TMRE-Mitochondrial膜Potential Assay试剂盒
TMRE-Mitochondrial Membrane Potential Assay Kit
5
(4 Reviews)
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(242 Publications)
- Complete kit for TMRE staining with a full protocol and stock solutions of TMRE and FCCP control
- Cited in > 200 publications
- FuncS
Unknown
Functional Studies - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
Analysis of TMRE staining using a fluorescent plate reader and a microplate.
Chart showing mean fluorescent intensity +/- standard deviation from quadruplicate measurements of 400 nM TMRE stained Jurkat cells in a 96-well microplate +/- treatment with FCCP.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
A : HeLa cells (adherent) were cultured on coverslips and stained with ab113852 (200nM TMRE) for 20 minutes in media, washed briefly with PBS and immediately imaged. B : Jurkat cells (suspension) were stained and washed as above and then transferred to a slide and immobilized under a coverslip for imaging.
- FuncS
PubMed
Functional Studies - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
Mitochondrial membrane potential was measured using ab113852.
P19 neurons (750 cells/mm2) were exposed to MDMA on days 7–9 in serum-free medium for 10 min up to 48 hours. The positive control FCCP (carbonyl cyanide-p-trifluoromethoxyphenylhydrazone), an uncoupler of mitochondrial oxidative phosphorylation, was applied at the concentration of 5 μM for 10 min. The cells were incubated with 500 μM TMRE for 30–45 min at 37°C, 5% CO2, followed by washing once with 100 μl of HBSS containing 0.2% bovine serum albumin. A volume of 200 μL of HBSS containing 0.2% bovine serum albumin was added to each well, and the fluorescence was measured with excitation/emission : 544/590 nm.
Popova D et al., PloS One, 11(11). Fig 5. doi: 10.1371/journal.pone.0166750 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
- Flow Cyt
Supplier Data
Flow Cytometry - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
Flow cytometry histogram of Jurkat cells stained with ab113852 (100nM TMRE) with (blue) or without (red) treatment with 100µM FCCP.
- FuncS
PubMed
Functional Studies - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
TMRE assay to assess mitochondrial function after C. rodentium infection.
Maiti et al (2015) used TMRE assay kit ab113852 to assess mitochondrial membrane potential in murine distal colon after C. rodentium infection.
Image courtesy of Maiti A K et al. Sci Rep. 2015; 5: 1543. doi: 10.1038/srep15434. Reproduced under the Creative Commons License http://creativecommons.org/licenses/by/4.0/
- FuncS
PubMed
Functional Studies - TMRE-Mitochondrial Membrane Potential Assay Kit (AB113852)
Mitochondrial membrane potential assayed using TMRE in the study of VIP.
Maiti AK et al (2018) used TMRE assay kit ab113852 to measure mitochondrial membrane potential in an in vitro mouse intestinal model treated with cytokines in the presence and absence of VIP (vasoactive intestinal peptide). VIP was induced by C. rodentium infection and cytokines.
Image courtesy of Maiti A K et al. PLoS One. 2018; 13(9): e0204567. doi: 10.1371/journal.pone.0204567
产品详情
How the assay works
The TMRE Mitochondrial Membrane Potential Assay Kit uses a fluorescent dye called tetramethylrhodamine ethyl ester (TMRE).
TMRE (tetramethylrhodamine, ethyl ester) is used to label active mitochondria. TMRE is a cell permeant, positively-charged, red-orange dye that readily accumulates in active mitochondria due to their relative negative charge. Depolarized or inactive mitochondria have decreased membrane potential and fail to sequester TMRE. NB: TMRE is also available as free molecule as ab274305 (Tetramethylrhodamine ethyl ester).
The TMRE protocol also uses FCCP (carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone), which is a ionophore uncoupler of oxidative phosphorylation. Treating cells with FCCP eliminates mitochondrial membrane potential and TMRE staining. TMRE is suitable for the labeling of mitochondria in live cells and is not compatible with fixation.
TMRE assay protocol summary
- Add FCCP to appropriate control cell samples and incubate for 10 min
- Incubate with TMRE for 15-30 min, pellet (suspension cells) / remove media (adherent cells) and wash with PBS / 0.2% BSA
- Analyze with micro-plate reader at Ex/Em 549/575 nm, flow cytometer using 488nm laser for excitation and at emission 575 nm, or fluorescent microscope.
TMRE is only suitable for use with live (not fixed) cells.
How other researchers are using TMRE assay kit ab113852
TMRE-Mitochondrial Membrane Potential Assay Kit has been used in a variety of sample type including:
Human pulmonary arterial endothelial cells (PAECs) 1
Mice spermatozoa 2
Human adipose-derived mesenchymal stem cells (AD-MSCs) 3
References:
1-Piper B et al. 2024
2-Park S al. 2024
3-Abu-El-Rub E et al. 2023
Related and recommended products
See other alternative kits to quantify Mitochondrial Membrane Potential:
- JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) ab112134
- JC-10 Mitochondrial Membrane Potential Assay Kit (Flow Cytometry) ab112133
- JC-1 - Mitochondrial Membrane Potential Assay Kit ab113850
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推荐的短期储存条件
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储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The mitochondrial membrane potential drives ATP synthesis by powering ATP synthase an enzyme complex embedded in the mitochondrial membrane. This potential also plays a vital role in other processes such as calcium homeostasis and regulation of mitochondrial biogenesis. The mitochondrial membrane itself forms part of the larger mitochondrial respiratory chain complex coordinating with components like complex I (NADH: ubiquinone oxidoreductase) and complex II (succinate dehydrogenase) to maintain cell energy needs and respond to metabolic demands.
Pathways
The mitochondrial membrane potential is integral to cellular energy metabolism pathways such as the Krebs cycle and oxidative phosphorylation. Mitochondrial membrane potential modulation can affect signaling proteins like cytochrome c which is instrumental in apoptosis. Apoptotic signaling pathways involving proteins such as Bax and Bcl-2 influence the mitochondrial membrane potential and regulate cell survival or death in response to cellular stress or damage.
靶点信息
文献 (242)
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