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TermDescription
Fischer 2021 MitoFit Fe liver
Fischer 2022 MitoFit Fe
Fluo calibration - DatLab
Fluorescence-Control Unit
Fluorescence-Control Unit lettered.jpg

Fluorescence-Control Unit with O2k-Front Fixation, Current-Control (O2k-Chamber A and B) for regulation of light intensity of the LED in the fluorescence sensors. This item is a standard component of the O2k-Fluorescence LED2-Module.

Fluorescence-Sensor Blue
Fluorescence-Sensor Green.JPG

Fluorescence-Sensor Blue: excitation LED 465 nm (dominant wavelength), photodiode, Filter-Cap equipped with Filter Set Saf for measurement of mitochondrial membrane potential with Safranin when delivered. The filter set Filter Set MgG / CaG for Magnesium green庐 / Calcium green庐 measurements is included.

Fluorescence-Sensor Green
Fluorescence-Sensor Green.JPG

Fluorescence-Sensor Green: excitation LED 525 nm (dominant wavelength), photodiode, Filter-Cap equipped with Filter Set AmR for Amplex UltraRed measurements when delivered.

Flux / SlopeFlux / Slope is the time derivative of the signal. In DatLab, Flux / Slope is the name of the pull-down menu for (1) normalization of flux (chamber volume-specific flux, sample-specific flux or flow, or flux control ratios), (2) flux baseline correction, (3) Instrumental background oxygen flux, and (4) flux smoothing, selection of the scaling factor, and stoichiometric normalization using a stoichiometric coefficient. Before changing the normalization of flux from volume-specific flux to sample-specific flux or flow, or flux control ratios, please be sure to use the standard Layout 04a (Flux per volume) or 04b (Flux per volume overlay). When starting with the instrumental standard Layouts 1-3, which display the O2 slope negative, the sample-specific flux or flow, or flux control ratios will not be automatically background corrected. To obtain the background corrected specific flux or flux control ratios, it is needed to tick the background correction in the lower part of the slope configuration window. Background correction is especially critical when performing measurements in a high oxygen regime or using samples with a low respiratory flux or flow.
Flux analysis - DatLabThe strategy of Flux analysis using DatLab depends on the research question and the corresponding settings applied in DatLab when recording the data with the O2k. Usng SUIT protocols, a sequence of respiratory steady-states is measured, marks are set, and numerical data are summarized in Mark statistics (F2). An AI approach is kept in mind when describing guidelines for evaluation of steady-states during data recording and analysis.
Flux baseline correction

Flux baseline correction provides the option to display the plot and all values of the flux (or flow, or flux control ratio) as the total flux, J, minus a baseline flux, J0.

JV(bc) = JV - JV0
JV = (dc/dt) 路 -1SF - J掳V

For the oxygen channel, JV is O2 flux per volume [pmol/(s路ml)] (or volume-specific O2 flux), c is the oxygen concentration [nmol/ml = 碌mol/l = 碌M], dc/dt is the (positive) slope of oxygen concentration over time [nmol/(s 路 ml)], -1 = -1 is the stoichiometric coefficient for the reaction of oxygen consumption (oxygen is removed in the chemical reaction, thus the stoichiometric coefficient is negative, expressing oxygen flux as the negative slope), SF=1,000 is the scaling factor (converting units for the amount of oxygen from nmol to pmol), and J掳V is the volume-specific background oxygen flux (Instrumental background oxygen flux). Further details: Flux / Slope.

Flux control ratio

Flux control ratios FCRs are ratios of oxygen flux in different respiratory control states, normalized for maximum flux in a common reference state, to obtain theoretical lower and upper limits of 0.0 and 1.0 (0 % and 100 %).

For a given protocol or set of respiratory protocols, flux control ratios provide a fingerprint of coupling and substrate control independent of (1) mt-content in cells or tissues, (2) purification in preparations of isolated mitochondria, and (3) assay conditions for determination of tissue mass or mt-markers external to a respiratory protocol (CS, protein, stereology, etc.). FCR obtained from a single respirometric incubation with sequential titrations (sequential protocol; SUIT protocol) provide an internal normalization, expressing respiratory control independent of mitochondrial content and thus independent of a marker for mitochondrial amount. FCR obtained from separate (parallel) protocols depend on equal distribution of subsamples obtained from a homogenous mt-preparation or determination of a common mitochondrial marker.

Forceps for membrane application
Forcep for membrane application.jpg

Forceps for membrane application: for OroboPOS and ISE membrane application; do not use for tissue preparation.

