6-ROX (6-Carboxy-X-Rhodamine), single isomer

Zitierungen und Referenzen (25)

Invitrogen™

6-ROX (6-Carboxy-X-Rhodamine), single isomer

6-ROX (6-Carboxy-X-Rhodamin), Einzelisomer

Katalognummer	Menge
C6156 auch als C-6156 bezeichnet	10 mg

Katalognummer C6156

auch als C-6156 bezeichnet

Preis (EUR)

454,00

Menge:

10 mg

Preis (EUR)

454,00

Die Erregungs- und Emissionsspektren von Carboxyrhodamin 6G (CR 6G) liegen zwischen denen von Fluorescein und Tetramethylrhodamin. Mit Absorptionsspitzen bei 525 nm sind die Konjugate von Carboxyrhodamin 6G hervorragend mit der 514 nm-Spektrallinie des Argon-Ionen-Lasers kompatibel. Mit dem aminreaktiven 6-CR 6G, SE kann dieses Fluorophor an Biomoleküle von Interesse, einschließlich aminmodifizierter Oligonukleotide, angebracht werden.

Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.

Specifications

Chemische ReaktivitätAmin

Emission525

Anregung514

Marker oder FarbstoffROX

Produkttyp6-ROX

Menge10 mg

Reaktiver TeilCarbonsäure

VersandbedingungRaumtemperatur

MarkertypKlassische Farbstoffe

Unit SizeEach

Inhalt und Lagerung

Bei -5 bis -30 °C lagern und vor Licht schützen.

Häufig gestellte Fragen (FAQ)

What is the excitation and emission wavelength for rhodamine?

Rhodamine is a generic term for a wide variety of cationic dyes whose fluorescence emission can range from green, orange to red. The table below lists the excitation and emission maxima (nm), as well as molar extinction coefficients (“EC”; cm^-1 M^-1), for various rhodamine dyes (data derived with dye dissolved in methanol).

Dye	Excitation	Emission	EC
Rhodamine B	568	583	88,000
Rhodamine 123	507	529	101,000
Rhodamine 110	499	521	92,000
Rhodamine 6G	528	551	105,000
XRITC	572	596	92,000

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

Zitierungen und Referenzen (25)

Zitierungen und Referenzen

Abstract

Cross-resistance to antifolates in multidrug resistant cell lines with P-glycoprotein or multidrug resistance protein expression.

Authors:van Triest B, Pinedo HM, Telleman F, van der Wilt CL, Jansen G, Peters GJ

Journal:Biochem Pharmacol

PubMed ID:9256160

'Resistance to some (lipophilic) antifolates has been associated with P-glycoprotein (P-gp)-mediated multidrug resistance (MDR). A possible relationship with non-P-gp MDR has not been established. We studied resistance to antifolates in SW-1573 human lung carcinoma cells, a P-gp overexpressing variant SW-1573/2R160 and a multidrug resistance protein (MRP) overexpressing variant SW-1573/2R120. In ... More

Down-regulation of topoisomerase II by camptothecin does not prevent additive activity of the topoisomerase II inhibitor etoposide in vitro.

Authors:Stahl M, Kasimir-Bauer S, Harstrick A

Journal:Anticancer Drugs

PubMed ID:9311443

'Topoisomerases (Topo) I and II are cellular enzymes that catalyze the relaxation of topologically strained DNA and that are involved in a number of DNA-related processes. Their complete inhibition by Topo I and II inhibitors gives promise for improvements in the treatment of malignant diseases. However, preclinical studies showed down-regulation ... More

Evidence for uptake of vital dye by activated rat peritoneal mast cells: an in vitro imaging study.

Authors:Wei JY, Go VL, Taché Y, Kruger L

Journal:Neuroimage

PubMed ID:9343581

'Uptake of material from surrounding medium by activated rat peritoneal mast cells (PMCs) was studied using in vitro peritoneal eluate cells, the vital fluorescent dye sulforhodamine B (SFRM-B), secretagogue compound 48/80, and an imaging technique. PMCs, which undergo different states of degranulation, are shown to possess the ability to take ... More

Toxicity of organic fluorophores used in molecular imaging: literature review.

Authors:Alford R, Simpson HM, Duberman J, Hill GC, Ogawa M, Regino C, Kobayashi H, Choyke PL,

Journal:Mol Imaging

PubMed ID:20003892

'Fluorophores are potentially useful for in vivo cancer diagnosis. Using relatively inexpensive and portable equipment, optical imaging with fluorophores permits real-time detection of cancer. However, fluorophores can be toxic and must be investigated before they can be administered safely to patients. A review of published literature on the toxicity of ... More

Growth inhibition of human glioma cells induced by 8-chloroadenosine, an active metabolite of 8-chloro cyclic adenosine 3':5'-monophosphate.

Authors:Langeveld CH, Jongenelen CA, Heimans JJ, Stoof JC

Journal:Cancer Res

PubMed ID:1617676

'8-Chloroadenosine 3'':5''-monophosphate (8ClcAMP) inhibits the growth of human glioma cell lines at much lower concentrations than more commonly used cyclic AMP analogues, without inducing morphological differentiation. The mechanism by which 8ClcAMP exerts this effect is not fully understood. We examined whether the growth-inhibitory effect of this compound is due to ... More

View all 6-ROX (6-Carboxy-X-Rhodamine), single isomer citations