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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KatalognummerKonjugatFarbeAnregung/EmissionProtein-Subtyp
C860TetramethylrhodaminOrange555/580 nmConcanavalin A (Con A)
C11254Alexa Fluor 350Blau346/442 nmConcanavalin A (Con A)
C11252Alexa Fluor 488Grün495/519 nmConcanavalin A (Con A)
C21401Alexa Fluor 488Grün495/519 nmConcanavalin A, sukzinyliert
C11253Alexa Fluor 594Rot590/617 nmConcanavalin A (Con A)
C21402Alexa Fluor 633Tiefrot632/647 nmConcanavalin A (Con A)
C21421Alexa Fluor 647Tiefrot650/668 nmConcanavalin A (Con A)
C56126Alexa Fluor Plus 405Lila405/450 nm.Concanavalin A (Con A)
C56127Alexa Fluor Plus 750Nah-Infrarot750/777 nmConcanavalin A (Con A)
C825Texas RedRot595/615 nmConcanavalin A (Con A)
Katalognummer C860
Preis (EUR)
329,65
Exklusiv online
366,00
Ersparnis 36,35 (10%)
Each
Konjugat:
Tetramethylrhodamin
Farbe:
Orange
Anregung/Emission:
555/580 nm
Protein-Subtyp:
Concanavalin A (Con A)
Preis (EUR)
329,65
Exklusiv online
366,00
Ersparnis 36,35 (10%)
Each
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.
Specifications
FarbeOrange
Kreuzreaktivitätα-man, α-glc
Anregung/Emission555/580 nm
ExpressionssystemNatural
MarkertypKlassische Farbstoffe
LigandentypLectin
ProteinfamilieLectins
Protein-SubtypConcanavalin A (Con A)
ProteinmarkierungNone
Reinheits- oder QualitätsgradImaging Quality
Menge10 mg
ForschungskategorieImaging
VersandbedingungRaumtemperatur
QuelleCanavlia ensiformis
KonjugatTetramethylrhodamin
Zur Verwendung mit (Anwendung)Immunocytochemistry, Immunohistochemistry, Immunofluorescence
FormLyophilized
RekombinantNative
SpeziesC. ensiformis
Unit SizeEach
Inhalt und Lagerung
Bei -5 bis -30 °C lagern und vor Licht schützen.

Zitierungen und Referenzen (56)

Zitierungen und Referenzen
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