Forceps\stainless Steel\angular Tip\fine
Forcep for tissue preparation angular tip.jpg

Forceps\stainless Steel\angular Tip\fine: for tissue preparation, stainless steel. Two pairs are used particularly for muscle fiber separation.

Forceps\stainless Steel\rounded Tip\sharp
Forcep for tissue preparation rounded tip.jpg

Forceps\stainless Steel\rounded Tip\sharp: for tissue preparation, stainless steel, antimagnetic. One pair is recommended for placing the tissue sample onto the microbalance and for handling in combination with Forceps\stainless Steel\straight Tip\sharp.

Forceps\stainless Steel\straight Tip\sharp
Forcep for tissue preparation straight tip.jpg

Forceps\stainless Steel\straight Tip\sharp: for tissue preparation, stainless steel, antimagnetic. One pair is recommended for insertion of the sample into the O2k-chamber and for handling in combination with Forceps\stainless Steel\rounded Tip\sharp.

Fraser 2018 Nature
Full screenBy clicking/enabling Full screen in the Graph-menu in DatLab the currently selected graph is shown alone on the full screen (On) or together with the other defined graphs (Off). Full screen is particularly useful for a single channel overview and for Copy to clipboard [ALT+G B].
Functional Mitochondrial Diagnostics
GDPR
GRC Meeting on Organelles including Mitochondria 2019 West Dover US
GRC Mitochondria in Health and Disease 2023 Lucca IT
GRC on Mitochondrial Dynamics and Signaling 2019 Ventura US
GRS on Mitochondria & Chloroplasts 2022 West Dover US
GainThe gain is an amplification factor applied to an input signal to increase the output signal.
Ganguly 2022 MitoFit
Garcia-Roves Pablo Miguel
Getting started - DatLabUsers have to enter their user details the first time they use DatLab 8 on a specific computer. As well, entering some basic settings is required when connecting DatLab 8 with an O2k for the first time.
Ginsparg 2017 arXiv
Gnaiger 2012 Mitochondr Physiol Network Bioblast 2012
Gnaiger 2014 MitoPathways
Gnaiger 2019 MitoFit Preprints
Gnaiger 2019 MitoFit Preprints Editorial
Gnaiger 2020 BEC MitoPathways
Gnaiger 2020 MitoFit x
Gnaiger 2021 MitoFit BCA
Gnaiger Erich
Gnaiger IOC62-Introduction
Gon莽alves 2019 Mitofit Preprint Arch EA
Gradl P
Graph control - DatLabA combination of mouse and keyboard commands provides convenient control of graphs in DatLab 8.
Graph layout - DatLabSee Layout for DatLab graphs.
Graph options - DatLabSeveral display options can be applied to a DatLab graph under Graph options.
Greenland Expedition CMRC 2004
Gross 2018 Neurology
Gurkina A
HR Split Ljubkovic M
HU Budapest Chinopoulos C
HU Budapest Semmelweis Univ
HU Budapest Tretter L
HU Debrecen Virag L
HU Szeged Boros M
Haider Markus
Hassan 2020 MitoFit Preprint Arch
Hatch 1998 JAMA
Heichler 2022 MitoFit
Heimler 2022 MitoFit
High signal at zero oxygenA high signal at zero oxygen may be observed during zero calibration (R0). First, check the quality of the dithionite solution. The following instructions show how to distinguish between a defective sensor head and an electrical leak current.
Holzner 2019 MitoFit Preprint Arch EA
Houska Award 2012
Huete-Ortega 2020 MitoFit Preprint Arch EA
Huete-Ortega Maria
Hydrogen peroxide
Hydrogen peroxide

Hydrogen peroxide, H2O2 or dihydrogen dioxide, is one of several reactive oxygen intermediates generally referred to as reactive oxygen species (ROS). It is formed in various enzyme-catalyzed reactions (e.g., superoxide dismutase) with the potential to damage cellular molecules and structures. H2O2 is dismutated by catalase to water and oxygen. H2O2 is produced as a signaling molecule in aerobic metabolism and passes membranes more easily compared to other ROS.

Hydrogenion flux

Volume-specific hydrogenion flux or H+ flux is measured in a closed system as the time derivative of H+ concentration, expressed in units [pmol路s-1路mL-1]. H+ flux can be measured in an open system at steady state, when any acidification of the medium is compensated by external supply of an equivalent amount of base. The extracellular acidification rate (ECAR) is the change of pH in the incubation medium over time, which is zero at steady state. Volume-specific H+ flux is comparable to volume-specific oxygen flux [pmol路s-1路mL-1], which is the (negative) time derivative of oxygen concentration measured in a closed system, corrected for instrumental and chemical background.

pH is the negative logarithm of hydrogen ion activity. Therefore, ECAR is of interest in relation to acidification issues in the incubation buffer or culture medium. The physiologically relevant metabolic H+ flux, however, must not be confused with ECAR.

