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Apotracker™ Tetra Alexa Fluor® 647

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Regulatory Status
RUO
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1. Apotracker-Tetra_Alexa-Fluor-647_053123
Heat induced 40% dead C57BL/6 splenocytes stained with Helix NP™ Blue and Apotracker™ Tetra Alexa Fluor® 647 (left) or Alexa Fluor® 647 Streptavidin (right).
  • 1. Apotracker-Tetra_Alexa-Fluor-647_053123
    Heat induced 40% dead C57BL/6 splenocytes stained with Helix NP™ Blue and Apotracker™ Tetra Alexa Fluor® 647 (left) or Alexa Fluor® 647 Streptavidin (right).
  • 2. Apotracker-Tetra-Alexa-Fluor-647_111124
    Extracellular vesicles (50-300 nm) were isolated from human plasma and stained with anti-human CD81 (clone 5A6) PE/Cyanine7 and Apotracker™ Tetra Alexa Fluor® 647 (left) or stained with anti-human CD81 (clone 5A6) PE/Cyanine7 only (right). Data shown was gated on events within the 100-250 nm size range.
  • 3. Apotracker-Tetra-Alexa-Fluor-647_3_111224
    Extracellular vesicles (50-300 nm) were isolated from human plasma and stained with anti-human CD9 (clone HI9a) APC/Fire 750™ and Apotracker™ Tetra Alexa Fluor® 647 (left) or stained with anti-human CD9 (clone HI9a) APC/Fire 750™ only (right). Data shown was gated on events within the 100-250 nm size range.
Cat # Size Price Quantity Check Availability Save
427405 20 tests 76€
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427406 100 tests 236€
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Description

Apoptotic and/or necrotic cells display phosphatidylserine (PS) on their outer cell surface, where it acts as an ‘eat-me’ signal and contributes to efficient removal of dead cells by macrophages and other phagocytes. 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. Apotracker™ monomer binds to PS for the detection and removal of dead or dying cells which are effective and preferably at the same time buffer-independent (Calcium free buffer) in comparison to the agents used in the market thus far.

Product Details
Technical Data Sheet (pdf)

Kit Contents

Kit Contents

For Cat# 427405

  • 20 µL Apo-Monomer solution
  • 24 µL Alexa Fluor® 647 Streptavidin solution

For Cat# 427406

  • 100 µL Apo-Monomer solution
  • 120 µL Alexa Fluor® 647 Streptavidin solution

Product Details

Verified Reactivity
Human, Mouse
Formulation
Apo-Monomer: HEPES buffered saline w/ 8% Glycerol, pH 7.4

Streptavidin: Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
Preparation
The Apo monomer was purified by affinity chromatography and conjugated with biotin under optimal conditions. Streptavidin was conjugated with Alexa Fluor® 647 under optimal conditions.
Storage & Handling
Kit components should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

FC - Quality tested
Recommended Usage

Each lot of this product is quality control tested by immunofluorescent staining with flow cytometric analysis. The suggested use of this reagent is 5 µL of the Apo-Monomer + Streptavidin-Fluorophore mixture per million cells in 100 µL volume.

Please see the detailed protocol in the application notes section below. 

Excitation Laser
Red Laser (633 nm)
Application Notes

Apotracker™ Tetra staining procedure for flow cytometry analysis:

  1. To prepare 25 µL (5 tests) of the tetramer solution, mix 5 µL of Apo-monomer, 6 µL of Fluor-Streptavidin and 14 µL of Cell Staining Buffer (BioLegend Cat. No. 420201), or equivalent. 

    Note: We do not recommend preparing less than 25 µL (5 tests) of the Apo-monomer-Streptavidin complex at a time to avoid pipetting errors. Scale up as necessary
     

  2. For each sample containing 1x106 cells resuspended in 100 µL of Cell Staining Buffer, add 5 µL of tetramer solution prepared in the above step.   
     

  3. Incubate in the dark at room temperature for 15 minutes. 
     

  4. Wash each tube by adding 2 mL of Cell Staining Buffer, or equivalent, and centrifuging at 1200 rpm for five minutes. Remove the supernatant and vortex tubes to loosen pellet. 
     

  5. Repeat wash step above. 
     

  6. Resuspend the pellet by adding 300 - 500 μL Cell Staining Buffer to each tube. 
     

  7. (Optional) Ten minutes prior to flow cytometric analysis, add 10 μL of DAPI solution (or equivalent dye) to each tube for viability staining. 
     

  8. Cells are ready for flow cytometric analysis.

Antigen Details

Gene ID
NA
Go To Top Version: 2    Revision Date: 07/28/2023

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

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

BioLegend, the BioLegend logo, and all other trademarks are property of BioLegend, Inc. or their respective owners, and all rights are reserved.

 

8999 BioLegend Way, San Diego, CA 92121 www.biolegend.com
Toll-Free Phone: 1-877-Bio-Legend (246-5343) Phone: (858) 768-5800 Fax: (877) 455-9587

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