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A list of all pages that have property "Description" with value "Select '''Mouse Control: Zoom''' in the Graph-menu or press [Ctrl+Z].". Since there have been only a few results, also nearby values are displayed.

Showing below up to 51 results starting with #1.

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  • Superoxide dismutase  + (Mammalian '''superoxide dismutase''' (SOD)Mammalian '''superoxide dismutase''' (SOD) exists in three forms, of which the Mn-SOD occurs in mitochondria (mtSOD, SOD2; 93 kD homotetramer) and many bacteria, in contrast to the Cu-Zn forms of SOD (cytosolic SOD1, extracellular SOD3 anchored to the extracellular matrix and cell surface). [[Superoxide]] anion (O<sub>2</sub><sup>•-</sup>) is a major [[reactive oxygen species]] (ROS) which is dismutated by SOD to [[oxygen]] and [[hydrogen peroxide | H<sub>2</sub>O<sub>2</sub>]].hydrogen peroxide | H<sub>2</sub>O<sub>2</sub>]].)
  • Manuscript template for MitoFit Preprints  + (Manuscripts template for [[MitoFit Preprints]] and [[Bioenergetics Communications]].)
  • Attached cells  + (Many cell types are grown in culture as '''attached cells''', such as endothelial or neuronal cells in a monolayer.)
  • Metabolic control analysis  + (Metabolic control analysis is a science foMetabolic control analysis is a science focused on the understanding of metabolic regulation and control. In metabolism, the reductionist approach has allowed us to know which enzymes, metabolites and genes are involved in a metabolic pathway but this is not enough to understand how it is controlled, resulting in poor results from attempts to increase the rates of selected metabolic pathways. The control of the metabolism is the capacity to alter the metabolic state in response to an external signal. With this definition in mind, we will assess the metabolic control in terms of the strength of any of the responses to the external factor without making the assumption about the function or purpose of that response[1].</br></br>====Bibliography:====</br></br>::1. David Fell. Frontiers in metabolism 2. Understanding the control of metabolism. Portland Press. 1997.ntrol of metabolism. Portland Press. 1997.)
  • MiPNet-Publication  + (MiPNet is the abbreviation for the OROBOROS Journal '''Mitochondrial Physiology Network''', including chapters of the [[O2k-Manual]], [[O2k-Procedures]], [[O2k-Workshops]], and other announcements, starting with MiPNet 01 in 1996. See also »[[MiPNet]].)
  • Communication - mitochondria and the patient  + (Mitochondria and the patient: communication between patients, medical professionals, scientists, and the public)
  • Substrate-uncoupler-inhibitor titration  + (Mitochondrial '''Substrate-uncoupler-inhibMitochondrial '''Substrate-uncoupler-inhibitor titration''' ('''SUIT''') [[MitoPedia: SUIT |protocols]] are used with [[mitochondrial preparations]] to study respiratory control in a sequence of coupling and substrates states induced by multiple titrations within a single experimental [[assay]].[[assay]].)
  • Hydrogen ion pump  + (Mitochondrial '''hydrogen ion pumps''' — fMitochondrial '''hydrogen ion pumps''' — frequently referred to as "proton pumps" — are large enzyme complexes (CI, CIII, CIV, ATP synthase) spanning the mt-inner membrane mtIM, partially encoded by mtDNA. [[Complex I|CI]], [[CIII]] and [[CIV]] are H<sup>+</sup> pumps that drive [[hydrogen ion]]s against the electrochemical [[protonmotive force]] ''pmF'' and thus generating the ''pmF'', driven by electron transfer from reduced substrates to oxygen. In contrast, [[ATP synthase]] (also known as CV) is a H<sup>+</sup> pump that utilizes the exergy of proton flow along the protonmotive force to drive phosphorylation of [[ADP]] to [[ATP]].P]].)
  • Malate dehydrogenase  + (Mitochondrial '''malate dehydrogenase''' iMitochondrial '''malate dehydrogenase''' is localized in the mitochondrial matrix and oxidizes [[malate]], generated from fumarate by fumarase, to [[oxaloacetate]], reducing NAD<sup>+</sup> to NADH+H<sup>+</sup> in the [[TCA cycle]]. Malate is added as a substrate in most [[N-pathway control state]]s.[[N-pathway control state]]s.)
  • Proton pump  + (Mitochondrial '''proton pumps''' are largeMitochondrial '''proton pumps''' are large enzyme complexes (CI, CIII, CIV, CV) spanning the inner mt-membrane, partially encoded by mtDNA. [[Complex I|CI]], [[CIII]] and [[CIV]] are proton pumps that drive [[proton]]s against the electrochemical [[protonmotive force]], driven by electron transfer from reduced substrates to oxygen. In contrast, [[ATP synthase]] (also known as CIV) is a proton pump that utilizes the energy of proton flow along the protonmotive force to drive phosphorylation of [[ADP]] to [[ATP]].[[ATP]].)
  • MiR06Cr  + (Mitochondrial respiration medium, '''MiR06Cr''', developed for oxygraph incubations of mitochondrial preparations - ''[[permeabilized muscle fibers]]''. MiR06Cr = [[MiR06]] + 20 mM [[Creatine|creatine]].)
  • MiR05Cr  + (Mitochondrial respiration medium, '''MiR05Cr''', developed for oxygraph incubations of mitochondrial preparations - ''[[permeabilized muscle fibers]]''. MiR05Cr = [[MiR05]] + 20 mM [[Creatine|creatine]].)
