5-CR 6G, SE (5-Carboxyrhodamine 6G, Succinimidyl Ester), single isomer

Citações e referências (12)

Invitrogen™

5-CR 6G, SE (5-Carboxyrhodamine 6G, Succinimidyl Ester), single isomer

Número do catálogo	Quantity
C6127 conhecido também como C-6127	5 mg

Número do catálogo C6127

conhecido também como C-6127

Preço (BRL)

Quantity:

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.

Especificações

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

Conteúdo e armazenamento

Store in freezer (-5 to -30°C) and protect from light.

Citações e referências (12)

Citações e referências

Abstract

Multiplex detection of single-nucleotide variations using molecular beacons.

Authors:Marras SA,Kramer FR,Tyagi S

Journal:Genetic analysis : biomolecular engineering

PubMed ID:10084107

Single-molecule detection of specific nucleic acid sequences in unamplified genomic DNA.

Authors:Castro A, Williams JG

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 ... More

Wavelength-shifting molecular beacons.

Authors:Tyagi S, Marras SA, Kramer FR

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 ... More

Determination of optimal rhodamine fluorophore for in vivo optical imaging.

Authors:Longmire MR, Ogawa M, Hama Y, Kosaka N, Regino CA, Choyke PL, Kobayashi H,

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 ... More

H-type dimer formation of fluorophores: a mechanism for activatable, in vivo optical molecular imaging.

Authors:Ogawa M, Kosaka N, Choyke PL, Kobayashi H,

Journal:ACS Chem Biol

PubMed ID:19480464

'In vivo molecular imaging with target-specific activatable '

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