1x1 image pixel for data collection
LIVE/DEAD™ BacLight™ Bacterial Viability Kits
LIVE/DEAD&trade; <i>Bac</i>Light&trade; Bacterial Viability Kits
Invitrogen™

LIVE/DEAD™ BacLight™ Bacterial Viability Kits

LIVE/DEAD™ BacLight™ Bacterial Viability Kits are easy-to-use fluorescent staining kits commonly used for assessing the viability of bacterial cells. These kits provide a two-color fluorescence assay of bacterial viability using green and red fluorescent dyes for use with imaging, flow, and assays.
Have Questions?
Change viewbuttonViewtableView
Catalog NumberFor Use With (Application)
L7012Microscopy, Quantitative Assays
L13152Viability Assay
L7007Microscopy
Catalog number L7012
Price (USD)
607.65
Online Exclusive
626.00
Save 18.35 (3%)
Each
In stock
Add to cart
For Use With (Application):
Microscopy, Quantitative Assays
Recurring order eligible. Learn more »
Price (USD)
607.65
Online Exclusive
626.00
Save 18.35 (3%)
Each
Add to cart
Ask our AI about this Product

The LIVE/DEAD BacLight Bacterial Viability Kits are convenient and easy-to-use kits for monitoring the viability of bacterial populations based on the membrane integrity of the cell. These kits provide a two-color fluorescence assay of bacterial viability for a diverse array of bacterial genera. Cells with a compromised membrane that are dead or dying will stain red with propidium iodide, whereas cells with an intact membrane will stain green with SYTO™ 9. These kits enable researchers to differentiate between live and dead bacteria within minutes, even in mixed populations with diverse bacterial types through fluorescent imaging, flow cytometry, and microplate assays.

The LIVE/DEAD BacLight Bacterial Viability Kits utilize 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 reduction in the SYTO 9 stain fluorescence when both dyes are present.

The LIVE/DEAD Bac Light Bacterial Viability Kits have been thoroughly tested with a variety of organisms and under several conditions. The kits are ideal for fluorescence microscopy as the live (green fluorescent) and dead (red fluorescent) cells may be viewed separately. They are also suitable for quantitative analysis with a fluorometer, fluorescence microplate reader, flow cytometer, or other instrumentation.

Traditional methods of assessing bacterial viability rely on metabolic characteristics or membrane integrity. However, due to differences in morphology, cytology, and physiology among the many bacterial genera, developing a universally applicable direct-count viability assay has been challenging. The LIVE/DEAD BacLight Bacterial Viability Kits based on membrane integrity allow researchers to distinguish live and dead bacteria easily, reliably, and quantitatively in minutes, even in a mixed population with diverse bacterial types.

The LIVE/DEAD BacLight Bacterial Viability Kit is available in three different formats:

LIVE/DEAD BacLight Bacterial Viability Kit, for microscopy (Cat. No. L7007)
The LIVE/DEAD BacLight Bacterial Viability Kit, for microscopy includes two different premixed solutions of the SYTO 9 and propidium iodide (PI) in 300 μL of DMSO. The fluorescent dyes are mixed at different proportions in each one: Component A – 1.67 mM SYTO 9 & 1.67 mM PI, Component B – 1.67 mM STYO 9 & 18.3 mM PI. This kit is available for customers who have already developed protocols using the premixed dye formulation.

LIVE/DEAD BacLight Bacterial Viability Kit, for microscopy & quantitative assays (Cat. No. L7012)
The LIVE/DEAD BacLight Bacterial Viability Kit, for microscopy & quantitative assays includes two separate solutions of the SYTO 9 (3.34 mM) and propidium iodide (20 mM) dyes in 300 μL of DMSO. The separate staining components enables flexibility for optimization and facilitates the calibration of bacterial fluorescence for quantitative procedures.

LIVE/DEAD BacLight Bacterial Viability Kit (Cat. No. L13152)
For added convenience, the LIVE/DEAD BacLight Bacterial Viability Kit contains 10 pairs of the premeasured separate SYTO 9 and propidium iodide dyes in sealed polyethylene transfer pipets. In addition to the convenient packaging in the sealed pipets, the fluorescent dyes are supplied dry, without DMSO or other solvents. This formulation does not require refrigeration and remains stable at temperatures ≤–20°C once reconstituted.

