APC Annexin V Apoptosis Detection Kit with 7-AAD

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Regulatory Status
RUO
Other Names
Annexin A5 Apoptosis Detection Kit
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Product Citations
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Annexin-V_APC-7AAD_Antibody_FC_1_050714.jpg
Human T-cell leukemia cell line, Jurkat, treated (top) or non-treated (bottom) with LEAF™ purified anti-human CD95 (clone EOS9.1) for 4 hours, then stained with APC Annexin V Apoptosis Detection Kit with 7-AAD.
  • Annexin-V_APC-7AAD_Antibody_FC_1_050714.jpg
    Human T-cell leukemia cell line, Jurkat, treated (top) or non-treated (bottom) with LEAF™ purified anti-human CD95 (clone EOS9.1) for 4 hours, then stained with APC Annexin V Apoptosis Detection Kit with 7-AAD.
  • Annexin-V_APC-7AAD_Antibody_FC_2_050714.jpg
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Description

BioLegend's APC Annexin V Apoptosis Detection Kit with 7-AAD has been specifically designed for the identification of apoptotic and necrotic cells.

Annexin V (or Annexin A5) is a member of the annexin family of intracellular proteins that binds to phosphatidylserine (PS) in a calcium-dependent manner. PS is normally only found on the intracellular leaflet of the plasma membrane in healthy cells, but during early apoptosis, membrane asymmetry is lost and PS translocates to the external leaflet. Fluorochrome-labeled Annexin V can then be used to specifically target and identify apoptotic cells. Annexin V Binding Buffer is recommended for use with Annexin V staining. Annexin V binding alone cannot differentiate between apoptotic and necrotic cells. To help distinguish between the necrotic and apoptotic cells we recommend use of our 7-amino-actinomycin D (7-AAD) solution. Early apoptotic cells will exclude 7-AAD, while late stage apoptotic cells will stain positively, due to the passage of these dyes into the nucleus where they bind to DNA.

7-AAD (7-amino-actinomycin D) has a high DNA binding constant and is efficiently excluded by intact cells. It is useful for DNA analysis and dead cell discrimination during flow cytometric analysis. When excited by 488 laser light, 7-AAD fluorescence is detected in the far red range of the spectrum (650 nm long-pass filter).

Product Details
Technical data sheet

Product Details

Verified Reactivity
Human, Mouse, Rat
Reported Reactivity
Other Species
Concentration
Lot-specific (to obtain lot-specific concentration and expiration, please enter the lot number in our Certificate of Analysis online tool.)
Storage & Handling
Store between 2°C and 8°C. Do not freeze.

Caution: 7-AAD is a potential carcinogen. It is recommended that the user wear protective clothing, gloves, and eye/face protection in order to avoid contact with skin and eyes.
Application

FC - Quality tested

Recommended Usage

Staining Procedure:
1. Wash cells twice with cold BioLegend's Cell Staining Buffer, and then resuspend cells in Annexin V Binding Buffer at a concentration of 0.25-1.0 x 107 cells/mL.
2. Transfer 100 µL of cell suspension in a 5 mL test tube.
3. Add 5 µL of APC Annexin V.
4. Add 5 µL of 7-AAD Viability Staining Solution.
5. Gently vortex the cells and incubate for 15 min at room temperature (25°C) in the dark.
6. Add 400 µL of Annexin V Binding Buffer to each tube. Analyze by flow cytometry with proper machine settings.

Excitation Laser
Red Laser (633 nm)
Application Notes

Materials Provided:
0.5 ml of APC Annexin V
0.5 ml of 7-AAD Viability Staining Solution
50 ml of Annexin V Binding Buffer

Materials Not Included:
Cell Staining Buffer (Cat. No. 420201)

For a better experience detecting apoptosis, we now recommend Apotracker™. Cell staining with Apotracker™ is Calcium independent. Thus, no special buffers are required, and the protocol can be shortened for single-step co-staining with other reagents.

