gas, since there is the risk of bubble formation if the oxygen concentration is increased in a single large step. If oxygen gas is not available  for initial oxygenation, a very small bubble may be left in the chamber while slowly rising the oxygen level to 500 µM with additions of H<sub>2</sub>O<sub>2</sub>, such that gas can escape into the small bubble and then be extruded by fully closing the chamber. During the experiment, re-oxygenations are sufficiently small such that H<sub>2</sub>O<sub>2</sub> into the closed chamber do not lead to gas bubble formation.
== Preparation of MiR05 (MiR06) stock solution ==
* Total volume of [[solution]] = 1 litre.
::1) Weigh given amounts of the [[Media:MiPNet14.13 Medium-MiR06.pdf| listed chemicals]] (except BSA and lactobionic acid) and transfer to a 1000 mL glass beaker.
::2) Disrupt big lumps mechanically. It is recommended to do this before adding water, because during dissolution these lumps do not disintegrate easily.
::3) Add ~800 mL H<sub>2</sub>O and dissolve using a magnetic stirrer at ~30 °C
::4) Add 120 mL of [[#Preparation of K-lactobionate stock solution|K-lactobionate stock solution]].
::5) Adjust the pH to 7.1 with 5 M KOH at 30 °C.
::6) Dissolve the BSA in a subsample of the MiR05 stock solution and add to the final MiR05 (the separate preparation of the BSA solution is recommended, since BSA produces foams that do not dissolve easily).
::7) Add H<sub>2</sub>0 to a final volume of 1000 mL.
::8) Check pH again and adjust if necessary with small volumes of 5 M KOH. This solution is '''MiR05'''. MiR05 can be stored at -20 °C as described for MiR06.
::9) To prepare <span style="color:#2E8B57"> '''MiR06'''</span>, add 280 000 units of catalase (100 mg of catalase powder containing 2800 U/mg solid) per litre MiR05 (280 units / mL final concentration).
::10) Divide into 40 mL portions in plastic vials and store at -20 °C.
::11) These storage solutions of MiR06 can be used as stock [[solution]]s. A vial is warmed up above experimental temperature, avoiding foam formation during gentle shaking. Up to 16 O2k-chambers can be filled with a 40 mL portion. It is recommended to use the stock solution on a single day only, to avoid any microbial contamination of the respiration medium.


::<span style="color:#2E8B57"> '''MiR06''' </span> can also be prepared by adding 5 µL of the [[#Preparation of catalase stock solution|catalase stock solution]] directly into the O2k-chamber filled with MiR05 at the start of the experiment. The final catalase concentration in the 2 mL O2k chamber is 280 U/mL.


== Preparation of MiR05 (MiR06) stock solution ==
=== Preparation of K-lactobionate stock solution ===


::1) weigh given amounts of the [[#Chemicals for MiR05|listed chemicals]] (except BSA and lactobionic acid) and transfer to a 1000 ml glass beaker
::1) weigh 35.83 g lactobionic acid into a 250 mL glass beaker
::2) disrupt big lumps mechanically. It is recommended to do this before adding water, because during dissolution these lumps do not disintegrate easily.
::2) add 100 mL H<sub>2</sub>O and dissolve by stirring on magnetic stirrer
::3) add ~800 ml H<sub>2</sub>O and dissolve on a magnetic stirrer at ~30 °C
::2) check pH (is approx. 2.0) and neutralize with 5 M KOH
::4) add 120 ml of [[#Preparation of K-lactobionate stock solution|K-lactobionate stock solution]]
::4) adjust final volume to 200 mL with H<sub>2</sub>O. It is best to use a 200 mL volumetric glass flask.
::5) adjust the pH to 7.1 with 5 N KOH at 30 °C
::5) check pH again and adjust to 7 if necessary (5 M KOH)
::6) transfer the MiR05 stock solution to a 1000 ml volumentric glass flask and add H20 to a final volume of 1000 ml <span style="color:#43CD80"> = '''MiR05''' </span>
::7) check pH again and adjust if necessary with small amounts of 5 N KOH
::8) dissolve the BSA in a subsample of the MiR05 stock solution and add to the final MiR05 (the separate preparation of the BSA solution is recommended, since BSA produces foams that do not dissolve easily)
::9) to prepare <span style="color:#2E8B57"> '''MiR06'''</span>, add 280 000 units of catalase (100 mg of catalase powder containing 2800 u/mg solid) per 1 L MiR05 (280 units / ml final concentration)
::10) divide into 40 ml portions and store at -20 °C in plastic vials


