Acridin Orange ist ein membrangängiger Nukleinsäure bindender Farbstoff, der bei Bindung an dsDNA grüne Fluoreszenz und bei Bindung an ssDNAWeitere Informationen
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Katalognummer
Menge
A3568
10 ml
Katalognummer A3568
Preis (EUR)
170,00
Each
Menge:
10 ml
Preis (EUR)
170,00
Each
Acridin Orange ist ein membrangängiger Nukleinsäure bindender Farbstoff, der bei Bindung an dsDNA grüne Fluoreszenz und bei Bindung an ssDNA oder RNA rote Fluoreszenz aussendet. Diese einzigartige Eigenschaft macht Acridin Orange für Zellzyklus-Studien nützlich. Acridin Orange wurde auch als lysosomaler Farbstoff verwendet.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
FarbeOrange
NachweisverfahrenFluoreszent
FarbstofftypMembrangängig
Anregungswellenlängenbereich460/650 (RNA)
Zur Verwendung mit (Geräte)Fluoreszenzmikroskop
Menge10 ml
VersandbedingungRaumtemperatur
MarkertypFluorescent Dye
ProdukttypFarbstoff
Sub Cellular LocalizationZellkern, Nukleinsäuren, Nucleus
Unit SizeEach
Inhalt und Lagerung
Im Kühlschrank (2–8 °C) aufbewahren und vor Licht schützen.
Zitierungen und Referenzen (344)
Zitierungen und Referenzen
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