Filmtracer™ LIVE/DEAD™ 生物膜细胞活力检测试剂盒
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Filmtracer™ LIVE/DEAD™ 生物膜细胞活力检测试剂盒
Invitrogen™

Filmtracer™ LIVE/DEAD™ 生物膜细胞活力检测试剂盒

The FilmTracer™ LIVE⁄DEAD Biofilm Viability kit provides a two-color fluorescence assay of bacterial viability, based on membrane integrity, that has了解更多信息
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货号数量
L103161 kit
货号 L10316
价格(CNY)
5,703.00
飞享价
Ends: 31-Dec-2025
7,730.00
共减 2,027.00 (26%)
Each
添加至购物车
数量:
1 kit
价格(CNY)
5,703.00
飞享价
Ends: 31-Dec-2025
7,730.00
共减 2,027.00 (26%)
Each
添加至购物车
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.
仅供科研使用。不可用于诊断程序。
规格
检测方法荧光
染料类型SYTO™ 9、碘化丙啶
形式液体
数量1 kit
运输条件室温
子细胞定位细胞质&细胞液
颜色红色,绿色
发射可见光
适用于(应用)活力测定试剂盒
适用于(设备)共聚焦显微镜, 荧光显微镜, 流式细胞仪, 微孔板读数仪, 荧光成像仪
产品线FilmTracer、Molecular Probes
产品类型生物膜活力试剂盒
Unit SizeEach
内容与储存
2种组分,冷冻储存(-5°C 至 -30°C);避光

常见问题解答 (FAQ)

我如何为LIVE/DEAD细胞活力实验准备死细胞对照?

有两种简单的方法。一种是通过60°C放置20分钟热灭活细胞。第二种是将细胞放入70%乙醇。乙醇固定的细胞可以在冰箱中无限期储存直到使用,可达好几年。

1.离心细胞、使细胞沉淀并去除上清
2.固定细胞:在15mL含有细胞团的试管中加入10 mL70%冰乙醇,先开始逐滴加入后震荡,混合均匀。
3.在冰箱中储存直到使用。
4.快使用时,水洗两次且在选择的缓冲液中重悬。

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.

引用和文献 (14)

引用和文献
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