  • Mitochondrial respiration media: comparison  + (Mitochondrial respiratory capacity and conMitochondrial respiratory capacity and control are compared in different '''mitochondrial respiration media''', MiRs, to evaluate the quality of MiRs in preserving mitochondrial function and to harmonize results obtained in various studies using different MiRs. In some cases alterations of the formulation are incorporated to optimize conditions for the simultaneous measurement of multiple parameters, e.g. respiration and [[ROS]] production.[[ROS]] production.)
  • Hydrogen  + (Molecular '''hydrogen''' H<sub>2<Molecular '''hydrogen''' H<sub>2</sub> is a constituent of the air with a volume fraction of 0.00005. It is a colorless and odorless gas with a molecular mass of 2.016. Its pharmacological potential and effects on mitochondrial metabolism are discussed in various publications without complete evidence on the underlying mechanisms.ithout complete evidence on the underlying mechanisms.)
  • Scattering  + (Most biological samples do not consist simMost biological samples do not consist simply of pigments but also particles (e.g. cells, fibres, mitochondria) which scatter the [[incident light]]. The effect of '''scattering''' is an apparent increase in [[absorbance]] due to an increase in pathlength and the loss of light scattered in directions other than that of the detector. Two types of scattering are encountered. For incident light of wavelength ''λ'', Rayleigh scattering is due to particles of diameter < ''λ'' (molecules, sub-cellular particles). The intensity of scatter light is proportional to ''λ''<sup>4</sup> and is predominantly backward scattering. Mie scattering is caused by particles of diameter of the order of or greater than ''λ'' (tissue cells). The intensity of scatter light is proportional to 1/''λ'' and is predominantly forward scattering.ional to 1/''λ'' and is predominantly forward scattering.)
  • Volume of the solute  + (Most of the chemicals for SUIT protocol tiMost of the chemicals for SUIT protocol titrations are prepared by weighing the substance on the balance, transferring to a volumetric glass flask and adding solvent until the intended volume is reached. However, for practical reasons some of the chemical compounds are prepared by just adding the solvent instead of adjusting it's volume. For example, this approach is useful if the substance is very toxic. Then an arbitratry amount is taken, its mass determined on the balance without trying to reach a specific value and the necessary amount of solvent is added. Adding the solvent instead of adjusting its volume is also useful if small amounts are needed (e.g. 1 mL) or if the compound has to be prepared directly before using it like Pyruvate. In these cases the volume contributed by the solute was tested.lume contributed by the solute was tested.)
  • Carrier control titrations  + (Most of the nonpolar compounds have to be Most of the nonpolar compounds have to be diluted in organic solvents such as DMSO or acetonitrile in order to use them for the titrations in the SUIT protocols. However, the solvent (carrier) itself could affect the mitochondrial physiology and promote alterations that we need to take into account. For this reason, it is necessary to run in parallel to our treatment experiment a control experiment on which we will add a '''carrier control titration''' to test if it affects our sample or not.' to test if it affects our sample or not.)
  • Q  + (Multiple meanings of Q ::::» [[Coenzyme Q]] Q ::::» [[Charge]] ''Q'', ''Q''<sub>el</sub> ::::» [[Heat]] ''Q'', ''Q''<sub>th</sub>)
  • Nigericin  + (Nigericin is a H<sup>+</sup>/KNigericin is a H<sup>+</sup>/K<sup>+</sup> antiporter, which allows the electroneutral transport of these two ions in opposite directions across the mitochondrial inner membrane following the K<sup>+</sup> concentration gradient. In the presence of K<sup>+</sup>, nigericin decreases pH in the mitchondrial matrix, thus, almost fully collapses the transmembrane ΔpH, which leads to the compensatory increase of the electric [[Mitochondrial membrane potential|mt-membrane potential]]. Therefore, it is ideal to use to dissect the two components of the [[Protonmotive force|protonmotive force]], ΔpH and [[Mitochondrial membrane potential|mt-membrane potential]]. It is recommended to use the lowest possible concentration of nigericin, which creates a maximal mitochondrial hyperpolarization. In the study of [[Komlodi 2018 J Bioenerg Biomembr]], 20 nM was applied on brain mitochondria isolated from guinea-pigs using 5 mM [[Succinate|succinate]] in the [[LEAK respiration|LEAK state]] which caused maximum hyperpolarisation, but did not fully dissipate the transmembrane ΔpH. Other groups (Selivanov et al 2008; Lambert et al 2004), however, used 100 nM nigericin, which in their hands fully collapsed transmembrane ΔpH using succinate as a respiratory substrate on isolated rat brain and skeletal muscle in the [[LEAK respiration|LEAK state]].AK respiration|LEAK state]].)
  • Viruses and mitochondrial medicine  + (Not enough is known about '''viruses and mitochondrial medicine''', although several studies point towards a link between viral infection and mitochondrial dysfunction using high-resolution respirometry, with potential impact on drug development.)
  • Nuclear receptors  + (Nuclear receptors are ligand-dependent transcription factors.)
  • Equivalence  + (Numerical '''equivalence''' (symbol ≡) indicates that two quantities are numerically equal, even if the full meaning may be different. For instance: 1 ≡ 1·1 and 1 ≡ 1/1. In contrast to ≡, the symbol = indicates physicochemical [[equality]].)
  • O2k-Virtual Support  + (O2k-Virtual support includes 8 individual O2k-Virtual support includes 8 individual hours. Via a live video link, Oroboros experts guide you step-by-step on topics of your choice, such as O2k instrumental setup and service of the polarographic oxygen sensors (POS) for instrumental quality control, an essential component of HRR. This offers the opportunity to analyze and discuss your experimental [[DatLab]] files obtained with your O2k with the bioenergetics experts of Oroboros. It offers flexibility to participants and gives the option to choose virtual sessions that best fit individual needs.l sessions that best fit individual needs.)
