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Citations & References (25)
Invitrogen™
6-ROX (6-Carboxy-X-Rhodamine), single isomer
6-ROX (6-Carboxy-X-Rhodamine), single isomer
| Catalog Number | Quantity |
|---|---|
| C6156 also known as C-6156 | 10 mg |
Catalog number C6156
also known as C-6156
Price (EUR)
454,00
Each
Quantity:
10 mg
Price (EUR)
454,00
Each
The excitation and emission spectra of carboxyrhodamine 6G (CR 6G) fall between those of fluorescein and tetramethylrhodamine. With a peak absorption at 525 nm, conjugates of carboxyrhodamine 6G are an excellent match to the 514 nm spectral line of the argon-ion laser. The amine-reactive 6-CR 6G, SE can be used to attach this fluorophore to biomolecules of interest including amine-modified oligonucleotides.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine
Emission525
Excitation514
Label or DyeROX
Product Type6-ROX
Quantity10 mg
Reactive MoietyCarboxylic Acid
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
Frequently asked questions (FAQs)
What is the excitation and emission wavelength for rhodamine?
Citations & References (25)
Citations & References
Abstract
Cross-resistance to antifolates in multidrug resistant cell lines with P-glycoprotein or multidrug resistance protein expression.
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
Down-regulation of topoisomerase II by camptothecin does not prevent additive activity of the topoisomerase II inhibitor etoposide in vitro.
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
Evidence for uptake of vital dye by activated rat peritoneal mast cells: an in vitro imaging study.
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
Toxicity of organic fluorophores used in molecular imaging: literature review.
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
Growth inhibition of human glioma cells induced by 8-chloroadenosine, an active metabolite of 8-chloro cyclic adenosine 3':5'-monophosphate.
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