MitoTracker™ Dyes for Mitochondria Labeling
MitoTracker™ Dyes for Mitochondria Labeling
Invitrogen™

MitoTracker™ Dyes for Mitochondria Labeling

These mitochondria dyes are specially packaged in vials of 50 μg each to create freshly reconstituted dyes without the impact of freeze-thaw cycles to aid in a simplified sample prep for cell analysis workflow.
製品番号(カタログ番号)概要励起波長域
M22425MitoTracker™ Red FM581⁄644
M22426MitoTracker Deep Red FM644⁄665
M7512MitoTracker™ Red CMXRos579/599
M7513MitoTracker Red CM-H2Xros579⁄599
M7514MitoTracker™ Green FM490⁄516
M7510MitoTracker Orange CMTMRos554⁄576
M7511MitoTracker Orange CM-H2TMRos554⁄576
製品番号(カタログ番号) M22425
価格(JPY)
77,100
Each
お問い合わせください ›
概要:
MitoTracker™ Red FM
励起波長域:
581⁄644

Rosamine & carbocyanine-based staining dyes MitoTracker Orange CMTMRos, Red CMXRos, Orange CM-H2TMRos, Red CM-H2XRos, Red FM, Green FM, & Deep Red FM enable mitochondria visualization with fluorescent imaging. These mitochondria dyes are specially packaged in vials of 50 μg each to create freshly reconstituted dyes without the impact of freeze-thaw cycles to aid in a simplified sample prep for cell analysis workflow.

Rosamine-based MitoTracker dyes for mitochondria labeling

Cell-permeant MitoTracker probes stain active mitochondria in live cells for labeling and localization in fluorescent cell imaging. Our rosamine-based mitochondrial staining dyes include MitoTracker Orange CMTMRos, a derivative of tetramethylrosamine, and MitoTracker Red CMXRos, a derivative of X-rosamine. MitoTracker Orange CM-H2TMRos and MitoTracker Red CM-H2XRos are reduced, nonfluorescent versions of the rosamine-based MitoTracker dyes that fluoresce upon oxidation. The fluorescent signal from the rosamine-based MitoTracker dyes is retained in the mitochondria even after aldehyde fixation and detergent permeabilization, making these mitochondria dyes flexible for many workflows including applications that require subsequent processing such as immunocytochemistry or in situ hybridization. MitoTrackerRed and Orange are well suited for multicolor labeling experiments because their fluorescence is well resolved from the green fluorescence of other probes.

Carbocyanine-based MitoTracker dyes for mitochondria labeling

Cell-permeant MitoTracker dyes stain active mitochondria in live cells for mitochondrial labeling and localization in fluorescent cell imaging. The carbocyanine-based dyes MitoTracker Green FM and MitoTracker Red FM accumulate in active mitochondria but are not well-retained in mitochondria after aldehyde fixation. The carbocyanine-based MitoTracker Deep Red FM stains active mitochondrial in live cells and is well-retained in mitochondria after aldehyde fixation and subsequent permeabilization with detergents for applications that require subsequent processing such as immunocytochemistry or in situ hybridization. MitoTracker Red FM and MitoTracker Deep Red FM are well suited for multicolor labeling experiments because their red fluorescence is well resolved from the green fluorescence of other probes.

Benefits of using MitoTracker mitochondria labeling dyes

MitoTracker dyes are provided in vials of 50 μg of lyophilized powder ready for reconstitution. To label mitochondria, live cells are simply incubated with the MitoTracker probe of your choice. The mitochondrial staining dyes passively diffuse across the plasma membrane and accumulate in active mitochondria. The MitoTracker dyes are offered in a range of wavelengths and can be used for mitochondrial localization in multicolor experiments.

Conventional fluorescent stains such as tetramethylrosamine and rhodamine 123 are readily sequestered by active mitochondria and are reversible in dynamic membrane potential measurements as they easily wash out of cells upon loss in membrane potential. In contrast, MitoTracker dyes contain a mildly thiol-reactive chloromethyl moiety so that mitochondrial staining is retained if the mitochondrial membrane potential is lost, allowing many of the MitoTracker dyes to be retained during cell fixation.

Throughout the cell life cycle, mitochondria use oxidizable substrates to produce an electrochemical proton gradient across the mitochondrial membrane (whose potential is negative), resulting in ATP production. MitoTracker dyes are ideal probes for mitochondria staining in experiments studying the cell cycle or processes such as apoptosis and other end point assays. MitoTracker dyes are also available for flow cytometry applications (Cat. No. M46750, M46751, M46752, and M46753).

Related products for mitochondrial membrane potential

For studying dynamic mitochondria membrane potential specifically, we recommend using JC-1 (cationic carbocyanine dye, Cat. No. T3168) or TMRM (tetramethyl rhodamine methyl ester, Cat. No. I34361) dyes. The MitoProbe JC-1 Assay Kit (Cat. No. M34152) contains the JC-1 dye in addition to the potent mitochondrial membrane-potential disrupter, CCCP, which depolarizes the mitochondrial membrane. These reagents can provide compensatory controls to correctly compensate green-to-red fluorescence ratio. TMRM is used for the detection of dynamic measurement of mitochondrial membrane potential.

