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Citas y referencias (16)
Invitrogen™
BODIPY™ FL (4,4-Difluoro-5,7-Dimethyl-4-Bora-3a,4a-Diaza-s-Indacene-3-Propionic Acid)
BODIPY™ FL (4,4-difluoro-5,7-dimetil-4-bora-3a,4a-diaza-s-indaceno-3-ácido propiónico)
| Número de catálogo | Cantidad |
|---|---|
| D2183 también denominado D-2183 | 5 mg |
Número de catálogo D2183
también denominado D-2183
Precio (MXN)
-
Cantidad:
5 mg
The amine-reactive BODIPY™ FL propionic acid can be used to create green-fluorescent bioconjugates following carbodiimide-activation of the carboxylic acid on the dye and reaction with amines. The electronically neutral BODIPY™ FL dye has the most fluorescein-like spectra of the green-fluorescent BODIPY™ dyes.
El ácido propiónico BODIPY™ FL, es aminorreactivo y se puede utilizar para crear bioconjugados verdes fluorescentes tras la activación de carbodiimida del ácido carboxílico en el colorante y la reacción con aminas. El colorante BODIPY™ FL electrónicamente neutro tiene el espectro más parecido a la fluoresceína de los colorantes BODIPY™ verdes fluorescentes.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Reactividad químicaAmina
Etiqueta o tinteBODIPY™ FL
Tipo de productoÁcido propiónico FL
Cantidad5 mg
Fracción reactivaÁcido carboxílico
Condiciones de envíoTemperatura ambiente
Tipo de etiquetaColorantes BODIPY
Línea de productosBODIPY
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de – 5 a – 30 °C) y proteger de la luz.
Citations & References (16)
Citations & References
Abstract
Thousandfold signal increase using field-amplified sample stacking for on-chip electrophoresis.
Journal:Electrophoresis
PubMed ID:14595694
'Field-amplified sample stacking (FASS) leverages conductivity gradients between a volume of injected sample and the background buffer to increase sample concentration. A major challenge in applying FASS to on-chip assays is the initial setup of high-conductivity gradient boundaries in the region of the injected sample volume. We have designed, fabricated,
Inter- and intramolecular fluorescence quenching of organic dyes by tryptophan.
Journal:Bioconjug Chem
PubMed ID:14624626
'Steady-state and time-resolved fluorescence measurements were performed to elucidate the fluorescence quenching of oxazine, rhodamine, carbocyanine, and bora-diaza-indacene dyes by amino acids. Among the natural amino acids, tryptophan exhibits the most pronounced quenching efficiency. Especially, the red-absorbing dyes ATTO 655, ATTO 680, and the oxazine derivative MR 121 are strongly
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
Interaction of fluorescence labeled single-stranded DNA with hexameric DNA-helicase RepA: a photon and fluorescence correlation spectroscopy study.
Journal:Biochemistry
PubMed ID:11401568
'Fluorescence correlation spectroscopy (FCS) was used to characterize the interaction of fluorescence labeled single-stranded DNA (ssDNA) with hexameric RepA DNA-helicase (hRepA) encoded by plasmid RSF1010. The apparent dissociation constants, Kd(app), for the equilibrium binding of 12mer, 30mer, and 45mer ssDNA 5''-labeled with BFL to hRepA dimer in the presence of
Activation and inhibition of adenylyl cyclase isoforms by forskolin analogs.
Journal:J Pharmacol Exp Ther
PubMed ID:18184830
'Adenylyl cyclase (AC) isoforms 1 to 9 are differentially expressed in tissues and constitute an interesting drug target. ACs 1 to 8 are activated by the diterpene, forskolin (FS). It is unfortunate that there is a paucity of AC isoform-selective activators. To develop such compounds, an understanding of the structure/activity