IE Dublin Miinalainen I
IE Dublin O Gorman D
IE Dublin Porter RK
IL Ramat Gan Yardeni T
IL Rishon Le Zion Hachmo Y
IN Chennai Labmate
IN Haldia Chakrabarti S
IN Hyderabad Thangaraj K
IN Lucknow Gayen JR
IN Mumbai Kolthur-Seetharam U
IN New Delhi Mukhopadhyay A
IN Thiruvananthapuram Gopala S
IN Varanasi Dash D
IOC Innsbruck
IOC Schroecken
IOC recommended reading
IOC student scholarship
IOC05
IOC10
IOC13
IOC16
IOC33
IOC42
IOC43 Montevideo UY 2007
IOC48
IOC62
IPC2021 Puerto Varas CL
ISAP 2021 Virtual
ISE Package 1 TPP or Ca
ISE Package 1 TPP or Ca.JPG

O2k-TPP+ and Ca2+ ISE\1 Chamber: ISE-Package for 1 TPP+ and Ca2+ electrode.

ISE-Ca2+ Membranes
Ca2+ membranes.jpg

ISE-Ca2+ Membranes: PVC, 4 mm diameter, box of 5 membranes.

To be used with the O2k-TPP+ ISE-Module.

ISE-Compressible Tube
ISE-Compressible Tube.JPG

ISE-Compressible Tube for Ion-Selective Electrode TPP+ and Ca2+.

ISE-Filling Syringe
ISE-Filling Syringe.JPG

ISE-Filling Syringe with needle for Ion-Selective Electrode TPP+ and Ca2+.

ISE-Inner Glass Electrode
ISE-Inner Glass Electrode.JPG

ISE-Inner Glass Electrode of ISE, with Ag/AgCl- and Pt-wire

ISE-Membrane Mounting Tool
ISA-Membrane Mounting Tool.JPG

ISE-Membrane Mounting Tool for Ion-Selective Electrode TPP+ and Ca2+.

O2k-TPP+ ISE-Module: mounting tool included.

ISE-Membrane Seal
ISE-Membrane Seal.JPG

ISE-Membrane Seal for Ion-Selective Electrode TPP+ and Ca2+.

ISE-TPP+ Membranes
ISE-TPP+ Membranes.JPG

ISE-TPP+ Membranes, PVC, 4 mm diameter, box of 5 membranes.

ISS-Filter and Tubing
ISS-Filter and Tubing.JPG

ISS-Filter and Tubing, ISS-Integrated Suction System.

ISS-Integrated Suction System
ISS.jpg

ISS-Integrated Suction System: Suction pump with stainless steel housing, 2 liter waste bottle, filter and tubing; for siphoning off excess medium from the O2k-Stopper and for emptying the O2k-chambers. The ISS is included as a standard component of the O2k-FluoRespirometer. Media containing living cells or microorganisms, various poisons (inhibitors, uncouplers) and mixtures of proteins and substrates are safely disposed off in the 2-litre waste bottle.

ISS-Lid
ISS-Lid.JPG

ISS-Lid, for ISS-Waste Bottle, component of the ISS-Integrated Suction System.

ISS-Steel Housing
ISS-Steel Housing.JPG

ISS-Steel Housing, a component of the ISS-Integrated Suction System.

ISS-Waste Bottle
ISS-Waste Bottle.JPG

ISS-Waste Bottle, 2-liter, component of the ISS-Integrated Suction System.

