Concanavalin A (Con A) Conjugates
Concanavalin A (Con A) Conjugates
Invitrogen™

Concanavalin A (Con A) Conjugates

Thermo Fisher Scientific offers a broad selection of Invitrogen concanavalin A (Con A) conjugates, including Alexa Fluor™ and Alexa Fluor™ Plus conjugates.
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Número de catálogoConjugadoColorExcitación/emisiónSubtipo de proteína
C860TetrametilrodaminaNaranja555/580 nmConcanavalina A (con A)
C11254Alexa Fluor 350Azul346/442 nmConcanavalina A (con A)
C11252Alexa Fluor 488Verde495/519 nmConcanavalina A (con A)
C21401Alexa Fluor 488Verde495/519 nmConcanavalina A, succinilada
C11253Alexa Fluor 594Rojo590/617 nmConcanavalina A (con A)
C21402Alexa Fluor 633Rojo oscuro632/647 nmConcanavalina A (con A)
C21421Alexa Fluor 647Rojo oscuro650/668 nmConcanavalina A (con A)
C56126Alexa Fluor Plus 405Violeta405/450 nmConcanavalina A (con A)
C56127Alexa Fluor Plus 750Infrarrojo cercano750/777 nmConcanavalina A (con A)
C825Texas RedRojo595/615 nmConcanavalina A (con A)
Número de catálogo C860
Precio (MXN)
-
Conjugado:
Tetrametilrodamina
Color:
Naranja
Excitación/emisión:
555/580 nm
Subtipo de proteína:
Concanavalina A (con A)
Thermo Fisher Scientific offers a broad selection of Invitrogen concanavalin A (Con A) conjugates, including Alexa Fluor™ and Alexa Fluor™ Plus conjugates. Concanavalin A (Con A) has been used in a variety of applications, including immunofluorescence (IF), immunohistochemistry (IHC) and flow cytometry (FC). In many cell types, concanavalin A (Con A) is a good marker of ER and Golgi.
Thermo Fisher Scientific offers a broad selection of Invitrogen concanavalin A (Con A) conjugates, including Alexa Fluor and Alexa Fluor Plus conjugates. Concanavalin A selectively binds to alpha‐mannopyranosyl and alpha‐glucopyranosyl residues. In neutral and alkaline solutions, concanavalin A exists as a tetramer with a molecular weight of approximately 104,000 Daltons. In acidic solutions (pH below 5.0), concanavalin A exists as a dimer. Conjugated concanavalin A has been used in variety of applications, including immunofluorescence (IF), immunohistochemistry (IHC), and flow cytometry (FC). 

For Research Use Only. Not for use in diagnostic procedures.
Especificaciones
ColorNaranja
Reactividad cruzadaα-man, α-glc
Excitación/emisión555/580 nm
Sistema de expresiónNatural
Tipo de etiquetaColorantes clásicos
Tipo de ligandoLectin
Familia de proteínasLectins
Subtipo de proteínaConcanavalina A (con A)
Etiqueta de proteínaNone
Grado de pureza o calidadImaging Quality
Cantidad10 mg
Categoría de investigaciónImaging
Condiciones de envíoTemperatura ambiente
FuenteCanavlia ensiformis
ConjugadoTetrametilrodamina
Para utilizar con (aplicación)Immunocytochemistry, Immunohistochemistry, Immunofluorescence
FormularioLyophilized
RecombinanteNative
EspecieC. ensiformis
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de -5 a -30 °C) y proteger de la luz.

Citations & References (56)

Citations & References
Abstract
Effects of the regulatory light chain phosphorylation of myosin II on mitosis and cytokinesis of mammalian cells.
Authors: Komatsu S; Yano T; Shibata M; Tuft R A; Ikebe M;
Journal:J Biol Chem
PubMed ID:10944522
'Myosin plays an important role in mitosis, especially during cytokinesis. Although it has been assumed that phosphorylation of regulatory light chain of myosin (RLC) controls motility of mammalian non-muscle cells, the functional significance of RLC phosphorylation remains uninvestigated. To address this problem, we have produced unphosphorylatable RLC (T18A/S19A RLC) and ... More
Spontaneous and ligand-induced trafficking of CXC-chemokine receptor 4.
Authors:Tarasova NI, Stauber RH, Michejda CJ
Journal:J Biol Chem
PubMed ID:9632631
'A chimeric protein consisting of CXC-chemokine receptor 4 (CXCR4) and the green fluorescent protein (GFP) was used for studying receptor localization and trafficking in real time in stably transduced HeLa, U-937, CEM, and NIH/3T3 cells. CXCR4-GFP was fully active as a co-receptor in mediating human immunodeficiency virus (HIV) entry. Both ... More
Flow cytometric measurement of fluorescence resonance energy transfer on cell surfaces. Quantitative evaluation of the transfer efficiency on a cell-by-cell basis.
Authors:Trón L, Szöllósi J, Damjanovich S, Helliwell SH, Arndt-Jovin DJ, Jovin TM
Journal:Biophys J
PubMed ID:6428482
'A method has been developed for the determination of the efficiency (E) of the fluorescence resonance energy transfer between moieties on cell surfaces by use of a computer-controlled flow cytometer capable of dual wavelength excitation. The absolute value of E may be calculated on a single-cell basis. The analysis requires ... More
Proximity of lectin receptors on the cell surface measured by fluorescence energy transfer in a flow system.
Authors:Chan SS, Arndt-Jovin DJ, Jovin TM
Journal:J Histochem Cytochem
PubMed ID:374620
'Molecules of the lectin concanavalin A have been labeled separately with the fluorescein and rhodamine chromophores and jointly bound to the surface of transformed Friend erythroleukemia cells. The two dyes constitute an ideal donor-acceptor pair for fluorescence resonance energy transfer thereby permitting the determination of the proximity relationships between bound ... More
Immobilization of concanavalin A receptors during differentiation of neuroblastoma cells.
Authors:Fishman MC, Dragsten PR, Spector I
Journal:Nature
PubMed ID:6261153
'Neuroblastoma cells serve as a useful model of neuronal development because compounds such as dimethyl sulphoxide (DMSO) and dibutyryl cyclic AMP cause them to undergo a process of controlled differentiation in tissue culture, during which they can extend long processes, develop characteristic excitability mechanisms, synthesize neurotransmitters and form synapses. We ... More