Application References

(PubMed link indicates BioLegend citation)
  1. Maciel E, et al. 2014. Arch Biochem Biophys. 548:38. PubMed
Product Citations
  1. Català C, et al. 2022. iScience. 25:105078. PubMed
  2. Chiarella E, et al. 2020. Heliyon. 6:e04020. PubMed
  3. Chen CC, et al. 2020. Cancer Cell. 37:71. PubMed
  4. Paz H, et al. 2018. J Exp Clin Cancer Res. 37:67. PubMed
  5. Rutherford TR, et al. 2021. Cell Death Dis. 12:872. PubMed
  6. Fluckiger A, et al. 2016. Oncogene. 10.1038/onc.2015.523. PubMed
  7. Krone A, et al. 2022. Sci Rep. 218:. PubMed
  8. Papadas A, et al. 2022. Cell Rep. 40:111201. PubMed
  9. Cribioli E, et al. 2022. Front Immunol. 13:976628. PubMed
  10. Huangfu J, et al. 2021. Cell Death Dis. 12:386. PubMed
  11. Li W, et al. 2022. PeerJ. 10:e14086. PubMed
  12. Gómez-Aleza C, et al. 2020. Nat Commun. 4.857638889. PubMed
  13. Broggi A, et al. 2017. Nat Immunol. 18:1084. PubMed
  14. Wu L, et al. 2022. Theranostics. 12:842. PubMed
  15. Yao F, et al. 2021. Nat Commun. 12:7333. PubMed
  16. Lee A, et al. 2022. Int J Oncol. 60:. PubMed
  17. Chen X, et al. 2021. Theranostics. 11:3392. PubMed
  18. Xie J, et al. 2018. Oncol Lett. 16:157. PubMed
  19. Vogiatzi F, et al. 2022. Blood Adv. 6:4847. PubMed
  20. Dong Y, et al. 2020. J Leukoc Biol. 108:1711. PubMed
  21. Li H,et al. 2017. Sci Rep.. 10.1038/s41598-017-13471-4. PubMed
  22. Zhuo J, et al. 2021. Cell Death Dis. 12:1084. PubMed
  23. Wu H, et al. 2021. Cell Death Discov. 7:225. PubMed
  24. Lei J, et al. 2021. Theranostics. 4251:11. PubMed
  25. Tanaka T, et al. 2020. Sci Rep. 10:15169. PubMed
  26. Dolan M, et al. 2019. PLoS One. 14:e0220101. PubMed
  27. Tang Q, et al. 2021. Genes Dev. 35:528. PubMed
  28. Gong H, et al. 2019. EBioMedicine. 44:138. PubMed
  29. Hu M, et al. 2020. Cancer Immunol Res. 8:1150. PubMed
  30. Singh SK, et al. 2021. Oncogene. 40:6153. PubMed
  31. Wang Y, et al. 2022. Nat Commun. 13:6663. PubMed
  32. Fragoso MF, et al. 2022. Int J Mol Sci. 23:. PubMed
  33. Yin S, et al. 2015. Sci Rep. 5: 14432. PubMed
  34. Gunda V, et al. 2020. Cancers (Basel). 12:00. PubMed
  35. Riebeling T, et al. 2020. Cell Death Differ. . PubMed
  36. Peeters R, et al. 2022. Nat Commun. 13:5371. PubMed
  37. Leary N, et al. 2022. J Extracell Vesicles. 11:e12197. PubMed
  38. Tang J, et al. 2021. Front Genet. 12:666451. PubMed
  39. Gourvest M, et al. 2021. Leukemia. . PubMed
  40. Huang Z, et al. 2021. Am J Cancer Res. 4287:10. PubMed
  41. Tan H, et al. 2022. Acta Pharm Sin B. 12:2348. PubMed
  42. Seong BKA, et al. 2021. Cancer Cell. 39:1262. PubMed
  43. Li K, et al. 2021. J Exp Med. 218:. PubMed
  44. Zhan L, et al. 2021. Exp Ther Med. 22:1082. PubMed
  45. Hezkiy EE, et al. 2022. Cells. 11:. PubMed
  46. Simula L, et al. 2020. Cell Death Differ. 27:2749. PubMed
  47. Corso J, et al. 2016. Proc Natl Acad Sci U S A. 113: 5688 - 5693. PubMed
  48. Lei X, et al. 2022. Nat Commun. 13:3882. PubMed
  49. Jin X, et al. 2022. iScience. 25:104349. PubMed

Antigen Details

Biology Area
Apoptosis/Tumor Suppressors/Cell Death, Cell Biology, Cell Proliferation and Viability, Neuroscience
Gene ID
308 View all products for this Gene ID

Related FAQs

How is your Annexin made and what sequence does it cover?

It is made in E. coli, covering human aa Met1-Asp320.

How does pH and staining temperature affect Annexin V-Phosphatidylserine binding?

Annexin-Phosphatidylserine binding is lost below pH 5.2 and with prolonged incubation over a temperature of 42°C.

Why do I need to use Annexin V Binding Buffer?

Annexin V binding requires the presence of calcium in the solution.  So, we provide Annexin V Binding Buffer (cat # 422201), which is optimized for the best performance of Annexin V staining.

Can I use RPMI during Annexin V staining?

It is best to follow protocol as described on the product data sheet. Moreover, RPMI 1640 has a relatively high concentration of phosphate and low calcium ion concentration, which negatively impacts Annexin binding to its target phosphatidylserine (PS). Measurement of cell death by using Annexin V may also be significantly affected by time of incubation on ice, calcium concentration, and type of medium.

Can I freeze Annexin V conjugates?

It should not be frozen as it will lead to loss of biological activity due to dimerization.

Is Annexin V suitable for conjugation with the Maxpar® kit for CyTOF®?

Maxpar® Labeling kits require the protein to be partially reduced, so the metal chelate can be introduced through an SH group in the hinge region of the reduced antibody. Human Annexin V contains only one Cysteine which was reported to be chemically inactive. Thus, the Maxpar® labeling protocol would not work with Annexin V, unless a free –SH group can be introduced to Annexin V.  For more information regarding SH-mediated conjugation of Annexin V please consult published papers such as this one.

Go To Top Version: 3    Revision Date: 11.01.2023

For Research Use Only. Not for diagnostic or therapeutic use.

 

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Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
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