研究用途にのみご使用ください。診断目的には使用できません。
仕様
Red
概要MitoTracker™ Red FM
検出法蛍光
励起波長域581⁄644
使用対象 (装置)蛍光顕微鏡、フローサイトメーター、マイクロプレートリーダー
フォーマットSpecial packaging
製品ラインMitoTracker
数量20 x 50 μg
出荷条件室温
標識タイプFluorescent Dye
製品タイプ色素
SubCellular Localizationミトコンドリア
Unit SizeEach
組成および保存条件
フリーザー(-5°C∼-30°C)に保存し、遮光してください。

よくあるご質問(FAQ)

It looks like my Mitotracker dye is staining more than just the mitochondria. Why?

This is typically a result of using too high of a concentration of the Mitotracker dye. Most organic dyes are used in the low micromolar range. The MitoTracker dyes are used at a much lower concentration, around 50–200 nanomolar. Higher concentrations can cause background fluorescence and non-mitochondrial staining.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Can I use MitoTracker Red CMXRos dye in a plate reader to study mitochondrial membrane potential changes?

Yes, it has been done. A literature search will find numerous examples. However, be aware that plate readers are typically less sensitive than microscopes or flow cytometers, which means that the degree of change in fluorescence may not be as sensitive or easily detectable with a plate reader. Be sure to optimize label times and concentrations carefully.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Our facility does not allow flow cytometry of live cells. Can I fix the cells after staining with MitoTracker Red FM dye?

No, this wouldn't work as MitoTracker Red FM dye is not retained upon fixation. See Table 2 in this manual (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/mp07510.pdf).

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

After I labeled neurons with MitoTracker Red CMXRos, they are dead the next day. Is this expected?

The Mitotracker dyes should be imaged soon after staining because over time, those dyes can be toxic.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I am testing mitochondrial membrane potential, but my untreated cells are fluorescing, and I'm not seeing a significant difference in my test sample.

Regardless of which dye you use - tetramethylrhodamine, methyl ester (TMRM), JC-1 or MitoTracker - untreated cells will fluoresce. It's just that cells with reduced mitochondrial membrane potential will fluoresce less. It is the degree of change which is important. JC-1 dye not only changes intensity, but has a ratiometric spectral change in excitation and emission. It is very important to have an untreated control as well as a positive control treated with a mitochondrial membrane potential destabilizer, such as CCCP or FCCP. Most mitochondrial stains are only for use with live cells, as the signal will not be retained to the same degree with fixation.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用および参考文献 (42)

引用および参考文献
Abstract
Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fission.
Authors:Dagda RK, Cherra SJ, Kulich SM, Tandon A, Park D, Chu CT,
Journal:J Biol Chem
PubMed ID:19279012
'Mitochondrial dysregulation is strongly implicated in Parkinson disease. Mutations in PTEN-induced kinase 1 (PINK1) are associated with familial parkinsonism and neuropsychiatric disorders. Although overexpressed PINK1 is neuroprotective, less is known about neuronal responses to loss of PINK1 function. We found that stable knockdown of PINK1 induced mitochondrial fragmentation and autophagy ... More
Flow cytometric determination of mitochondrial membrane potential changes during apoptosis of T lymphocytic and pancreatic beta cell lines: comparison of tetramethylrhodamineethylester (TMRE), chloromethyl-X-rosamine (H2-CMX-Ros) and MitoTracker Red 580 (MTR580).
Authors:Jayaraman S
Journal:J Immunol Methods
PubMed ID:16256133
'The mitochondria-specific dyes, TMRE, H2-CMX-Ros and MTR580 were determined for their suitability to measure mitochondrial potential changes of the T cell leukemia cell line Jurkat and insulin-secreting beta cell line NIT-1 during apoptosis. Both freshly harvested Jurkat and NIT-1 cells induced to undergo apoptosis displayed poor retention of the potential-sensitive, ... More
Three novel Bid proteins generated by alternative splicing of the human Bid gene.
Authors:Renshaw SA, Dempsey CE, Barnes FA, Bagstaff SM, Dower SK, Bingle CD, Whyte MK
Journal:J Biol Chem
PubMed ID:14583606
'Bid, a BH3-only Bcl-2 protein, is activated by proteolytic cleavage exposing the BH3 domain, which then induces apoptosis by interacting with pro-apoptotic Bcl-2 family proteins (e.g. Bax and Bak) at the mitochondrial surface. The arrangement of domains within Bid suggested that Bid function might be regulated in part by alternative ... More
Ketamine induces toxicity in human neurons differentiated from embryonic stem cells via mitochondrial apoptosis pathway.
Authors:Bosnjak ZJ, Yan Y, Canfield S, Muravyeva MY, Kikuchi C, Wells CW, Corbett JA, Bai X,
Journal:Curr Drug Saf
PubMed ID:22873495
'Ketamine is widely used for anesthesia in pediatric patients. Growing evidence indicates that ketamine causes neurotoxicity in a variety of developing animal models. Our understanding of anesthesia neurotoxicity in humans is currently limited by difficulties in obtaining neurons and performing developmental toxicity studies in fetal and pediatric populations. It may ... More
Novel guanidine-containing molecular transporters based on lactose scaffolds: lipophilicity effect on the intracellular organellar selectivity.
Authors:Biswas G, Jeon OY, Lee WS, Kim DC, Kim KT, Lee S, Chang S, Chung SK,
Journal:Chemistry
PubMed ID:18770513
We have synthesized two lactose-based molecular transporters, each containing seven guanidine residues attached to the lactose scaffold through omega-aminocarboxylate linker chains of two different lengths, and have examined their cellular uptakes and intracellular and organellar localizations in HeLa cells, as well as their tissue distributions in mice. Both molecular transporters ... More