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GFP-Certified™ Apoptosis/Necrosis detection kit for microscopy and flow cytometry

 
ENZ-51002-25 1 Kit 132.00 USD
 
  • True multiplexing capabilities with GFP and other green fluorescent probes
  • Readily distinguishes between healthy, early apoptotic, late apoptotic and necrotic cells
  • Optimized for both fluorescence microscopy and flow cytometry applications
  • Suitable for death pathway analysis and drug/toxin studies
The transition from apoptosis to necrosis is a loosely defined continuum that necessitates recognition of the various stages of the process. The display of phosphatidylserine (PS) on the extracellular face of the plasma membrane remains a unifying hallmark of early apoptosis. Phospholipid-binding proteins such as Annexin V bind with a high affinity to PS, in the presence of Ca2+. Given that Annexin V is not cell permeable, the binding of externalized PS is selective for early apoptotic cells.
enz-51002
FIGURE: Apoptosis/necrosis induction in mitochondrial GFP-expressing HeLa cells. The Apoptosis Detection Reagent (Annexin V-Cyanine 3) and Necrosis Detection Reagent (Red) specifically detect cell state with clear spectral separation from mitochondria-associated GFP signal. Healthy cells (A), cells undergoing apoptosis (B), cells undergoing late-stage apoptosis (C), and necrotic cells (D). Induction with 2 μM Staurosporine was shown to be time-dependent, and yielded four distinct cell states after 4 hours.
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enz-51002

Product Specification

Quantity:25 assays
 
Kit/Set Contains:Apoptosis Detection Reagent (Annexin V-EnzoGold): 140 µL
Necrosis Detection Reagent (Red): 150 µL
Apoptosis Inducer (Staurosporine): 50 nmoles
Binding Buffer (10X): 1.5 mL
 
Long Term Storage:+4°C
 
Use/Stability:The reconstituted Apoptosis Inducer (Staurosporine) should be stored at -20°C. Supplied as lyophilized powder (50 nmoles). Should be reconstituted in 50 µl DMSO for a 1mM stock solution.
 
Handling:Protect from light.
 
Background / Technical Information:

For the Manual please click here.

 

Product Literature References

J. Immunology 183, (2009), Supplemental Information, Full Text
Cell Surface Externalization of Annexin A1 as a Failsafe Mechanism Preventing Inflammatory Responses during Secondary Necrosis: K.E. Blume; J. Immunology 183, 8138 (2009),

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