::<span style="color:#2E8B57"> '''MiR06''' </span> can also be prepared by adding 5 µl of the [[#Preparation of catalase stock solution|catalase stock solution]] directly into the O2k-chamber filled with MiR05 at the start of the experiment. The final catalase concentration in the 2 ml Oxygraph-2k chamber = 280 u/ml.
=== Preparation of catalase stock solution ===


::'''Catalase''' lypophilized powder, 2000-5000 '''Units*'''/mg, Sigma C 9322, store at -20 °C


==== Chemicals for MiR05/MiR06 ====
::'''Stock solution:''' 112000 U/mL (dissolved in MiR05)


<span style="color:#8B008B"> '''Caution:''' Chemicals stored in the fridge or freezer should be allowed to reach room temperature before opening.</span>
{|border="1" cellpadding="3" cellspacing="0"
|+
!Compound
!Final conc.
!FW
!Addition to 1 litre final volume
!Company, product code and storage
|-
|align="right"|EGTA
|align="right"|0.5 mM
|align="right"|380.4
|align="right"|0.190 g
|align="right"|Sigma E 4378, 25 g, store at R.T.
|-
|align="right"|MgCl<sub>2</sub>.6H<sub>2</sub>0
|align="right"|3 mM
|align="right"|203.3
|align="right"|0.610 g
|align="right"|Scharlau MA 0036, 250 g, store at R.T.
|-
|align="right"|Taurine
|align="right"|20 mM
|align="right"|125.1
|align="right"|2.502 g
|align="right"|Sigma T 0625, 25 g, store at R.T.
|-
|align="right"|KH<sub>2</sub>PO<sub>4</sub>
|align="right"|10 mM
|align="right"|136.1
|align="right"|1.361 g
|align="right"|Merck 104873, 1000 g, store at R.T.
|-
|align="right"|HEPES
|align="right"|20 mM
|align="right"|238.3
|align="right"|4.77 g
|align="right"|Sigma H 7523, 250 g, store at R.T.
|-
|align="right"|D-Sucrose
|align="right"|110 mM
|align="right"|342.3
|align="right"|37.65 g
|align="right"|Roth, 4621.1, 1000 g, store at R.T.
|-
|align="right"|BSA essentially fatty acid free
|align="right"|1 g/l
|align="right"|
|align="right"|1 g
|align="right"|Sigma A 6003 fraction V, 25 g, store at 2-8 °C
|-
|align="right"|Lactobionic acid
|align="right"|60 mM
|align="right"|358.3
|align="right"|120 ml of 0.5 M [[#Preparation of K-lactobionate stock solution|K-lactobionate stock]]
|align="right"|Aldrich 153516 or Sigma L2398, 100 g, store at R.T.
|-
|}


::'''Example:''' 'Catalase lypophilized powder, 2800 Units/mg solid and 3500 Units/mg protein'
==== Preparation of K-lactobionate stock solution ====


::1) weigh 35.83 g lactobionic acid into a 250 ml glass beaker
::1) Use 'Units/mg solid' for your calculations
::2) add 100 ml H<sub>2</sub>O and dissolve by stirring on magnetic stirrer
::2) Result: 40 mg catalase powder (2800 U/mg) are dissolved in 1 mL MiR05 to obtain a catalase stock solution with 112000 U/mL.
::2) check pH (is approx. 2.0) and neutralize with 5 N KOH
::3) Titrate 5 µL of the catalase stock solution into the 2 mL chamber to achieve a final concentration of 280 U/mL in the chamber.
::4) adjust final volume to 200 ml with H<sub>2</sub>O. It is best to use a 200 ml volumetric glass flask.
::5) check pH again and adjust to 7 if necessary (5 N KOH)