  • BME cutoff points  + (Obesity is defined as a disease associatedObesity is defined as a disease associated with an excess of body fat with respect to a healthy reference condition. Cutoff points for [[body mass excess]], '''BME cutoff points''', define the critical values for underweight (-0.1 and -0.2), overweight (0.2), and various degrees of obesity (0.4, 0.6, 0.8, and above). BME cutoffs are calibrated by crossover-points of BME with established BMI cutoffs.oints of BME with established BMI cutoffs.)
  • Creative Commons Attribution License  + (Open Access preprints (not peer-reviewed) Open Access preprints (not peer-reviewed) and articles (peer-reviewed) distributed under the terms of the '''Creative Commons Attribution License''' allow unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited. © remains with the authors, who have granted the publisher license in perpetuity.anted the publisher license in perpetuity.)
  • Open - DatLab  + (Open a previously recorded [[DatLab]] file.)
  • Internationale Gesellschaft fuer Regenerative Mitochondrien-Medizin  + (Organizer of * [http://bioblast.at/index.Organizer of </br>* [http://bioblast.at/index.php/Klinische_MitochondrienMedizin_und_Umweltmedizin_2015 Klinische MitochondrienMedizin und Umweltmedizin 2015]</br>* [http://wiki.oroboros.at/index.php/Klinische_MitochondrienMedizin_und_Umweltmedizin_2016_Heidelberg_DE Klinische MitochondrienMedizin und Umweltmedizin 2016]</br>* [http://wiki.oroboros.at/index.php/Klinische_Mitochondrienmedizin_und_Umweltmedizin_2017_Heidelberg_DE Klinische MitochondrienMedizin und Umweltmedizin 2017]</br>* [[Clinical Mitochondria- and Environmental Medicine 2018 Heidelberg DE|Klinische MitochondrienMedizin und Umweltmedizin 2018]][[Clinical Mitochondria- and Environmental Medicine 2018 Heidelberg DE|Klinische MitochondrienMedizin und Umweltmedizin 2018]])
  • Pyruvate dehydrogenase complex  + (Oxidative decarboxylation of pyruvate is catalyzed by the '''pyruvate dehydrogenase complex''' in the mt-matrix, and yields acetyl-CoA.)
  • P/O ratio  + (P/O ratio stands for phosphate to atomic oxygen ratio, where P indicates phosphorylation of ADP to ATP (or GDP to GTP).)
  • Equality  + (Physicochemical '''equality''' (symbol =) indicates in an equation not only numerical [[equivalence]] (symbol ≡), but an identity of the full meaning.)
  • Intracellular oxygen  + (Physiological, '''intracellular oxygen pressure''' is significantly lower than air saturation under normoxia, hence respiratory measurements carried out at air saturation are effectively hyperoxic for cultured cells and isolated mitochondria.)
  • RT  + (RT indicates '''room temperature''' or 25 °C. ''RT'' is the [[gas constant]] ''R'' [kJ/mol] multiplied by absolute [[temperature]] ''T'' [K]. This is the motive force quantum in the amount format ([[Gnaiger 2020 BEC MitoPathways]]).)
  • Warburg effect  + (Recently, controversies had a renaissance Recently, controversies had a renaissance on the much neglected Crabtree effect (aerobic glycolysis in a large range of cells exposed to glucose or fructose, with fully functional mitochondria; Crabtree 1929; Gnaiger and Kemp 1990) versus the '''Warburg effect''' (loss of mitochondrial function inducing cancer and stimulating compensatory aerobic glycolysis in the presence of oxygen; Warburg 1956; see list of references for reviews). Today it is widely accepted that ‘''the Warburg effect is not consistent across all cancer types''’ (Potter et al 2016) and reprogramming of mitochondrial energy metabolism represents a functional adjustment of cancer cells (Schöpf et al 2020).tment of cancer cells (Schöpf et al 2020).)
  • NADH fluorescence  + (Reduced nicotinamide adenine dinucleotide ([[NADH]]) is amongst the [[intrinsic fluorophores]] and can be used as an intracellular indicator of hypoxia. The excitation wavelength is 340 nm and emission is at 460 nm.)
  • 2-Hydroxyglutarate  + (Reduction of [[oxoglutarate]]Reduction of [[oxoglutarate]] (2OG or alpha-ketoglutarate) to '''2-hydroxyglutarate''' (2HG) is driven by NADPH. 2HG is also formed in side reactions of [[lactate dehydrogenase]] and [[malate dehydrogenase]]. Millimolar 2HG concentrations are found in some cancer cells compared to , whereas side activities of lactate and malate dehydrogenase form submillimolar s-2-hydroxyglutarate (s-2HG). However, even wild-type IDH1 and IDH2, notably under shifts toward reductive carboxylation glutaminolysis or changes in other enzymes, lead to “intermediate” 0.01–0.1 mM 2HG levels, for example, in breast carcinoma compared with nanomolar concentrations in benign cells. 2HG is considered an important player in reprogramming metabolism of cancer cells. reprogramming metabolism of cancer cells.)
  • Publicly deposited protocols  + (Researchers need to be introduced into adhResearchers need to be introduced into adhering to '''publicly deposited protocols'''. [[Prespecified protocols |Prespecified]] and [[time-stamped protocols]] that are publicly deposited may help to save Millions of Euros that may otherwise be wasted on research that is lacking coherent standards.search that is lacking coherent standards.)
