pHrodo™ Red Phagocytosis Particle Labeling Kit for Flow Cytometry
pHrodo™ Red Phagocytosis Particle Labeling Kit for Flow Cytometry
Invitrogen™

pHrodo™ Red Phagocytosis Particle Labeling Kit for Flow Cytometry

• Specifically detect phagocytosis and endocytosis with pH-sensitive fluorogenic dye - discriminate endcytosed from adherent and extracellular particles• Reduced signal자세히 알아보기
Have Questions?
카탈로그 번호수량
A100261 kit
카탈로그 번호 A10026
제품 가격(KRW)
1,772,000
온라인 행사
Ends: 31-Dec-2025
2,084,000
할인액 312,000 (15%)
Each
카트에 추가하기
수량:
1 kit
제품 가격(KRW)
1,772,000
온라인 행사
Ends: 31-Dec-2025
2,084,000
할인액 312,000 (15%)
Each
카트에 추가하기
• Specifically detect phagocytosis and endocytosis with pH-sensitive fluorogenic dye - discriminate endcytosed from adherent and extracellular particles
• Reduced signal variability and improved timing in sensitive experiments - no need for wash steps or quencher dye
• Bright red fluorescence - conveniently multiplex with green dyes such as GFP, Fluo-4, or calcein

View a selection guide for all pHrodo Indicators used in imaging, flow cytometry and microplate assays.

The pHrodo™ Red dye gives faster and more accurate results than any other phagocytosis assay

The new Molecular Probes™ proprietary pH-sensitive rhodamine-based pHrodo™ Red dye is non-fluorescent at neutral pH, but turns bright red upon acidification. Because it is both fluorogenic and pH-sensitive, the pHrodo™ Red dye can be used as a specific sensor of phagocytic events; acidification of the phagosome following phagocytosis is marked by red fluorescence. It is therefore an ideal tool with which to study phagocytosis and its regulation by drugs and/or environmental factors.

Rapid and reproducible

Wash steps and quencher dyes are not needed since the pHrodo™ Red dye is non-fluorescent outside the cell, making the staining protocol simple and fast. The elimination of wash steps and quencher dyes also improves assay reproducibility, particularly in plate reader-based assays.

Flexible applications

Use ready-made pHrodo™ Red BioParticles™ conjugates for convenient analysis of phagocytosis of Gram-positive or Gram-negative bacteria, or the amine-reactive pHrodo™ Red SE form for labeling microorganisms or proteins of your choice.

Compatible with multiple platforms
pHrodo™ Red dye conjugates can be used in plate readers, fluorescence microscopy imaging, and flow cytometry applications. The pHrodo™ Red Phagocytosis Particle Labeling Kit and the pHrodo™ Red E. coli BioParticles™ Phagocytosis Kit for flow cytometry were designed for rapid and convenient measurements of phagocytic activity in whole blood samples by flow cytometry. The kits include all the reagents required for assessing particle ingestion and red blood cell lysis. The Labeling Kit also contains the reagents required for labeling microorganisms with the pHrodo™ Red dye. Sufficient reagents are provided in both kits for approximately 100 assays.

The optimal absorption and fluorescence emission maxima of the pHrodo™ Red BioParticles™ conjugate is approximately 560 nm and 585 nm, respectively. However, the fluorophore is readily excited with the 488 nm argon-ion laser installed on most flow cytometers.
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
염료 유형pHrodo™ Red
형식Bottle(s)
수량1 kit
배송 조건Room Temperature
Emission560/585
용도 (장비)Flow Cytometer
제품라인pHrodo
제품 유형Red Phagocytosis Particle Labeling Kit
Unit SizeEach
구성 및 보관
Contains lysis buffer (10 mL), buffer B (200 mL), wash buffer (200 mL), 1 vial pHrodo™ red succinimidyl ester (1 mg, lyophilized product), 1 vial DMSO (0.5 mL), 1 bottle sodium bicarbonate (50 mL, 0.1 M, pH 9.3). Store in refrigerator

자주 묻는 질문(FAQ)

I am performing a phagocytosis assay of macrophages engulfing pHrodo-labeled bacteria. What do you recommend for fixation after the phagocytosis?

pHrodo is relatively non-fluorescent until it enters the acidic phagosome, at which point its fluorescence increases. If you fix the sample, the pHrodo will only reflect the pH of the buffer the cells are in, and not the pH of the phagosome. For this reason, we do not recommend fixing samples. If you want to see how many cells engulfed the labeled bacteria, fix the cells and then place the fixed cells in an acidic buffer for the assay.

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

인용 및 참조 문헌 (3)

인용 및 참조 문헌
Abstract
SLAM is a microbial sensor that regulates bacterial phagosome functions in macrophages.
Authors:Berger SB, Romero X, Ma C, Wang G, Faubion WA, Liao G, Compeer E, Keszei M, Rameh L, Wang N, Boes M, Regueiro JR, Reinecker HC, Terhorst C,
Journal:Nat Immunol
PubMed ID:20818396
'Phagocytosis is a pivotal process by which macrophages eliminate microorganisms after recognition by pathogen sensors. Here we unexpectedly found that the self ligand and cell surface receptor SLAM functioned not only as a costimulatory molecule but also as a microbial sensor that controlled the killing of gram-negative bacteria by macrophages. ... More
Ehrlichia chaffeensis infections in Drosophila melanogaster.
Authors:Luce-Fedrow A, Von Ohlen T, Chapes SK,
Journal:Infect Immun
PubMed ID:19687202
Ehrlichia chaffeensis is an obligate, intracellular bacterium, transmitted by the tick Amblyomma americanum, and is the causative agent of human monocytic ehrlichiosis infections. We previously demonstrated that E. chaffeensis is capable of growing in Drosophila S2 cells. Therefore, we tested the hypothesis that E. chaffeensis can infect adult Drosophila melanogaster. ... More
Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing.
Authors:Meena NP, Kimmel AR
Journal:Elife
PubMed ID:28541182
Aspects of innate immunity derive from characteristics inherent to phagocytes, including chemotaxis toward and engulfment of unicellular organisms or cell debris. Ligand chemotaxis has been biochemically investigated using mammalian and model systems, but precision of chemotaxis towards ligands being actively secreted by live bacteria is not well studied, nor has ... More