IT Bari Atlante A
IT Bari Cantatore P
IT Bari Palmieri L
IT Bologna Genova ML
IT Bolzano Pichler I
IT Cagliari Lai N
IT Catania Messina A
IT Florence Morandi A
IT Foggia Capitanio N
IT Milan Clementi E
IT Naples Iossa S
IT Novara Filigheddu N
IT Padova Morosinotto T
IT Padova Viscomi C
IT Pozzuoli Ligresti A
IT Rome Giuffre A
IT Rome Scatena R
IT Udine Grassi B
IT Udine Mavelli I
IT Verona Calabria E
IT Verona Venturelli M
Iglesias-Gonzalez Javier
IlluminationThe chambers of the Oroboros O2k are illuminated by an internal LED. The illumination is switched on and off in DatLab during the experiment by pressing [F10]. This illumination must be distinguished from light introduced into the chambers by LEDs for the purpose of spectrophotometric and fluorometric measurements. For these, the internal illumination must be switched off.
Illumination on/offThe illumination in both chambers is switched on/off.
Ingram 2020 MitoFit Preprint Arch
Innovationsscheck PLUS
Innovationsscheck PLUS 2
Install Oroboros protocol packageThe standard Instrumental and SUIT DL-Protocols package is automatically implemented with the simple DatLab programme installation. We recommend a 'clean install': rename your previous DatLab programme subdirectory (e.g. C:\DatLab_OLD). Updates and newly developed DL protocols can be simply downloaded by clicking on [Protocols]\Install Oroboros protocol package.
Installation and startup support session self-study material
Instrumental: Browse DL-Protocols and templatesInstrumental DL-Protocols (DLP) including DatLab example traces, instructions, brief explanatory texts, links to relevant pages and templates for data evaluation can be browsed from inside DatLab 7.4. Click on menu [Protocols]\Instrumental: Browse DL-Protocols and templates to open a folder with all the DL-Protocols and templates for cleaning, calibration, and background determination provided with the DatLab 7.4. Select a sub-directory and open an DL-Protocol and/or template as desired.
Interpolate pointsSelect Interpolate points in the Mark information window to interpolate all data points in the marked section of the active graph. See also Delete points and Restore points or Recalculate slope.
Ion-Selective Electrode TPP+ and Ca2+
Ion-Selective Electrode TPP+ and Ca2+.JPG

Ion-Selective Electrode TPP+ and Ca2+: ISE with 6 mm outer diameter shaft, for Stopper\white PVDF\angular Shaft\side+6.2+2.6 mm Port.

O2k-TPP+ ISE-Module: 2 ISE.

Iwema 2016 F1000Research
JP Ibaraki Nakayama T
JP Sagamihara Kobayashi H
JP Sapporo Yokota T
JP Tokushima Okuno H
JP Tokyo Berthold
JP Tokyo Sanyo
JP Tokyo Tanaka M
JP Tokyo Uchino H
Jackson 2002 Notices Amer Mathemat Soc
Jacobs Howard T
Jusic 2019 MitoFit Preprint Arch EA
K-Regio MitoCom Tyrol (de)
K-Regio MitoFit
KR Busan Han J
KR Incheon Kwak HB
KR Seongnam Lee J
KR Seoul Lee HK
KR Seoul Mymed
KR Seoul Pak YK
KR Seoul Scitech Korea
KR Ulsan Lim CH
Kaiser 2017 Science
Kaiser 2017 Science 357
Karabatsiakis Alexander
Karavyraki 2022 MitoFit
Keyboard shortcuts - DatLabDatLab provides several keyboard shortcuts to allow for quick access to many functions and settings without using a mouse.
King B
Klein 2018 Int J Digit Libr
Kleinert 2018 Lancet
Komlodi 2021 MitoFit AmR-O2
Komlodi 2021 MitoFit Q
Komlodi Timea
Krako Jakovljevic 2021 MitoFit PD
LT Kaunas Baniene R
LT Kaunas Borutaite V
LT Kaunas Briedis V
LT Vilnius Zimkus A
LV Riga Jansone B
LV Riga Liepins E
Laboratory titration sheetLaboratory titration sheet contains the sequential titrations in a specific Substrate-uncoupler-inhibitor titration (SUIT) protocol. The laboratory titration sheets for different SUIT protocols are incorporated in DatLab (DL7.1): Protocols in DatLab
Laner Verena
Layout for DatLab graphsA Layout in DatLab selected in the Layout menu yields a standardized display of graphs and plots displayed with specific scalings. The graph layout defines initial settings, which can be modified for plots [Ctrl+F6] and scaling [F6]. A modified layout can be saved as user layout without changing the standard layouts.
Learn 2019 Nature
Life Science PhD Meeting 2019 Innsbruck AT
Life Sciences Meeting 2018 Innsbruck AT
Light-enhanced dark respirationLight-enhanced dark respiration LEDR is a sharp (negative) maximum of dark respiration in plants in response to illumination, measured immediately after switching off the light. LEDR is supported by respiratory substrates produced during photosynthesis and closely reflects light-enhanced photorespiration (Xue et al 1996). Based on this assumption, the total photosynthetic oxygen flux TP is calculated as the sum of the measured net photosynthetic oxygen flux NP plus the absolute value of LEDR.
Long Night of Research 2018 Innsbruck AT
Long Night of Research 2020 Virtual Event
Long Night of Research 2022 Innsbruck AT
Long Night of Research 2024 Innsbruck AT
Lower O2 limit - DatLabA Lower O2 limit [碌M] can be defined for each O2k-chamber, to trigger an automatic warning when the experimental O2 concentration drops below this limit. It reminds the user that re-oxygenation of the O2k-chamber may be required. For the lower O2 concentration limit, the critical oxygen concentration should be considered, which differs between isolated mitochondria, large cells, and permeabilized muscle fibers. A higher limit should be chosen when high oxygen flux is expected, e.g. prior to uncoupler titration. A lower limit is acceptable prior to inhibition of respiration causing low oxygen flux.
MBSJ 2018 Yokohama JP
MITOEST 2018 Tallinn EE
MX Mexico City Aguirre J
MX Mexico City Pedraza Chaverri J
MX Mexico City Uribe-Carvajal S
MX Mexiko City Moreno-Sanchez R
MX San Pedro Garcia-Rivas G
MY Kuala Lumpur Abdul Karim N
Machado 2019 MitoFit Preprint Arch EA
Maggio 2018 Perspect Med Educ
Magnesium GreenMagnesium Green (MgG) is an extrinsic fluorophore that fluoresces when bound to Mg2+ and is used for measuring mitochondrial ATP production by mitochondrial preparations. Determination of mitochondrial ATP production is based on the different dissociation constants of Mg2+ for ADP and ATP, and the exchange of one ATP for one ADP across the mitochondrial inner membrane by the adenine nucleotide translocase (ANT). Using the dissociation constants for ADP-Mg2+ and ATP-Mg2+ and initial concentrations of ADP, ATP and Mg2+, the change in ATP concentration in the medium is calculated, which reflects mitochondrial ATP production.
Manage setups and templates - DatLabSetups and templates in DatLab can be renamed or deleted under Manage setups or Manage templates.
Manuscript template for MitoFit PreprintsManuscripts template for MitoFit Preprints and Bioenergetics Communications.
Mark information禄 See Marks - DatLab
Mark specifications - DatLabThe function Mark specifications is largely replaced by SUIT DL-Protocols and Instrumental DL-Protocols in DatLab 7.4. Mark specifications allow the user to rename Marks in the active plot and save/recall the settings. Rename marks individually by clicking into the horizontal bar, or use corresponding templates for renaming the entire sequence of marks.
Mark statistics - DatLabIn Mark statistics one Plot is selected as a source for Marks over sections of time. Values (e.g. medians) are displayed for these time sections of the source plot and of all selected plots.
Marks - DatLabMarks in DatLab define sections of a plot recorded over time. Marks are set by the user in real-time, or post-experimentally for basic level data analysis. Set Marks to obtain the median, average, standard deviation, outlier index and range of the data within the mark, for calibration of the oxygen signal, flux analysis, or to delete marked data points. Marks are shown by a horizontal bar in the active plot. The default Mark names are given automatically in numerical sequence, independent for each plot. Rename marks individually by clicking into the horizontal bar, or use corresponding templates for renaming the entire sequence of marks.Several marks can be set on any plot, but marks cannot overlap within a plot and are separated by one or more data points which are not marked.
MiP2019/MitoEAGLE Belgrade RS
MiPMap
MiPMap