  • Oxygen flow  + (Respiratory '''oxygen flow''' is the oxygeRespiratory '''oxygen flow''' is the oxygen consumption per total [[system]], which is an [[extensive quantity]]. [[Flow]] is advancement of a transformation in a system per time [mol·s<sup>-1</sup>], when 'system' is defined as the experimental system (e.g. an open or closed chamber). Flow is distinguished from the size-specific quantity [[flux]] obtained by normalization of flow per volume of the experimental system [mol·s<sup>-1</sup>·m<sup>-3</sup>]. An experimental object, e.g. a living cell, may be considered as the 'experimental system'. Then oxygen flow per cell has the unit [mol·s<sup>-1</sup>·x<sup>-1</sup>], where [x] is the [[elementary unit]] for a [[count]]. Oxygen flow or respiration per cell [amol·s<sup>-1</sup>·x<sup>-1</sup>] = [pmol·s<sup>-1</sup>·Mx<sup>-1</sup>] is normalized for the cell count, distinguished from [[oxygen flux]] (e.g. per mg protein or wet mass). These are different forms of [[normalization of rate]].zation of rate]].)
  • Reverse electron flow from CII to CI  + (Reverse electron flow from CII to CI stimuReverse electron flow from CII to CI stimulates production of [[ROS]] when mitochondria are incubated with succinate without rotenone in the LEAK state at a high [[mt-membrane potential]]. Depolarisation of the mt-membrane potential (''e.g.'' after ADP addition to stimulate OXPHOS) leads to inhibition of RET and therefore, decrease of RET-initiated ROS production. RET can be also measured when mitochondria are respiring using [[Glycerophosphate |Gp]] without rotenone in the [[LEAK respiration|LEAK]] state. Addition of I<sub>Q</sub>-side inhibitors (ubiquinone-binding side of CI) of [[Complex I |CI]] usually block RET. The following SUIT protocols allow you to measure RET-initiated H<sub>2</sub>O<sub>2</sub> flux in [[mitochondrial preparations]]: [[SUIT-009]] and [[SUIT-026]].[[SUIT-026]].)
  • Rhodamine 123  + (Rhodamine 123 (Rh123) is an [[extrinsic fluorophores|extrinsic fluorophore]]Rhodamine 123 (Rh123) is an [[extrinsic fluorophores|extrinsic fluorophore]] and can be used as a probe to determine changes in [[Mitochondrial_membrane_potential|mitochondrial membrane potential]]. Rh123 is a lipophilic cation that is accumulated by mitochondria in proportion to Δ''ψ''<sub>mt</sub>. Using ethanol as the solvent, the excitation maximum is 511 nm and the emission maximum is 534 nm. The recommended excitation and emission wavelengths in PBS are 488 and 515-575 nm, respectively (Sigma-Aldrich). are 488 and 515-575 nm, respectively (Sigma-Aldrich).)
  • Bioblasts  + (Richard Altmann (1894) defined the 'elemenRichard Altmann (1894) defined the 'elementary organisms' as '''Bioblasts'''. He observed granula in cells stained with osmium and viewed ‘the protoplasm as a colony of bioblasts’. "Microorganisms and granula are at an equivalent level and represent elementary organisms, which are found wherever living forces are acting, thus we want to describe them by the common term bioblasts. In the bioblast, that morphological unit of living matter appears to be found." [[Altmann 1894 Verlag Von Veit & Comp|Altmann 1894]]; p. 141. </br></br>Altmann is thus considered as the discoverer of [[mitochondria]] (the granula), which constitute together with the microorganisms the ''bioblasts'' (the elementary organisms). Bioblasts are the aliens with permanent residence in our cells ([[Bioblasts#Bioblasts_.E2.80.93_the_aliens_with_permanent_residence_in_our_cells|Gnaiger 2010]]).oblasts#Bioblasts_.E2.80.93_the_aliens_with_permanent_residence_in_our_cells|Gnaiger 2010]]).)
  • Save - DatLab  + (Save a DatLab file.)
  • Save as - DatLab  + (Save as a DatLab file.)
  • Zenodo  + (Science Europe: "Zenodo is an open source Science Europe: "Zenodo is an open source and free repository for storing data, code, materials, and any research artefact. It was created by CERN and launched within the frame of the OpenAIRE project, commissioned by the European Commission. It aims at fostering free and easy access to scientific results, scientific data, software, and publications to all researchers."are, and publications to all researchers.")
  • ASAPbio  + (Science only progresses as quickly and effScience only progresses as quickly and efficiently as it is shared. But even with all of the technological capabilities available today, the process of publishing scientific work is taking longer than ever. '''ASAPbio''' (Accelerating Science and Publication in biology) is a scientist-driven nonprofit working to address this problem by promoting innovation and transparency in life sciences communication.</br>In 2015, ASAPbio founder Ron Vale published an analysis of the increasing time to first-author publication among graduate students at UCSF, and proposed a more widespread use of preprints in the life sciences as a potential solution.the life sciences as a potential solution.)
  • Substrate control state  + (See '''[[Electron-transfer-pathway state]]''')
  • ET-pathway substrate types  + (See '''[[Electron-transfer-pathway state]]''')
  • Physiological pathway-control state  + (See [[Electron-transfer-pathway state]].)
  • Fluorescent marker  + (See [[Extrinsic fluorophores]])
  • Delete points  + (Select '''Delete points''' in the [[Marks - DatLab |Mark information]] window to remove all data points in the marked section of the active plot. See also [[Interpolate points]] and [[Restore points]] or [[Recalculate slope]].)
