Acridine Orange is a cell-permeant nucleic acid binding dye that emits green fluorescence when bound to dsDNA and red fluorescence深入閱讀
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產品號碼
Quantity
A3568
10 mL
產品號碼 A3568
價格 (TWD)
3,930.00
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Ends: 31-Dec-2025
4,900.00
您節省 970.00 (20%)
Each
新增至購物車
Quantity:
10 mL
價格 (TWD)
3,930.00
Online offer
Ends: 31-Dec-2025
4,900.00
您節省 970.00 (20%)
Each
新增至購物車
Acridine Orange is a cell-permeant nucleic acid binding dye that emits green fluorescence when bound to dsDNA and red fluorescence when bound to ssDNA or RNA. This unique characteristic makes acridine orange useful for cell-cycle studies. Acridine orange has also been used as a lysosomal dye.
For Research Use Only. Not for use in diagnostic procedures.
規格
ColorOrange
Detection MethodFluorescence
Dye TypeCell-Permeant
Excitation Wavelength Range460/650 (RNA)
For Use With (Equipment)Fluorescence Microscope
Quantity10 mL
Shipping ConditionRoom Temperature
Label TypeFluorescent Dye
Product TypeDye
SubCellular LocalizationNucleic Acids, Nucleus
Unit SizeEach
內容物與存放
Store in refrigerator 2°C to 8°C and protect from light.
引用資料與參考文獻 (344)
引用資料與參考文獻
Abstract
Low-dose estrogen therapy ameliorates experimental autoimmune encephalomyelitis in two different inbred mouse strains.
Authors:Bebo BF Jr,Fyfe-Johnson A,Adlard K,Beam AG,Vandenbark AA,Offner H
Journal:Journal of immunology (Baltimore, Md. : 1950)
PubMed ID:11160259
Spatial variations in growth rate within Klebsiella pneumoniae colonies and biofilm.
Authors:Wentland EJ,Stewart PS,Huang CT,McFeters GA
Journal:Biotechnology progress
PubMed ID:8652119
The use of acridine orange to visualize and quantify spatial variations in growth rate within Klebsiella pneumoniae colonies and biofilm was investigated. Bacterial colonies supported on polycarbonate filter membranes were grown on R2A agar plates. Some colonies were sampled for cell enumeration, while others were cryoembedded, sectioned, and stained with ... More
Rapid assessment of physiological status in Escherichia coli using fluorescent probes.
Authors:Porter J, Edwards C, Pickup RW
Journal:J Appl Bacteriol
PubMed ID:7592133
'Rapid and direct viability assessment of Escherichia coli in filtered, sterile lake water was possible using multiparameter flow cytometry. Fluorescent dyes were used as probes for different cellular functions (membrane potential, membrane integrity and intracellular enzyme activity), which were correlated with the ability of the cells to respond to nutrient ... More
Defective acidification of intracellular organelles in cystic fibrosis.
Authors:Barasch J, Kiss B, Prince A, Saiman L, Gruenert D, al-Awqati Q
Journal:Nature
PubMed ID:1712081
'The phenotype of cystic fibrosis (CF) includes abnormalities in transepithelial transport of Cl- (refs 1-5), decreased sialylation and increased sulphation and fucosylation of glycoproteins, and lung colonization with Pseudomonas. It is not apparent how these abnormalities are interrelated, nor how they result from loss of function of the CF gene-encoded ... More
Rapid movements of vimentin on microtubule tracks: kinesin-dependent assembly of intermediate filament networks.
Authors:Prahlad V, Yoon M, Moir RD, Vale RD, Goldman RD
Journal:J Cell Biol
PubMed ID:9763428
'The assembly and maintenance of an extended intermediate filament (IF) network in fibroblasts requires microtubule (MT) integrity. Using a green fluorescent protein-vimentin construct, and spreading BHK-21 cells as a model system to study IF-MT interactions, we have discovered a novel mechanism involved in the assembly of the vimentin IF cytoskeleton. ... More