The project Mitochondrial Physiology Map (MiPMap) is initiated to provide an overview of mitochondrial properties in cell types, tissues and species. As part of Bioblast, MiPMap may be considered as an information synthase for Comparative Mitochondrial Physiology. Establishing a comprehensive database will require global input and cooperation.

A comparative database of mitochondrial physiology may provide the key for understanding the functional implications of mitochondrial diversity from mouse to man, and evaluation of altered mitochondrial respiratory control patterns in health and disease (Gnaiger 2009).

MiPNet
MiPNet 26.15 NextGen-O2k Event Photobiology: Algal bioenergetics Innsbruck AT
MiPNet 26.16 NextGen-O2k Summit 2021 Virtual
MiPNet Events
MiPNet02.03 DatLab2 Flux analysis
MiPNet02.04 DatLab2 TimeConstant
MiPNet02.05 DatLab2 O2Kinetics
MiPNet02.06 DatLab2
MiPNet02.07 Datlab2 Manual
MiPNet03.01 Diagnosis
MiPNet03.02 Chemicals-Media
MiPNet03.03 Internat-Oxygraph-Workshops
MiPNet04.02 DatLab 2.1
MiPNet04.03
MiPNet04.04
MiPNet04.06 IOC18
MiPNet05.01
MiPNet05.02
MiPNet05.03
MiPNet06.01 O2k-Overview
MiPNet06.03 POS-calibration-SOP
MiPNet06.05 Test Experiments on O2k-Specifications
MiPNet06.06 Chemical O2 background
MiPNet06.07
MiPNet06.08 Weinatmung
MiPNet06.09 IOC19
MiPNet07.02 IOC20
MiPNet07.03
MiPNet07.04 Oxygraph-2kP2
MiPNet07.05 IOC21
MiPNet07.06 Oxygraph-2k
MiPNet07.07 O2k-NetworkInvitation
MiPNet07.08 User information
MiPNet08.02 IOC23
MiPNet08.03
MiPNet08.11 IOC24
MiPNet08.12 IOC22
MiPNet08.13 mt-Isolation-RLM
MiPNet08.15 Complex-I
MiPNet08.16 pH calibration
MiPNet08.17 IOC26
MiPNet09.01 O2k-ParadigmShift
MiPNet09.02 IOC27
MiPNet09.03
MiPNet09.05 IOC28
MiPNet09.11 IOC29
MiPNet09.12 O2k-Titrations
MiPNet10.02 IOC30
MiPNet10.03
MiPNet10.04 CellRespiration
MiPNet10.08 IOC31
MiPNet10.10 O2k-Folder
MiPNet11.01
MiPNet11.02 IOC32
MiPNet11.03 IOC35 Schroecken
MiPNet11.04 MitoPathways-CI
MiPNet11.05 imt-pti-pce
MiPNet11.06 IOC36
MiPNet11.07
MiPNet11.08
MiPNet11.09 MitoPathways-CII
MiPNet12.01 Suppl T-issue
MiPNet12.02 DatLab4.2 NewFeatures
MiPNet12.03 IOC37
MiPNet12.04 IOC38
MiPNet12.05
MiPNet12.10 TIP2k-manual
MiPNet12.11 MitoRespiration
MiPNet12.13 Q-JunctionSCR
MiPNet12.14 IOC39
MiPNet12.15 RespiratoryStates
MiPNet12.17 BovineHeartMito
MiPNet12.19 IOC41
MiPNet12.20 O2k-calibration tutorial
MiPNet12.22
MiPNet12.23 FiberRespiration
MiPNet12.24 IOC44
MiPNet13.01
MiPNet13.02 IOC46
MiPNet13.03 MiPArt-03
MiPNet13.04 IOC47
MiPNet13.06 MiPArt-04
MiPNet14.01 ESD-damage
MiPNet14.02 IOC49
MiPNet14.03 IOC50
MiPNet14.04 IOC51
MiPNet14.05 TPP-mtMembranePotential
MiPNet14.06 Instrumental O2 background
MiPNet14.07 MiPArt-05
MiPNet14.08 IOC52
MiPNet14.11 IOC53
MiPNet14.13 Medium-MiR06
MiPNet14.14 PermeabilizedFiberPreparation
MiPNet14.15 IOC54
MiPNet15.01 IOC55
MiPNet15.02 IOC56
MiPNet15.03 O2k-MultiSensor-ISE
MiPNet15.05 NO-manual
MiPNet15.07 IOC59
MiPNet15.08 TPP electrode
