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Citations & References (12)
Invitrogen™
5-CR 6G, SE (5-Carboxyrhodamine 6G, Succinimidyl Ester), single isomer
5-CR 6G, SE (5-Carboxyrhodamine 6G, Succinimidyl Ester), single isomer
| Catalog Number | Quantity |
|---|---|
| C6127 also known as C-6127 | 5 mg |
Catalog number C6127
also known as C-6127
Price (MXN)
-
Quantity:
5 mg
The amine-reactive form of 5-CR 6G is used for oligonucleotide labeling and automated DNA sequencing applications. Conjugates of this dye have longer-wavelength spectra than the spectra of Lisaamine™ rhodamine B conjugates, but somewhat shorter-wavelength spectra than those of Texas Red™ conjugates.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine
Label or DyeRhodamine 6G
Product Type5-CR 6G 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 (12)
Citations & References
Abstract
Multiplex detection of single-nucleotide variations using molecular beacons.
Journal:Genetic analysis : biomolecular engineering
PubMed ID:10084107
Single-molecule detection of specific nucleic acid sequences in unamplified genomic DNA.
Journal:Anal Chem
PubMed ID:9322430
'A new technique is described for the rapid detection of specific nucleic acid sequences in unamplified DNA samples. The method consists of using two nucleic acid probes complementary to different sites on a target DNA sequence. The two probes are each labeled with different fluorescent dyes. When mixed with a
Wavelength-shifting molecular beacons.
Journal:Nat Biotechnol
PubMed ID:11062440
'We describe wavelength-shifting molecular beacons, which are nucleic acid hybridization probes that fluoresce in a variety of different colors, yet are excited by a common monochromatic light source. The twin functions of absorption of energy from the excitation light and emission of that energy in the form of fluorescent light
Determination of optimal rhodamine fluorophore for in vivo optical imaging.
Journal:Bioconjug Chem
PubMed ID:18610943
'Optical imaging has the potential to improve the efficacy of surgical and endoscopic approaches to cancer treatment; however, the optimal type of fluorescent probe has not yet been established. It is well-known that rhodamine-core-derived fluorophores offer a combination of desirable properties such as good photostability, high extinction coefficient, and high
H-type dimer formation of fluorophores: a mechanism for activatable, in vivo optical molecular imaging.
Journal:ACS Chem Biol
PubMed ID:19480464
'In vivo molecular imaging with target-specific activatable '