  • Interpolate points  + (Select '''Interpolate points''' in the [[Marks - DatLab |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]].)
  • Recalculate slope  + (Select '''Recalculate slope''' (Recalc. slSelect '''Recalculate slope''' (Recalc. slope) in the [[Marks - DatLab |Mark information]] window to restore data points in the marked section of the active Flux / Slope plot, if [[Delete points]] or [[Interpolate points]] was used before. The entire plot is recalculated, such that other marked sections which may have been deleted are also restored. Compare [[Restore points]].[[Restore points]].)
  • Restore points  + (Select '''Restore points''' in the [[Marks - DatLab |Mark information]] window to restore data points in the marked section of the active signal plot, if [[Delete points]] or [[Interpolate points]] was used before. Compare [[Recalculate slope]].)
  • Manage setups and templates - DatLab  + (Setups and templates in DatLab can be renamed or deleted under '''Manage setups''' or '''Manage templates'''.)
  • Graph options - DatLab  + (Several display options can be applied to a DatLab graph under '''Graph options'''.)
  • Comma for separating a term and its abbreviation  + (Should we used a '''comma for separating aShould we used a '''comma for separating a term and its abbreviation''' in the text? The SI Brochure frequently does not use a comma. The comma might be added, if it helps to clarify the distinction between the term and its abbreviation. The example “reduced Q fraction, ''Q''<sub>r</sub>” – the sequence of Q and ''Q''<sub>r</sub> may be confusing without comma. There will always be examples, where it is not clear, if a comma is needed.l always be examples, where it is not clear, if a comma is needed.)
  • Multicomponent analysis  + (Similarly to the [[least squares method]]Similarly to the [[least squares method]], '''multicomponent analysis''' makes use of all of the data points of the spectrum in order to analyse the concentration of the component parts of a measured spectrum. To do this, two or more reference spectra are combined using iterative statistical techniques in order to achieve the best fit with the measured spectrum.e the best fit with the measured spectrum.)
  • Holode  + (Small entetic units are counted into the reference system on a balance opposite to the experimental system with the large sample, which in balance contains as many abstract units as the count of entetic units in the reference system.)
  • Sodium phosphate buffer  + (Sodium phosphate buffer, '''Na-PB''', for [[HRR]] with freeze-dried baker´s yeast.)
  • Spline  + (Some [[spectrofluorometer]]Some [[spectrofluorometer]] or [[spectrophotometer]] software offers the possibility of '''spline''' interpolation of the spectral data points. This makes use of a polynomial (the number of '''spline''' points is entered by the user) to interpolate the curve between the data points.rpolate the curve between the data points.)
  • Mitochondrial density  + (Specific '''mitochondrial density''' is ''Specific '''mitochondrial density''' is ''D<sub>mtE</sub>'' = ''mtE''·''m<sub>X</sub>''<sup>-1</sup> [mtEU·kg<sup>-1</sup>]. If the amount of mitochondria, ''mtE'', is expressed as mitochondrial mass, then ''D<sub>mtE</sub>'' is the mass fraction of mitochondria in the sample. If ''mtE'' is expressed as mitochondrial volume, ''V''<sub>mt</sub>, and the mass of sample, ''m<sub>X</sub>'', is replaced by volume of sample, ''V<sub>X</sub>'', then ''D<sub>mtE</sub>'' is the volume fraction of mitochondria in the sample.eplaced by volume of sample, ''V<sub>X</sub>'', then ''D<sub>mtE</sub>'' is the volume fraction of mitochondria in the sample.)
  • Resolution  + (Spectral resolution is a measure of the abSpectral resolution is a measure of the ability of an instrument to differentiate between two adjacent wavelengths. Two wavelengths are normally considered to be resolved if the minimum detector output signal (trough) between the two peaks is lower than 80 % of the maximum. The resolution of a [[spectrofluorometer]] or [[spectrophotometer]] is dependent on its [[bandwidth]].[[bandwidth]].)
  • Custom-made stoppers  + (Stoppers can be custom-made for applications with user-specific sensors according to customer specifications.)
  • Tartronic acid  + (Tartronic acid (hydroxymalonic acid, C3H4O5; molecular weight 120.06) is an inhibitor of [[malic enzyme]].)
  • Taurine  + (Taurine, or 2-Aminoethan sulfonic acid, isTaurine, or 2-Aminoethan sulfonic acid, is one of the most abundant low-molecular-weight organic constituents in animals and humans. It has a multitude of functions in different types of tissue, one of which is the stabilization of membranes. Because of this and its antioxidative effect, taurine is a component of the respiration media MiR05 and MiR06 to preserve mitochondrial function. MiR06 to preserve mitochondrial function.)
  • Chinese Society of Mitochondrial Research and Medicine  + (The '''Chinese Society of Mitochondrial Research and Medicine''' (Chinese-Mit) is a member of [[Asian Society for Mitochondrial Research and Medicine|ASMRM]].)
  • Crabtree effect  + (The '''Crabtree effect''' describes the obThe '''Crabtree effect''' describes the observation that respiration is frequently inhibited when high concentrations of glucose or fructose are added to the culture medium - a phenomenon observed in numerous cell types, particularly in proliferating cells, not only tumor cells but also bacteria and yeast. The Pasteur effect (suppression of glycolysis by oxygen) is the converse of the Crabtree effect (suppression of respiration by high concentration of glucose or fructose).igh concentration of glucose or fructose).)
  • Default label  + (The '''Default label''' is the system default value for the axis label. These labels are changed automatically, according to the selected channel and unit. To change this label enter a [[Custom label]].)