'''Unit definition:''' '''* Units''' of enzymatic activitiy (U) in µmol/min; assay used by Sigma Aldrich: ' ''One unit will decompose 1.0 μmol of H<sub>2</sub>O<sub>2</sub>  per min at pH 7.0 at 25 °C, while the H<sub>2</sub>O<sub>2</sub> concentration falls from 10.3 to 9.2 mM, measured by the rate of decrease of A<sub>240</sub>.'' '


=== Preparation of catalase stock solution ===
== MiR05Cr/MiR06Cr ==
* [[MiR05Cr]] = MiR05 + Creatine
* [[MiR06Cr]] = MiR06 + Creatine


::'''Catalase''' lypophilized powder, 2000-5000 '''units*'''/mg, Sigma C 9322, store at -20 °C
::1) Prepare fresh by adding 3 mg/mL creatine monohydrate (Fluka 27900, 100 g) to MiR05 or MiR06.
::2) Stirr gently on a magnetic stirrer.
::3) Do not freeze to avoid precipitation.


::'''Stock solution:''' 112000 u/ml (dissolved in MiR05)
== Preparation of H<sub>2</sub>O<sub>2</sub> stock solutions ==


:::: '''H<sub>2</sub>O<sub>2</sub>''': Hydrogen peroxide solution, 50 wt. % in H<sub>2</sub>O, stabilized, Sigma 516813, store in the fridge. See [http://www.h2o2.com/technical-library/default.aspx?pid=66&name=Safety-amp-Handling this link] for handling and safety instructions concerning hydrogen peroxide.


::'''Example:''' 'Catalase lypophilized powder, 2800 units/mg solid and 3500 units/mg protein'


::1) Use 'units/mg solid' for your calculations
:::: '''Preparation of 200 mM stock solution''' (dissolved in H<sub>2</sub>O) for '''2-mL O2k-chamber''':
::2) Result:  40 mg catalase powder (2800 u/mg) are dissolved in 1 ml MiR05 to obtain a catalase stock solution with 112000 u/ml.
::3) Titrate 5 µl of the catalase stock solution into the 2 ml chamber to achieve a final concentration of 280 IU/ml in the chamber.


'''Unit definition:''' '''* Units''' of enzymatic activitiy (u) in µmol/min; assay used by Sigma Aldrich: ' ''One unit will decompose 1.0 μmole of H<sub>2</sub>O<sub>2</sub> per min at pH 7.0 at 25 °C, while the H<sub>2</sub>O<sub>2</sub> concentration falls from 10.3 to 9.2 mM, measured by the rate of decrease of A<sub>240</sub>.'' '
::::# Pipette 114 µL of 17.6 M H<sub>2</sub>O<sub>2</sub> into 10 mL plastic vial.
::::# Add H<sub>2</sub>O, acidify with HCl (1 mM) to pH 6, complete with H<sub>2</sub>O to a total volume of 10 mL. Maintain the pH in the stock solution acidic to minimize autoxidation.
::::# Wrap plastic vial in aluminum foil (solution is light-sensitive) and store at 4 °C.
::::# During experiments keep the stock solution on ice.
:::»'''O2k manual titrations:''' [[MiPNet09.12]]


::::* Titration volume ('''2-mL O2k-chamber'''): 1-3 µL using a 10 µL Hamilton syringe.
::::* 3 µL of H<sub>2</sub>O<sub>2</sub> into the 2-mL O2k-chamber increases the concentration of O<sub>2</sub> by approx. 150 nmol/mL (150 µM).