MiPNet15.09. Yeast: HRR Reference Assay
MiPNet15.10 IOC60
MiPNet15.10 IOC60 Abstracts
MiPNet15.11 IOC58
MiPNet15.12 IOC57 Druskininkai LT
MiPNet16.01 IOC61
MiPNet16.01 IOC61 Abstracts
MiPNet16.02 IOC64
MiPNet16.03 IOC65
MiPNet16.04 IOC62
MiPNet16.05 IOC63
MiPNet17.02 PBI-Shredder manual
MiPNet17.03 Shredder vs Fibers
MiPNet17.04 CitrateSynthase
MiPNet17.05 O2k-Fluo LED2-Module
MiPNet17.06 IOC66
MiPNet17.07 IOC67
MiPNet17.08 IOC68 Schroecken AT
MiPNet17.09 IOC Questions
MiPNet17.10 IOC70
MiPNet17.12 Bioblast 2012
MiPNet17.14 IOC72 Schroecken AT
MiPNet17.15 PBI-Shredder Mouse-heart-brain-liver
MiPNet17.16 O2k-Spectrophotometry
MiPNet17.17 Amplex-Mouse-brain
MiPNet17.18 MitoPathways
MiPNet17.19 IOC69
MiPNet17.20 IOC71
MiPNet18.01 IOC73
MiPNet18.02 IOC74
MiPNet18.03 IOC75 Abstracts
MiPNet18.03 IOC75 Schroecken AT
MiPNet18.04 IOC76
MiPNet18.05 Amplex-Mouse-heart
MiPNet18.06 Amplex-Yeast
MiPNet18.07 IOC79
MiPNet18.09 IOC80 Schroecken AT
MiPNet18.10 O2k-Specifications
MiPNet18.11 IOC82
MiPNet18.13 IOC84 Alaska
MiPNet18.14 IOC85
MiPNet18.15 IOC86
MiPNet18.16 IOC87 Spitsbergen
MiPNet18.17 IOC83
MiPNet18.18 IOC77
MiPNet18.19 IOC81
MiPNet18.20 IOC78
MiPNet19.01 O2k-Core Manual Series F DatLab 5
MiPNet19.01A O2k-Start
MiPNet19.01C DatLab Guide
MiPNet19.01E O2 Flux Analysis
MiPNet19.02 IOC88 Schroecken AT
MiPNet19.03 O2k-cleaning and ISS
MiPNet19.04 IOC89 La Jolla US
MiPNet19.05 IOC90 Bolzano IT
MiPNet19.06 IOC91 Philadelphia US
MiPNet19.07 IOC92
MiPNet19.08 IOC93
MiPNet19.09 IOC94 Shanghai CN
MiPNet19.10 IOC95 Obergurgl
MiPNet19.11 IOC96 Schroecken AT
MiPNet19.14 SOP Hamilton microsyringes
MiPNet19.15 IOC97
MiPNet19.16 IOC98
MiPNet19.17 O2k Series G
MiPNet19.18 O2k-Series G Core manual
MiPNet19.18A O2k-Series G: Start
MiPNet19.18B POS-service
MiPNet19.18C DatLab 6: Guide
MiPNet19.18D O2k-Series G and DatLab 6: Calibration
MiPNet19.18E O2 flux analysis - DatLab 6
MiPNet19.19 DatLab 6
MiPNet19.20 Cytochrome c control efficiency
MiPNet20.01 IOC100 Schroecken
MiPNet20.02 IOC99 Cape Town
MiPNet20.03 IOC101 London
MiPNet20.04 O2k-checklist
MiPNet20.05 IOC104 Greenville
MiPNet20.06 IsolationMouseHeart-mt
MiPNet20.07 IsolationRatBrain-mt
MiPNet20.08 IsolationRatLiver-mt
MiPNet20.09 IsolationBeefHeart-mt
MiPNet20.10 IOC106 Schroecken
MiPNet20.11 IOC102 Wuhan CN
MiPNet20.12 IOC103 Manaus
MiPNet20.13 Safranin mt-membranepotential
MiPNet20.14 AmplexRed H2O2-production
MiPNet20.15 IsolationRatHeart-mt
MiPNet20.16 IOC105 Riga
MiPNet21.01 IOC109 Schroecken AT
MiPNet21.02 IOC111 Seattle WA US
MiPNet21.04 IOC110 Melbourne AU
MiPNet21.05 IOC108 Singapore SG
MiPNet21.06 SUIT RP
MiPNet21.07 MitoFit DatLab PT
MiPNet21.08 IOC107 Vienna AT
MiPNet21.09 IOC113 Havana CU
MiPNet21.10 IOC115 Schroecken AT
MiPNet21.11 IOC116 Innsbruck AT
MiPNet21.12 Comparison mt respiration media
MiPNet21.13 Comparison mt-preparations
MiPNet21.14 Reference sample HRR
MiPNet21.15 IOC112 Kuehtai AT