All three kits come with 10mL of BacLight mounting oil for bacteria immobilized on membranes. The refractive index at 25°C is 1.517 ± 0.003.

Any physiological buffer between pH 7.0–8.0, including PBS, can be used to dilute the SYTO dyes for the staining solution.

At the recommended reagent dilutions and volumes, kits L7007 and L7012 contain sufficient material to perform ≥1000 individual tests in 96-well assay plates, many more tests by fluorescence microscopy or ~200 tests by flow cytometry.

In kit L13152, each applicator pair contains sufficient dye to perform 50 individual tests in a 96-well assay plate, ~1000 assays by fluorescence microscopy or 10 tests by flow cytometry.

The LIVE/DEAD BacLight Bacterial Viability Kits have been tested on the following bacterial species: Bacillus cereus, B. subtilis, Clostridium perfringens, Escherichia coli, Klebsiella pneumoniae, Micrococcus luteus, Mycobacterium phlei, Pseudomonas aeruginosa, P. syringae, Salmonella oranienburg, Serratia marcescens, Shigella sonnei, Staphylococcus aureus and Streptococcus pyogenes. All these bacterial types have shown a good correlation between the results obtained with the LIVE/DEAD BacLight Bacterial Viability Kits and those obtained with standard plate counts.

These tests were performed on logarithmically growing cultures of organisms. In addition, we have received favorable reports from researchers who have used these kits with: Agrobacterium tumefaciens, Edwardsiella ictaluri, Eurioplasma eurilytica, Lactobacillus sp., Mycoplasma hominus, Propionibacterium sp., Proteus mirabilis and Zymomonas sp.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cell TypeBacteria
Detection MethodFluorescence
Dye TypeOther Label(s) or Dye(s)
Quantity1 kit
Shipping ConditionRoom Temperature
For Use With (Application)Microscopy, Quantitative Assays
Product LineBacLight, LIVE/DEAD
Product TypeBacterial Viability Kit
Unit SizeEach
Contents & Storage
Store frozen (-5°C to -25°C) and protect from light.
Have questions about this product? Ask our AI assisted search.
Generating response
This is an AI-powered search and may not always get things right. You can help us make it better with a thumbs up or down on individual answers or by selecting the “Give feedback" button. Your search history and customer login information may be retained by Thermo Fisher and processed in accordance with our Privacy Notice.

Frequently asked questions (FAQs)

When using the LIVE/DEAD BacLight kit for bacterial viability, with SYTO 9 and propidium iodide (PI), why are some cells detected with both dyes? Shouldn't live cells be green and dead cells be red?

SYTO 9 dye will enter all cells, live or dead. PI only enters cells with compromised membranes (dead cells or damaged cells). First, perform single color staining and examine under both filter sets. Longpass filters or the use of too much dye may result in excessive bleedthrough of the green dye emission into the red channel and the emission of PI in the green channel. Use narrower bandpass filters if possible, and use lower concentrations of the dye. Some live cells may take up PI by engulfment; avoid extended incubation times with the dye. Apply PI to a live cell culture and optimize incubation times to limit engulfment.

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

I want to use propidium iodide and SYTO 9 to do LIVE/DEAD testing of a bacterial sample. Will anaerobic conditions adversely affect the assay?

Oxygen content should not affect the binding of propidium iodide and SYTO 9 to nucleic acids. SYTO 9 will label all cells, and propidium iodide will label only dead cells or cells with a compromised membrane.

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

I have a LIVE/DEAD BacLight Bacterial Viability kit that has SYTO 9 and propidium iodide in it. Will I be able to stain eukaryotic cells that have engulfed bacteria and determine if the bacteria are alive or dead using this kit?