=== Preparation of 200 mM H2O2 stock solution ===


'''H<sub>2</sub>O<sub>2</sub>''': Hydrogen peroxide solution, 50 wt. % in H2O, stabilized, Sigma 516813, store in the fridge, please see e.g. [http://www.solvayasiapacific.com/static/wma/pdf/1/8/5/8/1/Hydrogen%20Peroxide%20Handling%20%20Storage%201%28English%20version%29.pdf  this link] for handling and savety instructions concerning hydrogen peroxide.
:::: '''Preparation of 50 mM stock solution''' (dissolved in H<sub>2</sub>O) for '''0.5-mL O2k-chamber''':


::1) pipette 114 µl of 17.6 M H<sub>2</sub>O<sub>2</sub> into 10 ml plastic vial
::::# Pipette 28 µL of 17.6 M H<sub>2</sub>O<sub>2</sub> into 10 mL plastic vial.
::2) add H<sub>2</sub>O to a total volume of 10 ml
::::# Add H<sub>2</sub>O, acidify with HCl (1 mM) to pH 6, complete with H<sub>2</sub>O to a total volume of 10 mL. Maintain the pH in the stock solution acidic to minimize autoxidation.
::3) wrap plastic vial in aluminium foil (solution is light sensitive) and store in the fridge
::::# Wrap plastic vial in aluminum foil (solution is light-sensitive) and store at 4 °C.
::4) during experiments keep the solution on ice
::::# During experiments keep the stock solution on ice.
:::»'''O2k manual titrations:''' [[MiPNet09.12]]


'''titration''' of 3 µl of H<sub>2</sub>O<sub>2</sub> into 2 ml chamber would increase the concentration of O<sub>2</sub> by approx. 150 nmol/ml
::::* Titration volume ('''0.5-mL O2k-chamber'''): 1-3 µL using a 10 µL Hamilton syringe.
::::* 3 µL of H<sub>2</sub>O<sub>2</sub> into the 2-mL O2k-chamber increases the concentration of O<sub>2</sub> by approx. 150 nmol/mL (150 µM).


'''For detailed information on chemicals see [http://www.oroboros.at/index.php?protocols_miro6 MiPNet14.13].'''
<!--
'''Titration''' of 3 µL of H<sub>2</sub>O<sub>2</sub> into the 2-mL O2k-chamber increases the concentration of O<sub>2</sub> by approx. 150 nmol/mL (150 µM).-->


== MiR06Cr ==
== Limitations of using MiR media ==


* [[MiR06Cr]] = MiR06 + Creatine
::* MiR06 or MiR06Cr cannot be used for measurement of ROS production. Use MiR05 or MiR05Cr instead.
::* The high antioxidant activity may compete with reactions on which measurement of ROS production is based.
::* The intracellular milieu of kidney has a low [K<sup>+</sup>]. Kidney mitochondria are inhibited by the high [K<sup>+</sup>] of MiR05 to MiR06Cr [1].
>> [[MiPMap#1._Human_and_model_organisms.2C_taxonomic_groups|MiPMap -  Is this a general issue for the organ, or is it in addition also a species issue?]]


::1) prepare every morning fresh by adding 3 mg/mL creatine monohydrate (Fluka 27900) to [[MiR06]]
# A mitochondrial respiration medium for kidney: [[Friederich-Persson 2012 Diabetologia]].
::2) stirr gently on a magnetic stirrer


== Limitations of using MiR05 to MiR06Cr ==
== Further information ==
 
::* [[MiPNet06.03_O2-Calibration-Solubility |Oxygen solubility in MiR06]]
* The high antioxidant activity may interfere with the measurement of ROS production.
* The intracellular milieu of kidney has a low [K<sup>+</sup>]. Kidney mitochondria are inhibited by the high [K<sup>+</sup>] of MiR05 to MiR06Cr [1].
>> [[MiPMap#1._Human_and_model_organisms.2C_taxonomic_groups|MiPMap -  Is this a general issue for the organ, or is it in addition also a species issue?]]


# Reference on a mitochondrial respiration medium for kidney: [[Persson_2012_Diabetologia]].
::* [[MitoPedia: Media for respirometry]]


::* MiPNet08.05 and MiPNet10.11 are integrated in MiPNet14.13_Medium-MiR06.


