Filmtracer™ LIVE/DEAD™ Biofilm Viability Kit
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Filmtracer™ LIVE/DEAD™ Biofilm Viability Kit
Invitrogen™

Filmtracer™ LIVE/DEAD™ Biofilm Viability Kit

The FilmTracer™ LIVE⁄DEAD Biofilm Viability kit provides a two-color fluorescence assay of bacterial viability, based on membrane integrity, that hasRead more
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Catalog NumberQuantity
L103161 kit
Catalog number L10316
Price (CNY)
5,703.00
飞享价
Ends: 31-Dec-2025
7,730.00
Save 2,027.00 (26%)
Each
Add to cart
Quantity:
1 kit
Price (CNY)
5,703.00
飞享价
Ends: 31-Dec-2025
7,730.00
Save 2,027.00 (26%)
Each
Add to cart
The FilmTracer™ LIVE⁄DEAD Biofilm Viability kit provides a two-color fluorescence assay of bacterial viability, based on membrane integrity, that has proven usefule for a diverse array of bacterial genera including those growing in biofilm communities. The LIVE⁄DEAD Biofilm Viability kit utilizes mixtures of our SYTO® 9 green fluorescent nucleic acid stain and the red-fluorescent nucleic acid stain, propidium iodide. These stains differ both in their spectral characteristics and in their ability to penetrate healthy bacterial cells. When used alone, the SYTO® 9 stain generally labels all bacteria in a population—those with intact membranes and those with damaged membranes. In contrast, propidium iodide penetrates only bacteria with damaged membranes, causing a rduction in the SYTO® 9 stain fluorescence with both dyes are present. Thus, with an appropriate mixture of the SYTO™ 9 and propdium iodide stains, bacteria with intact cell membranes stain fluorescent green, whereas bacteria with damaged membranes stain fluorescent red.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Dye TypeSYTO™ 9, propidium iodide
FormLiquid
Quantity1 kit
Shipping ConditionRoom Temperature
Sub Cellular LocalizationCytoplasm & Cytosol
ColorRed, Green
EmissionVisible
For Use With (Application)Viability Assay
For Use With (Equipment)Confocal Microscope, Fluorescence Microscope, Flow Cytometer, Microplate Reader, Fluorescent Imager
Product LineFilmTracer, Molecular Probes
Product TypeBiofilm Viability Kit
Unit SizeEach
Contents & Storage
2 ingredients, store in freezer -5°C to -30°C; protect from light

Frequently asked questions (FAQs)

How do I prepare dead cell controls for LIVE/DEAD cell viability assays?

There are two easy options. One is to heat-inactivate the cells by placing at 60 degrees C for 20 minutes. The second is to subject the cells to 70% ethanol. Alcohol-fixed cells can be stored indefinitely in the freezer until use, potentially up to several years.

Centrifuge cells, pellet, and remove supernatant.
Fix cells: Add 10 mL ice cold 70% ETOH to a 15 mL tube containing the cell pellet, adding dropwise at first while vortexing, mix well.
Store in freezer until use.
When ready to use, wash twice and resuspend in buffer of choice.

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

Citations & References (14)

Citations & References
Abstract
Biofilm formations in nasopharyngeal tissues of patients with nasopharyngeal osteoradionecrosis.
Authors:Tsai YJ, Lin YC, Wu WB, Chiu PH, Lin BJ, Hao SP,
Journal:Otolaryngol Head Neck Surg
PubMed ID:23348872
'Objective Determine the presence of nasopharynx biofilms in patients with nasopharyngeal cancer (NPC) and osteoradionecrosis (ORN) and patients with NPC but no ORN. Study Design Cross-sectional study. Setting Tertiary referral medical center. Subjects and Methods We enrolled 27 patients with NPC from our outpatient clinic during January 2010 to June ... More
Comparison of methods for evaluation of the bactericidal activity of copper-sputtered surfaces against methicillin-resistant Staphylococcus aureus.
Authors:Rio L, Kusiak-Nejman E, Kiwi J, Bétrisey B, Pulgarin C, Trampuz A, Bizzini A,
Journal:Appl Environ Microbiol
PubMed ID:22983970
Bacteria can survive on hospital textiles and surfaces, from which they can be disseminated, representing a source of health care-associated infections (HCAIs). Surfaces containing copper (Cu), which is known for its bactericidal properties, could be an efficient way to lower the burden of potential pathogens. The antimicrobial activity of Cu-sputtered ... More
Fratricide is essential for efficient gene transfer between pneumococci in biofilms.
Authors:Wei H, Håvarstein LS,
Journal:Appl Environ Microbiol
PubMed ID:22706053
Streptococcus pneumoniae and a number of commensal streptococcal species are competent for natural genetic transformation. The natural habitat of these bacteria is multispecies biofilms in the human oral cavity and nasopharynx. Studies investigating lateral transfer of virulence and antibiotic resistance determinants among streptococci have shown that interspecies as well as ... More
Comparison of different live/dead stainings for detection and quantification of adherent microorganisms in the initial oral biofilm.
Authors:Tawakoli PN, Al-Ahmad A, Hoth-Hannig W, Hannig M, Hannig C,
Journal:Clin Oral Investig
PubMed ID:22821430
The aim of the present study was to investigate different fluorescence-based, two-color viability assays for visualization and quantification of initial bacterial adherence and to establish reliable alternatives to the ethidium bromide staining procedure. Bacterial colonization was attained in situ on bovine enamel slabs (n?=?6 subjects). Five different live/dead assays were ... More
Rapid Bacterial Detection during Endodontic Treatment.
Authors:
Journal:J Dent Res
PubMed ID:28530469