Mito-FerroGreen

Name: Mito-FerroGreen
Price: 510.00 USD

Catalog Number:

CFA1108222DOJ

Mfr. No.:

M489-10

Price:

$510

Size:

1 set(50 ug x 2)

Quantity:

Add to Cart:

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- Overview
  - It is reported that iron is the most abundant transition metal element within an organism and shows various physiological activities. Recently, free iron in living cells is getting attention because its high reactivity is suggested to be related to cellular damage or death. Free iron exists in its stable redox states, ferrous ion (Fe2+) and ferric ion (Fe3+). In living cells, it is considered that understanding the behavior of Fe2+ is more important than that of Fe3+ because of the intracellular reductive environment, metal transporters and water solubility of Fe2+. Mito-FerroGreen is a novel fluorescent probe for the detection of ferrous ion (Fe2+) in mitochondria where Fe-S clusters and heme proteins are synthesized, and enables live cell fluorescent imaging of intracellular Fe2+.
    
    Please contact us at for specific academic pricing.
    
    More Details
    
    Cellular Senescence and Mitochondrial Disfunction Due to Lipid Accumulation
    
    Ferroptosis
    
    Mitochondria Research
- Properties
  - Storage
    
    Store at -20 °C and protect from light
    
    Shipping
    
    ambient temperature
    
    * For research use only
- Applications
  - Application
    
    Iron in Mitochondria
- Reference
  - 1) T. Hirayama, S. Kadota, M. Niwa and H. Nagasawa,"A mitochondria-targeted fluorescent probe for selective detection of mitochondrial labile Fe(II)", Metallomics, 2018, DOI: 10.1039/C8MT00049B, "Ac-MtFluNox" mentioned in the journal is "Mito-FerroGreen".
    
    2) T. Issitt, E. Bosseboeuf, N. Winter, N. Dufton, G. Gestri, V. Senatore, A. Chikh, A. Randi, C. Raimondi, "Neuropilin-1 controls endothelial homeostasis by regulating mitochondrial function and iron-dependent oxidative stress via ABCB8", iScience., 2018,DOI: 10.1016/j.isci.2018.12.005
    
    3) E. E. Mon, F. Y. Wei, R. N. R. Ahmad, T. Yamamoto, T. Moroishi and K. Tomizawa, "Regulation of mitochondrial iron homeostasis by siderofexin 2 ", J Physiol Sci.,2018,doi:10.1007/s12576-018-0652-2.
    
    4) M. Fujimaki, N. Furuya, S. Saiki, T. Amo, Y. Imamichi and N. Hattori, "Iron supply via NCOA4-mediated ferritin degradation maintains mitochondrial functions", Mol. Cell. Biol.., 2019,doi: 10.1128/MCB.00010-19.
    
    5) K. Tomita, M. Fukumoto, K. Itoh, Y. Kuwahara, K. Igarashi, T. Nagasawa, M. Suzuki, A. Kurimasa and T. Sato, "MiR-7-5p is a key factor that controls radioresistance via intracellular Fe2+ content in clinically relevant radioresistant cells.", Biochem Biophys Res Commun.., 2019,doi: 10.1016/j.bbrc.2019.08.117.
    
    6) Y. Wang and M. Tang, "PM2.5 induces ferroptosis in human endothelial cells through iron overload and redox imbalance", Environ. Pollut., 2019, 264, doi: 10.1016/j.envpol.2019.07.105.
    
    7) KF. Yambire, C. Rostosky, T. Watanabe, D. Pacheu-Grau, S. Torres-Odio,A. Sanchez-Guerrero,O. Senderovich, EG. Meyron-Holtz,I.Milosevic, J. Frahm, AP. West and N. Raimundo, "Impaired lysosomal acidification triggers iron deficiency and inflammation in vivo.", Elife, 2019, 3, (8), doi:10.7554/eLife.51031.
    
    8) H. Nishizawa, M. Matsumoto, T. Shindo, D. Saigusa, H. Kato, K. Suzuki, M. Sato, Y. Ishii, H. Shimokawa and K. Igarashi, "Ferroptosis is controlled by the coordinated transcriptional regulation of glutathione and labile iron metabolism by the transcription factor BACH1", J. Biol. Chem., 2019,doi: 10.1074/jbc.RA119.009548.
    
    9)Y. akashima, A. Hayano and B. Yamanaka, "Metabolome analysis reveals excessive glycolysis via PI3K/AKT/mTOR and RAS/MAPK signaling in methotrexate-resistant primary CNS lymphoma-derived cells.", Clin. Cancer Res., 2020, DOI:10.1158/1078-0432.