Unfortunately, no. SYTO 9 will label the nuclei of live or dead cells, including the eukaryotic cells. Propidium iodide is cell impermeant, and will only enter dead cells. If the eukaryotic cells are dead, they will label with propidium iodide as well. If the eukaryotic cells are alive, propidium iodide will not be able to enter and thus will not label the bacteria inside, whether the bacteria are alive or dead. We are not aware of any way to do a viability assay of bacteria once they have been engulfed by cells.

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

Do you offer the propidium iodide (20 mM) dyes in 300 µL of DMSO, that are part of the LIVE/DEAD™ BacLight™ Bacterial Viability Kits (Cat. No. L7012), as a standalone product?

We do not offer the propidium iodide as a standalone, packaged the same way.

We do offer 100 mg of powder Propidium Iodide (Cat. No. P1304MP). This product can be used to make a stock at your desired concentration.
We also offer Propidium Iodide - 1.0 mg/mL Solution in Water (Cat. No. P3566), which is packaged as 10 mL of a 1 mg/ml (= 1.5 mM) stock solution in water.
We recommend running a concentration titration with control cells first, before using these products for labeling bacteria.

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

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.

Figures

Fluorescence spectra

Fluorescence spectra

Customers who viewed this item also viewed



Documents & Downloads

Certificates

Lot #Certificate TypeDateCatalog Number(s)
3148293Certificate of AnalysisMay 18, 2025L7012
3143931Certificate of AnalysisApr 10, 2025L13152
3101973Certificate of AnalysisJan 07, 2025L7007
3011783Certificate of AnalysisNov 07, 2024L13152
3006769Certificate of AnalysisOct 11, 2024L7012
5 results displayed, search above for a specific certificate

Safety Data Sheets

Citations & References (172)

Citations & References
Abstract
Authors:
Journal:
PubMed ID:16517648
Real-time PCR analysis of Vibrio vulnificus from oysters.
Authors:Campbell MS, Wright AC
Journal:Appl Environ Microbiol
PubMed ID:14660359
Vibrio vulnificus is an opportunistic human pathogen commonly found in estuarine environments. Infections are associated with raw oyster consumption and can produce rapidly fatal septicemia in susceptible individuals. Standard enumeration of this organism in shellfish or seawater is laborious and inaccurate; therefore, more efficient assays are needed. An oligonucleotide probe ... More
Ethidium monoazide for DNA-based differentiation of viable and dead bacteria by 5'-nuclease PCR.
Authors:Nogva HK, Drømtorp SM, Nissen H, Rudi K
Journal:Biotechniques
PubMed ID:12703305
'PCR techniques have significantly improved the detection and identification of bacterial pathogens. Even so, the lack of differentiation between DNA from viable and dead cells is one of the major challenges for diagnostic DNA-based methods. Certain nucleic acid-binding dyes can selectively enter dead bacteria and subsequently be covalently linked to ... More
Escherichia coli cells with increased levels of DnaA and deficient in recombinational repair have decreased viability.
Authors:Grigorian AV, Lustig RB, Guzmán EC, Mahaffy JM, Zyskind JW
Journal:J Bacteriol
PubMed ID:12511510
'The dnaA operon of Escherichia coli contains the genes dnaA, dnaN, and recF encoding DnaA, beta clamp of DNA polymerase III holoenzyme, and RecF. When the DnaA concentration is raised, an increase in the number of DNA replication initiation events but a reduction in replication fork velocity occurs. Because DnaA ... More
Substratum topography influences susceptibility of Salmonella enteritidis biofilms to trisodium phosphate.
Authors:Korber DR, Choi A, Wolfaardt GM, Ingham SC, Caldwell DE
Journal:Appl Environ Microbiol
PubMed ID:9292984
'Established (48- and 72-h) Salmonella enteritidis biofilms grown in glass flow cells with or without artificial crevices (0.5-, 0.3-, and 0.15-mm widths) were subjected to a 10% trisodium phosphate (TSP) solution under different flow regimens (0.3, 0.6, 1.2, and 1.8 cm s-1). The abundance of biofilm remaining after TSP treatment, ... More
172 total citations

Other products to consider



Share catalog number, name or link

1x1 image pixel for data collection