Vybrant™ Phagocytosis Assay Kit
Vybrant™ Phagocytosis Assay Kit
Invitrogen™

Vybrant™ Phagocytosis Assay Kit

The Vybrant™ Phagocytosis Assay Kit provides a way for researchers to observe and quantitate the process of phagocytosis in humanRead more
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Catalog NumberQuantity
V66941 kit
Catalog number V6694
Price (EUR)
621,65
Online Exclusive
652,00
Save 30,35 (5%)
1 kit
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Add to cart
Quantity:
1 kit
Recurring order eligible. Learn more »
Price (EUR)
621,65
Online Exclusive
652,00
Save 30,35 (5%)
1 kit
Add to cart
Ask our AI about this Product
The Vybrant™ Phagocytosis Assay Kit provides a way for researchers to observe and quantitate the process of phagocytosis in human polynuclear cells and mouse macrophages by following the internalization of a foreign particle—in this case killed E. coli (K-12 strain) cells that have been labeled with the fluorescent dye fluorescein. In addition to the lyophilized E. coli BioParticles™ component, the kit contains a trypan blue solution (to quench the fluorescence from particles that were not internalized) as well as step-by-step instructions for performing this phagocytosis assay in a fluorescence microplate reader. The methodology used with this kit has been developed using an adherent murine macrophage cell line (J774); however, by modifying the cell culture conditions, researchers can adapt this phagocytosis assay to other adherent cell lines.

Vybrant™ Phagocytosis Assay Kit Specifications:
• Particles are fluorescein-labeled E. coli (K-12 strain)
• Kit supplies sufficient reagents for ∼250 tests using 96-well plates
• Fluorescence is measured using a microplate reader (Ex/Em ∼480/520 nm)


Find More BioParticles™ Products
We offer a large range of dye-labeled and unlabeled E. coli (K-12 strain), S. aureus (Wood strain, without protein A), and zymosan (S. cerevisiae) BioParticles™ products. Find out about these products and their applications by reviewing Probes for Following Receptor Binding and Phagocytosis—Section 16.1 in the Molecular Probes™ Handbook.

For pH-sensitive endocytosis assays, see our pHrodo™ BioParticles™ conjugates.

For Research Use Only. Not for human or animal therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Dye TypeClassic Dyes
Format96-well plate
Quantity1 kit
Shipping ConditionRoom Temperature
SpeciesE. coli
For Use With (Equipment)Microplate Reader, Microplate Reader
Product LineVybrant
Product TypePhagocytosis Assay Kit
Unit Size1 kit
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3141825Certificate of AnalysisApr 10, 2025V6694
2860759Certificate of AnalysisMay 30, 2024V6694
2306793Certificate of AnalysisJul 26, 2023V6694
2591247Certificate of AnalysisMar 10, 2023V6694
2539816Certificate of AnalysisSep 26, 2022V6694
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Safety Data Sheets

Frequently asked questions (FAQs)

Phagocytosis is an important mechanism for nourishment in unicellular organisms and for defense against infection in higher vertebrates. The process of phagocytosis can be observed and quantitated in human polynuclear cells and mouse macrophages by following the internalization of a foreign particle such as fluorescently labeled immune complexes and bacterial particles.

We recommend using any medium that is optimal for culturing your cell(s) of interest. Avoid media that have extremes of pH, heavy metals or strong oxidizing/reducing agents as these may degrade the dye fluorescein on the BioParticles and may degrade or precipitate Trypan blue dye.

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

Citations & References (20)

Citations & References
Abstract
Macelignan inhibits melanosome transfer mediated by protease-activated receptor-2 in keratinocytes.
Authors:Choi EJ, Kang YG, Kim J, Hwang JK,
Journal:Biol Pharm Bull
PubMed ID:21532167
'Skin pigmentation is the result of melanosome transfer from melanocytes to keratinocytes. Protease-activated receptor-2 (PAR-2) is a key mediator of melanosome transfer, which occurs as the melanocyte extends its dendrite toward surrounding keratinocytes that take up melanosomes by phagocytosis. We investigated the effects of macelignan isolated from Myristica fragrans HOUTT. ... More
Measurement of growth and viability of cells in culture.
Authors:Patterson MK
Journal:Methods Enzymol
PubMed ID:423756
Induction of C-X-C Chemokine Receptor Type 7 (CXCR7) Switches Stromal Cell-derived Factor-1 (SDF-1) Signaling and Phagocytic Activity in Macrophages Linked to Atherosclerosis.
Authors:Ma W, Liu Y, Ellison N, Shen J,
Journal:J Biol Chem
PubMed ID:23599431
The discovery of CXCR7 as a new receptor for SDF-1 places many previously described SDF-1 functions attributed to CXCR4 in question, though whether CXCR7 acts as a signaling or  ... More
The antimicrobial and phagocytic defense mechanisms of the terrestrial gastropod Lehmannia nyctelia against Escherichia coli and Staphylococcus aureus.
Authors:Lorenson L, DeSantis A, Mannath T, Mirza F, Weeks BS,
Journal:Med Sci Monit
PubMed ID:20980950
Gastropods are significant vectors of human infectious diseases and are exposed to a wide range of soil parasites and micro-organisms. To defend against infection, we hypothesized that the slug produces both soluble and cellular defense mechanisms. In the gastropod Lehmannia nyctelia, soluble antimicrobial activity was measured by disk diffusion assay ... More
Efficient phagocytosis requires triacylglycerol hydrolysis by adipose triglyceride lipase.
Authors:Chandak PG, Radovic B, Aflaki E, Kolb D, Buchebner M, Fröhlich E, Magnes C, Sinner F, Haemmerle G, Zechner R, Tabas I, Levak-Frank S, Kratky D,
Journal:J Biol Chem
PubMed ID:20424161
Macrophage phagocytosis is an essential biological process in host defense and requires large amounts of energy. To date, glucose is believed to represent the prime substrate for ATP production in macrophages. To investigate the relative contribution of free fatty acids (FFAs) in this process, we determined the phagocytosis rates in ... More
20 total citations

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