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Difference between revisions of "Dithionite"

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{{MitoPedia
{{MitoPedia
|abbr=Dith
|abbr=Dith
|description=Zero oxygen solution powder, Na<sub>2</sub>S<sub>2</sub>O<sub>4</sub>, used for [[MiPNet19.18D O2k-Series G and DatLab 6: Calibration |calibration of oxygen sensors]] at zero oxygen, or for stepwise reduction of oxygen concentration in [[MiPNet14.06 Instrumental O2 background |instrumental O<sub>2</sub> background tests]].
|description='''Dithionite''' Na<sub>2</sub>S<sub>2</sub>O<sub>4</sub> is the 'zero oxygen solution powder' used for [[Oxygen calibration - DatLab |calibration of oxygen sensors]] at zero oxygen, or for stepwise reduction of oxygen [[concentration]] in [[MiPNet14.06 Instrumental O2 background |instrumental O<sub>2</sub> background tests]]. It is not recommended to use dithionite in experiments with biological samples or several multisensor approaches.
|info=[[MiPNet06.03 POS-calibration-SOP]], [[MiPNet14.06 Instrumental O2 background]]
|info=[[MiPNet06.03 POS-calibration-SOP]], [[MiPNet14.06 Instrumental O2 background]]
}}
}}
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{{MitoPedia methods
|mitopedia method=Respirometry
}}
{{MitoPedia O2k and high-resolution respirometry}}
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{{Template:OSC Oxygen signal1}}
{{Template:OSC Oxygen signal1}}
{{MitoPedia methods
|mitopedia method=Respirometry
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{{MitoPedia O2k and high-resolution respirometry
|mitopedia O2k and high-resolution respirometry=O2k-Open Support
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{{MitoPedia topics
|mitopedia topic=Substrate and metabolite
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Revision as of 10:21, 29 May 2020


high-resolution terminology - matching measurements at high-resolution


Dithionite

Description

Dithionite Na2S2O4 is the 'zero oxygen solution powder' used for calibration of oxygen sensors at zero oxygen, or for stepwise reduction of oxygen concentration in instrumental O2 background tests. It is not recommended to use dithionite in experiments with biological samples or several multisensor approaches.

Abbreviation: Dith

Reference: MiPNet06.03 POS-calibration-SOP, MiPNet14.06 Instrumental O2 background


Template NextGen-O2k.jpg


MitoPedia O2k and high-resolution respirometry: O2k-Open Support 



Preparation

Preparation of 30 mM dithionite solution for instrumental oxygen background test (dissolved in Phosphate buffer, 50 mM, pH 8)
  1. Weigh 0.051 g dithionite, sodium hydrosulfite, and transfer to 10 mL volumetric glass flask.
  2. Adjust final volume to 10 mL with Phosphate buffer and keep closed to avoid decomposing.
Preparation of 10 mM dithionite solution for instrumental oxygen background test (dissolved in Phosphate buffer, 50 mM, pH 8)
  1. Weigh 0.017 g dithionite, sodium hydrosulfite, and transfer to 10 mL volumetric glass flask.
  2. Adjust final volume to 10 mL with Phosphate buffer and keep closed to avoid decomposing.
Note: Experiments performed with 10 and 30 mM dithionite solution showed identical results. Sodium dithionite is oxidized when exposed to air. We recommend to reduce contact to air during preparation and usage (closed tube). We advise to use a concentration of 30 mM for performing the instrumental oxygen background test. For new dithionite, 10 mM dithionite solution may be used.
Preparation of 2.5 mM dithionite solution for instrumental oxygen background test with the O2k-sV-Module (0.5 mL) (dissolved in Phosphate buffer, 50 mM, pH 8)
  1. Weigh 0.00425 g dithionite, sodium hydrosulfite, and transfer to 10 mL volumetric glass flask.
  2. Adjust final volume to 10 mL with Phosphate buffer and keep closed to avoid decomposing.
Note: Experiments performed with 2.5 mM dithionite solution are recommended for the O2k-sV-Module only. Sodium dithionite is oxidized when exposed to air. We recommend to reduce contact to air during preparation and usage (closed tube).


Further information »Talk:Dithionite

Troubleshooting

Zero oxygen concentration reached but 'Instrumental O2 background_TIP2k.DLP' is not finished

Question:

We have always had the same issue with our TIP2k running the background calibration that it has always reached ‘TIP2 end’ with the oxygen concentration reaching zero before the event P004 was activated meaning we are not able to get mark J°4h. The data is attached (2019-11-04).