  • Directory of Open Access Journals  + (The '''Directory of Open Access Journals''' is a free online directory that indexes and provides access to open access peer-reviewed journals.)
  • Exclusion criteria  + (The '''Exclusion criteria''' include factors or characteristics that make the recruited population ineligible for the outcome parameter. With the [[Inclusion criteria]], this factor must be a cofounder for the outcome parameter)
  • Faraday constant  + (The '''Faraday constant''' ''F'' links theThe '''Faraday constant''' ''F'' links the electric charge [C] to amount [mol], and thus relates the [[electrical format]] <u>''e''</u> [C] to the [[molar format]] <u>''n''</u> [mol]. The Farady constant, ''F'' = ''e''·''N''<sub>A</sub> = 96 485.33 C/mol, is the product of [[elementary charge]], ''e'' = 1.602176634∙10<sup>-19</sup> C/x, and the [[Avogadro constant]], ''N''<sub>A</sub> = 6.02214076∙10<sup>23</sup> x/mol. The dimensionless unit [x] is not explicitely considered by IUPAC.= 6.02214076∙10<sup>23</sup> x/mol. The dimensionless unit [x] is not explicitely considered by IUPAC.)
  • Inclusion criteria  + (The '''Inclusion criteria''' are based on The '''Inclusion criteria''' are based on key features of the target population that the researchers will use to answer their question. These criteria should identify the study population in a consistent, reliable, uniform, and objective manner. With the [[Exclusion criteria]], this factor must be a cofounder for the outcome parametert be a cofounder for the outcome parameter)
  • International Standard Serial Number  + (The '''International Standard Serial NumbeThe '''International Standard Serial Number''', ISSN, is a code used to identify periodical publications, independent of which media are used (print and/or electronic). - [[Bioenergetics Communications]], BEC: [https://portal.issn.org/resource/ISSN/2791-4690 ISSN 2791-4690]rg/resource/ISSN/2791-4690 ISSN 2791-4690])
  • International System of Units  + (The '''International System of Units''' (SThe '''International System of Units''' (SI) is the modern form of the metric system of [[unit]]s for use in all aspects of life, including international trade, manufacturing, security, health and safety, protection of the environment, and in the basic science that underpins all of these. The system of quantities underlying the SI and the equations relating them are based on the present description of nature and are familiar to all scientists, technologists and engineers. </br></br>The definition of the SI units is established in terms of a set of seven defining constants. The complete system of units can be derived from the fixed values of these defining constants, expressed in the units of the SI. These seven defining constants are the most fundamental feature of the definition of the entire system of units. These particular constants were chosen after having been identified as being the best choice, taking into account the previous definition of the SI, which was based on seven base units, and progress in science (p. 125).e units, and progress in science (p. 125).)
  • International Union of Pure and Applied Chemistry, IUPAC  + (The '''International Union of Pure and AppThe '''International Union of Pure and Applied Chemistry''' (IUPAC) celebrated in 2019 the 100<sup>th</sup> anniversary, which coincided with the [https://iupac.org/united-nations-proclaims-international-year-periodic-table-chemical-elements/ International Year of the Periodic Table of Chemical Elements (IYPT 2019)]. IUPAC {''Quote''} notes that marking Mendeleev's achievement will show how the periodic table is central to connecting cultural, economic, and political dimensions of global society “through a common language” {''end of Quote''} (Horton 2019). 2019 is proclaimed as the [https://iupac.org/united-nations-proclaims-international-year-periodic-table-chemical-elements/ International Year of the Periodic Table of Chemical Elements (IYPT 2019)]. For a '''common language''' in mitochondrial physiology and bioenergetics, the IUPAC ''Green book'' (Cohen et al 2008) is a most valuable resource, which unfortunately is largely neglected in bioenergetics textbooks. Integration of [[ergodynamics |open systems and non-equilibrium thermodynamic]] approaches remains a challenge for developing a common language (Gnaiger 1993; [[BEC 2020.1]]).C 2020.1]]).)
  • Korean Society of Mitochondrial Research and Medicine  + (The '''Korean Society of Mitochondrial Research and Medicine''' (KSMRM) is a member of [[Asian Society for Mitochondrial Research and Medicine|ASMRM]].)
  • MitoFit DOI Data Center  + (The '''MitoFit DOI Data Center''' is respoThe '''MitoFit DOI Data Center''' is responsible for the provision of digital identifiers, for the storage and ensuring the persistence of the scientific objects, the provision of access, review process and maintenance of the Metadata, and quality control.ance of the Metadata, and quality control.)
  • Mitochondrial Physiology Network  + (The '''Mitochondrial Physiology Network''' is the on-line Oroboros journal.)
  • N/NS pathway control ratio  + (The '''N/NS [[pathway control ratio]]The '''N/NS [[pathway control ratio]]''' is obtained when succinate is added to N-linked respiration in a defined coupling state. N and NS are abbreviations for respiration in the [[N-pathway control state]] (with pyruvate, glutamate, malate, or other ETS competent N-linked substrate combinations) and the [[NS-pathway control state]] (N in combination with succinate). NS indicates respiration with a cocktail of substrates supporting the N- and S-pathways.bstrates supporting the N- and S-pathways.)
  • N/S pathway control ratio  + (The '''N/S [[pathway control ratio]]The '''N/S [[pathway control ratio]]''' is obtained from SUIT protocols when the [[N-pathway control state |N-pathway flux]] and [[S-pathway control state |S-pathway flux]] are measured in the same [[coupling control state]]. The N/S pathway control ratio may be larger or smaller than 1.0, depending on the mitochondrial source and various mitochondrial injuries. The S-pathway control state may be selected preferentially as reference state, if mitochondria are studied with respect to N-pathway injuries.tudied with respect to N-pathway injuries.)