MiPNet10.11 is integrated in MiPNet14.13_Medium-MiR06.
'''Original publication introducing MiR05:'''
* [[Gnaiger 2000 Life in the Cold|Gnaiger E, Kuznetsov AV, Schneeberger S, Seiler R, Brandacher G, Steurer W, Margreiter R (2000) Mitochondria in the cold. In: Life in the Cold (Heldmaier G, Klingenspor M, eds) Springer, Heidelberg, Berlin, New York: pp 431-442.]]

Latest revision as of 10:25, 16 March 2022

                



MiPNet14.13 Medium-MiR06


Publications in the MiPMap
O2k-Protocols
Mitochondrial respiration medium - MiR06.

» Bioblast pdf »Versions

Oroboros (2016-08-30) Mitochondr Physiol Network

Abstract: Fasching M, Fontana-Ayoub M, Gnaiger E (2018) Mitochondrial respiration medium - MiR06. Mitochondr Physiol Network 14.13(06):1-4.

O2k-technical support and open innovation
Open the pdf document above.
» Current O2k-series: NextGen-O2k Series XB and O2k Series J
» Current software versions DatLab 8.0: MitoPedia: DatLab

Mitochondrial respiration medium MiR06 was developed for oxygraph incubations of mitochondrial preparations. MiR06 = MiR05 plus catalase. MiR06Cr = MiR06+creatine.

» Product: MiR05-Kit

Keywords: MiR06

O2k-Network Lab: AT_Innsbruck_Oroboros


Labels: MiParea: Instruments;methods 





HRR: O2k-Protocol 

O2k-chemicals and media 

Application of MiR06 in HRR

MiR06: Mitochondrial Respiration Medium (MiR06 = MiR05 + Catalase).

Oxygen solubility factor in MiR05 or MiR06 at 30 °C and 37 °C = 0.92
pH of MiR05/06: 7.2 (20 °C), 7.2 (25 °C), 7.1 (30 °C), 7.1 (35 °C), 7.0 (37 °C)


Re-oxygenation

An experiment needs not necessarily be terminated, because of running out of oxygen. There are different ways to re-oxygenate. See all of them in Setting the oxygen concentration

Preparation of MiR05 (MiR06) stock solution

1) Weigh given amounts of the listed chemicals (except BSA and lactobionic acid) and transfer to a 1000 mL glass beaker.
2) Disrupt big lumps mechanically. It is recommended to do this before adding water, because during dissolution these lumps do not disintegrate easily.
3) Add ~800 mL H2O and dissolve using a magnetic stirrer at ~30 °C
4) Add 120 mL of K-lactobionate stock solution.
5) Adjust the pH to 7.1 with 5 M KOH at 30 °C.
6) Dissolve the BSA in a subsample of the MiR05 stock solution and add to the final MiR05 (the separate preparation of the BSA solution is recommended, since BSA produces foams that do not dissolve easily).
7) Add H20 to a final volume of 1000 mL.
8) Check pH again and adjust if necessary with small volumes of 5 M KOH. This solution is MiR05. MiR05 can be stored at -20 °C as described for MiR06.
9) To prepare MiR06, add 280 000 units of catalase (100 mg of catalase powder containing 2800 U/mg solid) per litre MiR05 (280 units / mL final concentration).
10) Divide into 40 mL portions in plastic vials and store at -20 °C.
11) These storage solutions of MiR06 can be used as stock solutions. A vial is warmed up above experimental temperature, avoiding foam formation during gentle shaking. Up to 16 O2k-chambers can be filled with a 40 mL portion. It is recommended to use the stock solution on a single day only, to avoid any microbial contamination of the respiration medium.
MiR06 can also be prepared by adding 5 µL of the catalase stock solution directly into the O2k-chamber filled with MiR05 at the start of the experiment. The final catalase concentration in the 2 mL O2k chamber is 280 U/mL.