MiPNet21.16 DatLab 7 Innovations
MiPNet21.17 BloodCellsIsolation
MiPNet21.18 IOC117 Kuala Lumpur MY
MiPNet21.19 IOC114 Innsbruck AT
MiPNet22.01 IOC122 Schroecken AT
MiPNet22.02 IOC118 Hyderabad IN
MiPNet22.03 IOC119 Innsbruck AT
MiPNet22.04 IOC120 Barcelona ES
MiPNet22.05 National O2k-Workshop Shanghai CN
MiPNet22.06 IOC121 Cologne DE
MiPNet22.07 IOC124 Schroecken AT
MiPNet22.08 IOC123 Xian CN
MiPNet22.10 MiR05-Kit
MiPNet22.11 O2k-FluoRespirometer manual
MiPNet22.15 IOC125 Prague CZ
MiPNet22.16 DatLab 7 Innovations: DL-Protocols
MiPNet23.01 IOC126 Innsbruck AT
MiPNet23.02 IOC127 Szeged HU
MiPNet23.03 IOC128 Cambridge UK
MiPNet23.04 IOC133 Innsbruck AT
MiPNet23.06 IOC130 Schroecken AT
MiPNet23.07 IOC132 Budapest HU
MiPNet23.08 IOC134 Schroecken AT
MiPNet23.09 IOC136 Melbourne AU
MiPNet23.10 IOC129 Lausanne CH
MiPNet23.11 IOC137 Innsbruck AT
MiPNet23.12 DL-Protocols help
MiPNet23.13 IOC131 Kuala Lumpur MY
MiPNet23.14 IOC135 Busan KR
MiPNet23.15 O2k-pH ISE-Module
MiPNet24.01 IOC139 Schroecken AT
MiPNet24.02 IOC141 Schroecken AT
MiPNet24.03 IOC138 Xiamen CN
MiPNet24.04 IOC140 Amsterdam NL
MiPNet24.06 Oxygen flux analysis - DatLab 7.4
MiPNet24.08 Safranin Analysis Template
MiPNet24.09 Data analysis of mt-membrane potential
MiPNet24.10 H2O2 flux analysis
MiPNet24.11 mtMP calculation
MiPNet24.12 NextGen-O2k: Q-Module
MiPNet24.13 IOC142 Fukuoka JP
MiPNet24.14 O2k-sV-Module manual
MiPNet24.15 IOC143 Haryana IN
MiPNet24.16 DatLab8.0: CV-Module
MiPNet25.02 IOC Schroecken AT
MiPNet25.03 IOC144 Innsbruck AT
MiPNet25.04 IOC146 Padua IT
MiPNet25.06 IOC145 Innsbruck AT
MiPNet25.08 O2k-IQOQ protocol
MiPNet25.10 Distributor engagement Tokyo JP
MiPNet25.14 TPP Analysis Template
MiPNet25.16 Virtual O2k-Workshop HRR
MiPNet25.17 Virtual O2k-Workshop PhotoBiology
MiPNet26.02 Virtual O2k-Workshop:Q-Module
MiPNet26.06 DatLab 7: Guide
MiPNet26.07 Installation and startup support session
MiPNet26.10 MgG data analysis
MiPNet26.11 NextGen-O2k: PB-Module
MiPNet26.12 NextGen-O2k: NADH-Module
MiPNet26.13 NextGen-O2k manual
MiPNet26.14 Oxia
MiPNet27.01 IOC152 Hamburg DE
MiPNet27.02 IOC153 Innsbruck AT
MiPNet27.03 IOC154 Innsbruck AT
MiPNet27.04 IOC155 Schroecken AT
MiPNet27.05 Schroecken BEC tutorial-Living Communications pmP
MiPNet27.06 Prague BEC tutorial-Living Communications pmF
MiPNet27.07 Sample Holder
MiPNet27.08 Innsbruck BEC tutorial-Living Communications pmF
MiPNet27.09 FAT4BRAIN O2k-Workshop Schroecken AT
MiPNet27.10 IOC156 Ramat Gan IL
MiPNet28.01 IOC160 Schroecken AT
MiPNet28.02 IOC162 Schroecken AT
MiPNet28.03 IOC157 Los Angeles US
MiPNet28.05 IOC158 Innsbruck AT
MiPNet28.06 IOC161 Coimbra PT
MiPNet28.07 NextGen-O2k Series XB manual
MiPNet28.08 Oroboros O2k Series J manual
MiPNet28.09 O2k-Fluo Smart-Module manual
MiPNet28.10 SmartPOS-service
MiPNet28.11 IOC163 Schroecken AT
MiPNet28.12 IOC164 Schroecken AT
MiPNet28.13 IOC165 Innsbruck AT
MiPart
MiPschool Coimbra 2019
MiR05-Kit
MiR05-Kit.jpg

