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Citations & References (48)
Invitrogen™
5-ROX, SE (5-Carboxy-X-Rhodamine, Succinimidyl Ester), single isomer
5-ROX, SE (5-Carboxy-X-Rhodamine, Succinimidyl Ester), single isomer
| Catalog Number | Quantity |
|---|---|
| C6125 | 5 mg |
Catalog number C6125
Price (MXN)
-
Quantity:
5 mg
The isomeric 5-ROX, SE is an amine-reactive form of carboxy-X-rhodamine and is widely used for oligonucleotide labeling and automated DNA sequencing applications.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine
Label or DyeROX
Product Type5-ROX SE
Quantity5 mg
Reactive MoietyActive Ester, Succinimidyl Ester
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
Citations & References (48)
Citations & References
Abstract
Real-time, sequence-specific detection of nucleic acids during strand displacement amplification.
Journal:Analytical biochemistry
PubMed ID:10603241
The engineering of membrane-permeable peptides.
Journal:Analytical biochemistry
PubMed ID:15907875
Molecular beacons: a new approach for semiautomated mutation analysis.
Journal:Clin Chem
PubMed ID:9510851
Molecular beacons are oligonucleotide probes that become fluorescent upon hybridization. We designed molecular beacons to detect a point mutation in the methylenetetrahydrofolate reductase (MTHFR) gene, a mutation that has been related to an increased risk for cardiovascular disease and neural tube defects. The application of molecular beacons enables fast, semiautomated,
Sites of tubulin polymerization in PC12 cells.
Journal:J Neurochem
PubMed ID:2179472
'The site at which tubulin enters into polymer in the neuritic process is a very important datum in terms of our understanding of the mechanism of transport of the microtubular cytoskeleton out the axon. If the form of tubulin being transported out the axon is the microtubule, then assembly of
Kinetic studies by fluorescence resonance energy transfer employing a double-labeled oligonucleotide: hybridization to the oligonucleotide complement and to single-stranded DNA.
Journal:Biochemistry
PubMed ID:7819209
'A single 16-base oligodeoxyribonucleotide was labeled at the 3''-end with fluorescein and at the 5''-end with x-rhodamine (R*oligo*F); the chromophores served as a donor/acceptor pair, respectively, for Förster resonance energy transfer. We exploited the striking differences in the steady-state emission spectra of the R*oligo*F as a single strand and in