Dead Cell Apoptosis Kits with Annexin V for Flow Cytometry
Dead Cell Apoptosis Kits with Annexin V for Flow Cytometry
Invitrogen™

Dead Cell Apoptosis Kits with Annexin V for Flow Cytometry

Assess cell viability with Dead Cell Apoptosis kits with Annexin V and conjugated fluorescent dyes such as Alexa Fluor 488, FITC, PI, PE, APC, and SYTOX Green.
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Catalog NumberQuantityLabel or Dye
V35112Promo Image1 KitSYTOX Green, R-PE
V13241Promo Image50 AssaysAlexa Fluor 488, Propidium Iodide
V13242Promo Image1 KitFITC, Propidium Iodide
V35113Promo Image1 KitSYTOX Green, APC
V13245Promo Image250 AssaysAlexa Fluor 488, Propidium Iodide
Catalog number V35112
Price (EUR)
598,65
Online Exclusive
798,00
Save 199,35 (25%)
1 kit
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Quantity:
1 Kit
Label or Dye:
SYTOX Green, R-PE
Price (EUR)
598,65
Online Exclusive
798,00
Save 199,35 (25%)
1 kit
Add to cart
Easily differentiate live, dead, and apoptotic cells during flow cytometry with our Dead Cell Apoptosis kits with Annexin V conjugates including Alexa Fluor 488, FITC, propidium iodide, PE, APC, and SYTOX Green. These conjugates distinguish live, dead, or apoptotic cells via different dyes, which is vital for confirming cell viability and apoptosis using multi-parametric studies.
There are several advantages to using Dead Cell Apoptosis kits with Annexin V for flow cytometry in order to assay cell viability:

Superior brightness
Unlike other Annexin V kits that have lower protein concentrations or purification levels, the Annexin V Alexa Fluor 488 conjugate is optimized for flow cytometry to provide the largest separation between apoptotic and live cells. The Alexa Fluor 488 dye is a superior green-fluorescent dye with a spectrum similar to fluorescein (FITC).

High binding efficiency
Annexin V conjugates are made from a highly purified cys-annexin, resulting in higher binding efficiency and extremely accurate characterization of the apoptotic process.

Multi-parametric
Many publications require a minimum of two different ways to identify apoptotic cells. This multi-parametric kit detects phosphatidyl serine (PS) on the cytoplasmic surface of the cell membrane, while membrane integrity is determined via propidium iodide.

Dead Cell Apoptosis Kit with Annexin V Alexa Fluor 488 & PI
The Dead Cell Apoptosis Kit with Annexin V Alexa Fluor 488 & Propidium Iodide (PI) (V13241, V13245) is used in flow cytometry to measure early apoptosis by detecting phosphatidyl serine (PS) expression and membrane permeability. When cells are stained with Annexin V and propidium iodide, apoptotic cells expressing PS show green fluorescence, which can be detected in the FITC channel, and low red fluorescence. Dead or necrotic cells show bright red fluorescence and no green fluorescence, while live cells show no green or red fluorescence.

Dead Cell Apoptosis Kit with Annexin V PE and SYTOX Green
The Dead Cell Apoptosis Kit with Annexin V PE and SYTOX Green detects PS externalization in apoptotic cells during flow cytometry using recombinant annexin V conjugated to the orange fluorescent phycobiliprotein R-PE, while dead cells are detected with SYTOX Green nucleic acid stain. After treatment with both probes, apoptotic cells show orange fluorescence, dead cells show green fluorescence, and live cells show little or no fluorescence. These populations can easily be distinguished in the 530/30 nm and 585/42 nm bandpass filters with a 488 nm laser flow cytometer.

Dead Cell Apoptosis Kit with Annexin V APC and SYTOX Green
The Dead Cell Apoptosis Kit with Annexin V APC and SYTOX Green detects PS externalization in apoptotic cells during flow cytometry using recombinant annexin V conjugated to red laser-excited allophycocyanin, and dead cells using SYTOX Green nucleic acid stain. Apoptotic cells are detected by annexin V binding to externalized PS. Live cells show little or no fluorescence, apoptotic cells show red fluorescence and very little green fluorescence, and late apoptotic cells show a higher level of red and orange fluorescence. These populations can easily be distinguished using a flow cytometer that has both 488 nm and 633 nm excitation sources (an argon-ion laser and a HeNe laser).

The Dead Cell Apoptosis Kit with Annexin V FITC and PI
The Dead Cell Apoptosis Kit with Annexin V FITC and PI detects PS externalization in apoptotic cells using recombinant annexin V conjugated to green-fluorescent FITC dye and dead cells using PI. Necrotic cells that stain with PI show red fluorescence. After treatment with both probes, apoptotic cells show green fluorescence, dead cells show red and green fluorescence, and live cells show little or no fluorescence.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
DescriptionDead Cell Apoptosis Kit with Annexin V PE and SYTOX™ Green, for flow cytometry
Excitation/Emission503, 488/524, 575
Flow Cytometer Laser Lines561, 488
For Use With (Equipment)Fluorescence Microscope, Flow Cytometer
Kit ContentsContains 1 vial of annexin V, R-PE conjugate (250 μL), 1 vial of SYTOX green stain (100 μL), and 1 bottle of annexin binding buffer (5X solution, 15 mL).
Label or DyeSYTOX Green, R-PE
No. of Reactions50
Product TypeApoptosis Detection Kit
Quantity1 Kit
Shipping ConditionWet Ice
Unit Size1 kit
Contents & Storage
Store in refrigerator (2°C to 8°C) and protect from light.

Frequently asked questions (FAQs)

How do SYTO dyes bind to DNA?

The binding mode of SYTO nucleic acid stains is unknown. However, the behavior of these and related nucleic acid dyes suggests the following binding properties:

1.They appear to contact the solvent (suggested by sensitivity to salt, divalent cations, and in particular, SDS) and thus are likely to have contacts in the grooves.
2.All SYTO dyes appear to show some base selectivity and are thus likely to have minor groove contacts.
3.They can be removed from nucleic acid via ethanol precipitation; this characteristic is not shared by ethidium bromide and other intercalators. Likewise, the dyes are not removed from nucleic acid via butanol or chloroform extraction. These extraction methods do remove ethidium bromide from nucleic acid. 4. SYTO binding is not affected by nonionic detergents.
5. SYTO dyes are not quenched by BrdU, so they do not bind nucleic acids in precisely the same way as Hoechst 33342 and DAPI ((4′,6-diamidino-2-phenylindole).

SYBR Green I has shown little mutagenicity on frameshift indicator strains, indicating that it isn't likely to strongly intercalate.

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

When using Dead Cell Apoptosis Kits with Annexin V for Flow Cytometry, what does a PI+ only population (hence Annexin V negative) correspond to?

These products are cells that died without undergoing apoptosis. A PI+ only population could be either a result of experimental condition or sample preparation.

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

Fluorescence spectra

Fluorescence spectra

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