  • NS-N pathway control efficiency  + (The '''NS-N [[pathway control efficiency]]''', ''j''<sub>NS-N</sub> = 1-N/NS, expresses the fractional change of flux when succinate is added to the [[N-pathway control state]] in a defined [[coupling-control state]].)
  • NS-S pathway control efficiency  + (The '''NS-S pathway control efficiency''' The '''NS-S pathway control efficiency''' expresses the relative stimulation of succinate supported respiration (S) by NADH-linked substrates (N), with the [[S-pathway control state]] as the [[background state]] and the [[NS-pathway control state]] as the [[reference state]]. In typical [[SUIT protocol]]s with [[Electron-transfer-pathway state |type N and S substrates]], flux in the [[NS-pathway control state]] NS is inhibited by [[rotenone]] to measure flux in the [[S-pathway control state]], S(Rot) or S. Then the NS-S pathway control efficiency in the ET-coupling state is</br> ''j''<sub>(NS-S)''<sub>E</sub>''</sub> = (NS''<sub>E</sub>''-S''<sub>E</sub>'')/NS''<sub>E</sub>''</br>The NS-S pathway control efficiency expresses the fractional change of flux in a defined [[coupling-control state]] when inhibition by [[rotenone]] is removed from flux under S-pathway control in the presence of a type N substrate combination. Experimentally rotenone Rot is added to the NS-state. The reversed protocol, adding N-substrates to a S-pathway control background does not provide a valid estimation of S-respiration with succinate in the absence of Rot, since [[oxaloacetate]] accumulates as a potent inhibitor of [[succinate dehydrogenase]] CII.[[succinate dehydrogenase]] CII.)
  • O2k signal line  + (The '''O2k signal line''' is underneath thThe '''O2k signal line''' is underneath the [[O2k status line]]. It shows, depending on the [[O2k series]], on the left side the O2k number, the time of the experiment, the oxygen raw signal of each chamber, the [[block temperature]], the [[barometric pressure]], the Peltier power, the recorded amperometric and potentiometric raw signal, the enviromental (room) temperature and the signal from internal sensors recording the humidity and temperature of the electronics. On the right side of the O2k signal line the current [[User code - DatLab|user]], the DatLab version and the [[O2k serial number]] are displayed.[[O2k serial number]] are displayed.)
  • O2k-Accessory Box  + (The '''O2k-Accessory Box''' contains components of the [[POS-Service Kit]] and the [[O2k-Assembly Kit]] and is shipped with the O2k.)
  • O2k-Assembly Kit  + (The '''O2k-Assembly Kit''' is a component The '''O2k-Assembly Kit''' is a component of the [[Oroboros O2k]], consisting of 2 [[Stirrer-Bar\white PVDF\15x6 mm|PVDF Stirrer-Bars]], 2 [[PEEK]] O2k-Stoppers, [[OroboPOS-Connector]]s for O2k-series A-I and NextGen-O2k series XA (attached to the [[O2k-Main Unit]]) and cables (power supply, USB-connection). Several components of the O2k-Assembly Kit are included in the [[O2k-Accessory Box]] either for shipment or for storage.[[O2k-Accessory Box]] either for shipment or for storage.)
  • O2k-Fluo Smart-Module  + (The '''O2k-Fluo Smart-Module''' is an ampeThe '''O2k-Fluo Smart-Module''' is an amperometric add-on module to the [[Startup_O2k-Respirometer| O2k-Respirometer]], adding a new dimension to high-resolution respirometry. Optical sensors are inserted through the front window of the O2k-glass chambers, for measurement of hydrogen peroxide production (Amplex® UltraRed), ATP production (Magnesium Green™), mt-membrane potential (Safranin, TMRM), Ca<sup>2+</sup> (Calcium Green™), and numerous other applications open for O2k-user innovation. </br></br>::: » [[MiPNet28.09 O2k-Fluo Smart-Module manual]]et28.09 O2k-Fluo Smart-Module manual]])
  • O2k-Main Basic  + (The '''O2k-Main Basic''' is an integral elThe '''O2k-Main Basic''' is an integral element of the [[O2k-Main Unit]]. The Oroboros O2k Main Basic has the following components:</br>*Stainless-Steel Housing</br>*Switching power supply</br>*Microprocessor for integrated control, A/D converters and data handling</br>*Copper-Block with windows to 2 O2k-Chambers</br>*2 Amperometric OroboPOS Plugs</br>*TIP2k socket, providing the basis for add-on of the [[TIP2k]]</br>*2 Potentiometric Plugs for ion sensitive electrodes (ISE: TPP+, Ca2+; pH), providing the basis for add-on of the [[O2k-MultiSensor]] Modules</br>*2 Amperometric Plugs, providing the basis for add-on of the [[O2k-Fluo LED2-Module]] or NO (H<sub>2</sub>S) sensors.</br>*USB-Port for connection with DatLab (PC or laptop not included)for connection with DatLab (PC or laptop not included))
  • O2k-Main Unit  + (The '''O2k-Main Unit''' is a component of The '''O2k-Main Unit''' is a component of the [[O2k-Core]]. The O2k-Main Unit consists of functionally defined, integral elements, the ([[O2k-Main Basic]], [[O2k-Peltier Temperature Control]], two [[O2k-Electromagnetic Stirrer Twin-Control]] units, two [[O2k-Amperometric OroboPOS Twin-Channel]]s, [[O2k-Barometric Pressure Transducer]]), which cannot be obtained separately.[[O2k-Barometric Pressure Transducer]]), which cannot be obtained separately.)