2019-11-04 P2-01 Instrumental Background.PNG

Answer:

Stepwise analysis of the attached data shows the following:

Observations:

Default parameters high O2 background TIP2K (.DLD)
Volume (nL) Flow (nL/s)
P1 100000 250
P2 100000 250
P3 50000 125
P4 100000 50000
Your high O2 background TIP2K (.DLD)
P1 100000 250
P2 50000 125
P3 100000 50000
P4 x x

Please note that: On your protocol the event P2 has been missed (if you see, the default P3 and your P2 are the same steps); A premise for P1 (please see on your DLD file under 'Feedback control' and after loading as protocol 'BG_Feedback-highO2_400-200') is to start when O2 concentration [µM] > 370 and to stop when O2 concentration [µM] < 360.

However: immediately after your P1 titration, you already have a O2 concentration [µM] = 322 and therefore your titration P1 goes on until the requirements for the next possible P titration are met; The next possible titration requirements corresponds to P3 (in your DLD recognized as P2) (start when O2 concentration [µM] > 270 and to stop when O2 concentration [µM] < 260); Finally the P4 titration takes place (in your DLD recognized as P3) which corresponds to a 100 uL titration just before the event 'TIP end'.

Conclusion: Since we observe that your O2 concentration decreases too fast at each Dith titration point, we can be sure that the Dith solution stock has an high concentration. Our recommendation for Dith concentration is between 10 and 30 mM. Due to the oxidation process that occurs when Dith is open for long time, we recommend to use a concentration of 30 mM for performing the instrumental oxygen background test, however in your case I advise you to use a lower concentration of your Dith solution.

During instrumental oxygen background test, the step representative of O2 consumption is too small after Dith titrations

  • Customer ID: CH Lausanne Kayser B

Question:

I ran a zero oxygen calibration after the instrumental background protocol and the O2 neg slope for O2 concentrations of 60 and 30 uM is positive and greater compared with the O2 neg slope at O2 concentrations of 180 and 120 uM. The data is attached (2019-09-11).

Dith oxidized 2019-09-11 P1-05.DLD.png

Answer: Stepwise analysis of the attached data shows the following:

Quality control (QC) 1: Your POS operates perfectly: during air calibration the O2 slope neg. approaches zero (see section 2.1 of https://wiki.oroboros.at/images/7/77/MiPNet06.03_POS-Calibration-SOP.pdf);

Quality control (QC) 2: In the closed chamber, the O2 slope neg. is <4 pmol s-1 mL-1 which excludes any biological or chemical contamination from the MiR05 buffer. https://wiki.oroboros.at/images/6/65/MiPNet14.06_InstrumentalO2Background.pdf;

  • From your dithionite titrations we can observed that:
  1. After titrations of 2.5 µL of Dith, the step representative of O2 consumption is too small – indicative of a low effective potency of the solution of Dith;
  2. At increasing concentrations of Dith towards stepwise lower O2 concentrations, we observe that the O2 slope negative does not decrease in a titration dependent manner. Therefore, O2 is being consumed by the solution even after the initial fast decline of oxygen. Since we excluded other potential problems, the irregular background traces are due to the Dith solution.(see representative trace on page 5 of https://wiki.oroboros.at/images/6/65/MiPNet14.06_InstrumentalO2Background.pdf)

Taken together, your dithionite is highly oxidised and a continuing oxidation reaction explains the results.

Solution: Assuming you prepared the Dith according to our SOP (always fresh, http://bioblast.at/index.php/Dithionite), I advise you to purchase a new Dith powder (your Dith may be old and/or has oxidized).

Anonymous user

Question:

Q1: The Oxygen Concentration couldn't go down while I tried zero oxygen calibration. No matter how much solution I added, the oxygen concentration still remain the same. I reassembled, but it still keeps the same. The data is attached.

No response to dithionite.PNG


Q2: The chamber B's oxygen slope is not stable. This is a new problem I have never seen. Please see the attachment.(2019-04-26)

Signal stability.PNG


Q3. The maximum Oxygen concentration of another Oroboros O2k is only about 140 μM. I don't how to increase the starting point of oxygen concentration.


Answer:

A1: I suspect that the dithionite solution was not correctly prepared or not fresh. Dithionite loses activity quite fast, so you need to make it freshly. Please check this site: http://bioblast.at/index.php/Dithionite

A2: While there is a difference between chambers A and B, the stability of the signal is still within the acceptable range of noise given by the specifications of the instrument, see: Oxygen_sensor_test.

A3: You may simply need to calibrate, please see here: http://wiki.oroboros.at/index.php/O2_calibration_-_DatLab


MitoPedia methods: Respirometry 


MitoPedia O2k and high-resolution respirometry: O2k-Open Support 


MitoPedia topics: Substrate and metabolite