Mitochondrial Respiration Medium - MiR05-Kit, 1 vial; for a final volume of 250 mL

Microbalance 120 g
Microbalance 120 g.jpg

Microbalance max 120 g; 0.01 mg display; particularly for wet weight determination of permeabilized fibres.

Microbalance-Transport Case
Microbalance-Transport Case.jpg

Microbalance transport case, not suitable for shipping

Microsyringe\10 mm3 51/0.13 mm
Hamilton Syringes for Manual Titration.jpg

Hamilton Microsyringe\10 mm3 51/0.13 mm for manual titrations, 10 mm3 volume; fixed injection needle with rounded tip: 51 mm length, 0.13 mm inner diameter.

Microsyringe\100 mm3 51/0.41 mm
Microsyringe 100 mm3 51 0.41 mm - Kopie.JPG

Hamilton Microsyringe\100 mm3 51/0.41 mm for manual titrations, 100 mm3 volume; fixed needle with rounded tip: 51 mm length, 0.41 mm inner diameter. It is recommended for injections of suspensions of isolated mitochondria.

Microsyringe\200 mm3\TIP2k
Microsyringe200 mm3TIP2k.JPG

Microsyringe\200 mm3\TIP2k: Microinjection syringe for Titration-Injection microPump, 200 mm3 (碌l), fixed injection needle with rounded tip, with spacers.