  • O2k chamber volume calibration  + (The '''O2k-chamber volume calibration''' has to be done before getting started with the [[Oroboros O2k]] to guarantee a standard [[chamber volume]] of 2.0 mL.)
  • O2k-ticket system  + (The '''O2k-ticket system''' is a customer The '''O2k-ticket system''' is a customer support platform based on Zammad. This system automatically attributes an unique Ticket number (which is visible on the subject of your e-mail) to each received customer inquiry. For an easy follow-up, all the related correspondence is collected under this Ticket number. </br></br>* Contact us: '''[email protected]'''</br></br>In order to provide a helpful and reliable support regarding your O2k/equipment, we suggest to include in your inquiries:</br></br>* your affiliation and your O2k-serial number - ''See'': [[O2k_series]]</br></br>* DLD file(s) with your reported issue accompanied by a brief explanation. issue accompanied by a brief explanation.)
  • Oxygen sensor test  + (The '''O<sub>2</sub> sensor teThe '''O<sub>2</sub> sensor test''' is an important component of [[MitoPedia: Oroboros QM |Oroboros Quality Management]]. The [[OroboPOS]] test is described in detail in [[MiPNet06.03 POS-calibration-SOP]], is performed after switching on the [[Oroboros O2k]], and is required as a basis of technical service of the instrument.red as a basis of technical service of the instrument.)
  • OXPHOS International  + (The '''OXPHOS International''' web portal is a repository of information useful to scholars studying mitochondria. The site is operated as a private "special interests" community hub.)
  • Oroboros USB-flash drive  + (The '''Oroboros USB-flash drive''' is deliThe '''Oroboros USB-flash drive''' is delivered with the [[Oroboros O2k]]. Copy the folder "Oroboros O2k-Course on HRR" from the '''Oroboros USB-flash drive''' to your computer. This folder contains the DatLab installation program as well as tools to find topics, O2k-manuals and O2k-protocols with corresponding DatLab demo files and templates for training with [[DatLab]].[[DatLab]].)
  • Q-redox state  + (The '''Q-redox state''' reflects the redoxThe '''Q-redox state''' reflects the redox status of the [[Q-junction]] in the mitochondrial or chloroplast [[ETS|electron transfer system (ETS)]]. [[Coenzyme Q]] (CoQ or Q, [[ubiquinone]]) is a mobile redox component located centrally in the mitochondrial [[ETS]], while plastoquinones are essential mobile components in the photosynthetic system with a similar function. The Q-redox state depends on the balance between reducing capacities of convergent electron entries from fuel substrates into the Q-junction and oxidative capacities downstream of Q to the electron acceptor oxygen. Therefore, deficiencies in the mitochondrial [[ETS]], originating from e.g. the malfunction of respiratory Complexes, can be detected by measuring the changes of the Q-redox state with respect to the respiratory activity.</br></br>A three-electrode system was implemented into the NextGen-O2k to monitor the Q-redox state continuously and simultaneously with respiratory oxygen consumption. Added CoQ2 reflects the mitochondrial Q-redox state when equilibrating both with the detecting electrode and the biological sites (e.g. Complexes I, II and III).ical sites (e.g. Complexes I, II and III).)
  • S/NS pathway control ratio  + (The '''S/NS [[pathway control ratio]]The '''S/NS [[pathway control ratio]]''' is obtained when [[rotenone]] (Rot) is added to the [[NS-pathway control state]] in a defined [[coupling control state]]. The reversed protocol, adding N-type substrates to a [[S-pathway control state]] as the [[background state]] does not provide a valid estimation of S-linked respiration with succinate in the absence of Rot, since [[oxaloacetate]] accumulates as a potent inhibitor of [[succinate dehydrogenase]] (CII).[[succinate dehydrogenase]] (CII).)
  • SUIT protocol pattern  + (The '''SUIT protocol pattern''' describes the type of the sequence of coupling and substrate control steps in a SUIT protocol, which may be liner, orthogonal, or diametral.)
  • Science Citation Index  + (The '''Science Citation Index''' SCI offers bibliographical access to a curated collection of journals across 178 scientific disciplines. The SCI provides gold-standard lists of established journals.)
  • SUIT protocol library  + (The '''Substrate-uncoupler-inhibitor titraThe '''Substrate-uncoupler-inhibitor titration (SUIT) protocol library''' contains a sequential list of SUIT protocols (D001, D002, ..) with links to the specific SUIT pages. Classes of [[SUIT|SUIT protocols]] are explained with coupling and substrate control defined for [[mitochondrial preparations]].[[mitochondrial preparations]].)
  • Taiwan Society for Mitochondrial Research and Medicine  + (The '''Taiwan Society for Mitochondrial Research and Medicine''' (TSMRM) is a member of [[Asian Society for Mitochondrial Research and Medicine|ASMRM]].)
  • USB port  + (The '''USB port''' describes the connection between O2k and Computer. With the USB cable connected, select '''USB port''' in the [[Connection window]]. Depending on the O2k series, it is possible to connect with a '''USB port''' or [[Serial port]].)
  • Abscissa  + (The '''abscissa''' is the horizontal axis The '''abscissa''' is the horizontal axis ''x'' of a rectangular two-dimensional graph with the [[ordinate]] ''y'' as the vertical axis. Values ''X'' are placed horizontally from the origin.</br></br>See [[Abscissal X/Y regression |Abscissal ''X''/''Y'' regression]].[[Abscissal X/Y regression |Abscissal ''X''/''Y'' regression]].)