Preparation of K-lactobionate stock solution

1) weigh 35.83 g lactobionic acid into a 250 mL glass beaker
2) add 100 mL H2O and dissolve by stirring on magnetic stirrer
2) check pH (is approx. 2.0) and neutralize with 5 M KOH
4) adjust final volume to 200 mL with H2O. It is best to use a 200 mL volumetric glass flask.
5) check pH again and adjust to 7 if necessary (5 M KOH)

Preparation of catalase stock solution

Catalase lypophilized powder, 2000-5000 Units*/mg, Sigma C 9322, store at -20 °C
Stock solution: 112000 U/mL (dissolved in MiR05)


Example: 'Catalase lypophilized powder, 2800 Units/mg solid and 3500 Units/mg protein'
1) Use 'Units/mg solid' for your calculations
2) Result: 40 mg catalase powder (2800 U/mg) are dissolved in 1 mL MiR05 to obtain a catalase stock solution with 112000 U/mL.
3) Titrate 5 µL of the catalase stock solution into the 2 mL chamber to achieve a final concentration of 280 U/mL in the chamber.

Unit definition: * Units of enzymatic activitiy (U) in µmol/min; assay used by Sigma Aldrich: ' One unit will decompose 1.0 μmol of H2O2 per min at pH 7.0 at 25 °C, while the H2O2 concentration falls from 10.3 to 9.2 mM, measured by the rate of decrease of A240. '

MiR05Cr/MiR06Cr

1) Prepare fresh by adding 3 mg/mL creatine monohydrate (Fluka 27900, 100 g) to MiR05 or MiR06.
2) Stirr gently on a magnetic stirrer.
3) Do not freeze to avoid precipitation.

Preparation of H2O2 stock solutions

H2O2: Hydrogen peroxide solution, 50 wt. % in H2O, stabilized, Sigma 516813, store in the fridge. See this link for handling and safety instructions concerning hydrogen peroxide.


Preparation of 200 mM stock solution (dissolved in H2O) for 2-mL O2k-chamber:
  1. Pipette 114 µL of 17.6 M H2O2 into 10 mL plastic vial.
  2. Add H2O, acidify with HCl (1 mM) to pH 6, complete with H2O to a total volume of 10 mL. Maintain the pH in the stock solution acidic to minimize autoxidation.
  3. Wrap plastic vial in aluminum foil (solution is light-sensitive) and store at 4 °C.
  4. During experiments keep the stock solution on ice.
»O2k manual titrations: MiPNet09.12
  • Titration volume (2-mL O2k-chamber): 1-3 µL using a 10 µL Hamilton syringe.
  • 3 µL of H2O2 into the 2-mL O2k-chamber increases the concentration of O2 by approx. 150 nmol/mL (150 µM).


Preparation of 50 mM stock solution (dissolved in H2O) for 0.5-mL O2k-chamber:
  1. Pipette 28 µL of 17.6 M H2O2 into 10 mL plastic vial.
  2. Add H2O, acidify with HCl (1 mM) to pH 6, complete with H2O to a total volume of 10 mL. Maintain the pH in the stock solution acidic to minimize autoxidation.
  3. Wrap plastic vial in aluminum foil (solution is light-sensitive) and store at 4 °C.
  4. During experiments keep the stock solution on ice.
»O2k manual titrations: MiPNet09.12
  • Titration volume (0.5-mL O2k-chamber): 1-3 µL using a 10 µL Hamilton syringe.
  • 3 µL of H2O2 into the 2-mL O2k-chamber increases the concentration of O2 by approx. 150 nmol/mL (150 µM).


Limitations of using MiR media

  • MiR06 or MiR06Cr cannot be used for measurement of ROS production. Use MiR05 or MiR05Cr instead.
  • The high antioxidant activity may compete with reactions on which measurement of ROS production is based.
  • The intracellular milieu of kidney has a low [K+]. Kidney mitochondria are inhibited by the high [K+] of MiR05 to MiR06Cr [1].

>> MiPMap - Is this a general issue for the organ, or is it in addition also a species issue?

  1. A mitochondrial respiration medium for kidney: Friederich-Persson 2012 Diabetologia.

Further information

  • MiPNet08.05 and MiPNet10.11 are integrated in MiPNet14.13_Medium-MiR06.

Original publication introducing MiR05: