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CS0390

Mitochondria Staining Kit

1 kit sufficient for 40 tests (of 5 mL cell suspensions), 1 kit sufficient for 200 tests (of 1 mL cell suspensions)

Synonym(e):

JC-1 dye

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Ihnen/SKUVerfügbarkeitPreis
1 kit
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€ 540,00

Über diesen Artikel

NACRES:
NA.32
UNSPSC Code:
12352207

€ 540,00


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Quality Segment

usage

 kit sufficient for 200 tests (of 1 mL cell suspensions),  kit sufficient for 40 tests (of 5 mL cell suspensions)

packaging

pkg of 1 kit

storage condition

dry at room temperature

technique(s)

flow cytometry: suitable, protein staining: suitable

fluorescence

λex 490 nm; λem 530 nm (green) (JC-1 monomers), λex 525 nm; λem 590 nm (red) (JC-1 aggregates)

application(s)

cell analysis
detection

detection method

fluorometric

shipped in

wet ice

storage temp.

2-8°C

General description

In normal cells, the JC-1 dye concentrates in the mitochondrial matrix where it forms red fluorescent aggregates. Any event that dissipates the mitochondrial membrane potential (e.g. apoptosis) prevents the accumulation of the JC-1 dye in the mitochondria and thus, the dye is dispersed throughout the entire cell leading to a shift from red (JC-1-aggregates) to green fluorescence (JC-1 monomers). The fluorescence of the cells stained with this kit may be observed by fluorescence microscopy or measured by fluorimetric and flow cytometry analysis.

Application

The dissipation of the mitochondrial electrochemical potential gradient (Δψ) is known as an early event in apoptosis. This kit offers a fast and convenient method for the detection of changes in mitochondrial inner-membrane electrochemical potential in living cells using the cationic, lipophilic dye, JC-1.

Features and Benefits

Kit offers:
  • A fast, simple, and convenient method for staining and assaying mitochondria intactness
  • Contains all the reagents required for the detection of changes mitochondrial inner-membrane electrochemical potential
  • Contains the antibiotic valinomycin, which can be used as a control agent that prevents JC-1 aggregation
  • The shift in fluorescence is clearly detectable in both green and red channels
  • Suitable for adherent cells as well as cells in suspension
  • Has been tested with Jurkat, U-937, HeLa, NIH3T3 cells
  • The fluorescence signal can be observed by fluorescence microscopy or measured by flow cytometry

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Dieser Artikel
CS0760APT142420200
technique(s)

flow cytometry: suitable, protein staining: suitable

technique(s)

flow cytometry: suitable, protein staining: suitable

technique(s)

flow cytometry: suitable

technique(s)

-

packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

-

packaging

-

application(s)

cell analysis
detection

application(s)

cell analysis
detection

application(s)

-

application(s)

-

fluorescence

λex 490 nm; λem 530 nm (green) (JC-1 monomers), λex 525 nm; λem 590 nm (red) (JC-1 aggregates)

fluorescence

λex 490 nm; λem 590 nm (JC-1 dye)

fluorescence

-

fluorescence

-

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

detection method

-


Nur Kit-Komponenten

Produkt-Nr.
Beschreibung

  • DMSO 1 mL

  • JC Staining Buffer 5X 120 mL

  • JC-1 1 mg

  • Valinomycin Ready Made .1 mL

Lagerklasse

10 - Combustible liquids

wgk

WGK 3



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Questions

  1. Do you know which product is suitable for evaluating the intactness of isolated mitochondria?

    1 answer
    1. You can use MTT to assess the intactness of isolated mitochondria. For this purpose, the CT01-5 Sigma-Aldrich MTT Reagent A is suitable. Additionally, the following publication may be of interest as a protocol reference: PLoS One. 2015 Jul 29;10(7):e0134139. This publication discusses the prevention of cisplatin-induced acute kidney injury and can provide valuable insights.

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