Fibrinogen From Human Plasma, Alexa Fluor™ 488 Conjugate
Fibrinogen From Human Plasma, Alexa Fluor™ 488 Conjugate
Invitrogen™

Fibrinogen From Human Plasma, Alexa Fluor™ 488 Conjugate

Molecular Probes™ fibrinogen conjugates are prepared by attaching fluorescent dye molecules to purified human fibrinogen (approximately 15 dye molecules forRead more
Catalog NumberQuantity
F131915 mg
Catalog number F13191
Price (JPY)
67,500
Each
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Quantity:
5 mg
Molecular Probes™ fibrinogen conjugates are prepared by attaching fluorescent dye molecules to purified human fibrinogen (approximately 15 dye molecules for each fibrinogen molecule), purifying the conjugate to remove unreacted dye, and then lyophilizing for storage.

Fluorescently labeled fibrinogen has proven to be a valuable tool for investigating platelet activation and subsequent fibrinogen binding. For instance, fluorescein-labeled fibrinogen has been used to detect fibrinogen bound to activated platelets by flow cytometry.

Human Fibrinogen Conjugate Specifications:
• Label (Ex/Em): Alexa Fluor™ 488 (∼495/519 nm)
• Spectrally similar to fluorescein, but the signal is less pH-dependent and more photostable
• Lyophilized product can be dissolved in buffer (e.g., sodium bicarbonate, pH 8.3) for use
• Fluorescence is typically detected using fluorescence microscopy or flow cytometry


Find More Probes for Cell Adhesion and Receptor Binding
Review Probes for Cell Adhesion, Chemotaxis, Multidrug Resistance and Glutathione—Section 15.6 and Probes for Following Receptor Binding and Phagocytosis—Section 16.1 in the Molecular Probes™ Handbook for more information on these probes.

For Research Use Only. Not for human or animal therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Label TypeAlexa Fluor Dyes
Product LineAlexa Fluor
Protein SubtypeFibrinogen
Quantity5 mg
Shipping ConditionRoom Temperature
ConjugateAlexa Fluor 488
FormLyophilized
SpeciesHuman
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (17)

Citations & References
Abstract
Assembly of a fibronectin matrix by adherent platelets stimulated by lysophosphatidic acid and other agonists.
Authors:Olorundare OE, Peyruchaud O, Albrecht RM, Mosher DF
Journal:Blood
PubMed ID:11418470
'Lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) are agonists of the endothelial differentiation gene (Edg) family of G-protein-coupled receptors. LPA and S1P are generated by platelet activation during blood coagulation. Both lipids induce assembly of exogenous fibronectin (FN) by fibroblasts. This study examined whether LPA and S1P stimulate binding and assembly ... More
Fibrinogen deposition at the postischemic vessel wall promotes platelet adhesion during ischemia-reperfusion in vivo.
Authors:Massberg S, Enders G, Matos FC, Tomic LI, Leiderer R, Eisenmenger S, Messmer K, Krombach F
Journal:Blood
PubMed ID:10572098
'Following ischemia-reperfusion (I/R), platelet adhesion is thought to represent the initial event leading to remodeling and reocclusion of the vasculature. The mechanisms underlying platelet adhesion to the endothelium have not been completely established. Endothelial cells rendered ischemic acquire a procoagulant phenotype, characterized by fibrinogen accumulation. Therefore, we evaluated whether fibrinogen ... More
Ultrathin self-assembled fibrin sheets.
Authors:O'Brien ET, Falvo MR, Millard D, Eastwood B, Taylor RM, Superfine R,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19052234
'Fibrin polymerizes into the fibrous network that is the major structural component of blood clots and thrombi. We demonstrate that fibrin from three different species can also spontaneously polymerize into extensive, molecularly thin, 2D sheets. Sheet assembly occurs in physiologic buffers on both hydrophobic and hydrophilic surfaces, but is routinely ... More
Reprogramming cell shape with laser nano-patterning.
Authors:Vignaud T, Galland R, Tseng Q, Blanchoin L, Colombelli J, Théry M,
Journal:J Cell Sci
PubMed ID:22357956
Cell shape in vitro can be directed by geometrically defined micropatterned adhesion substrates. However conventional methods are limited by the fixed micropattern design, which cannot recapitulate the dynamic changes of the cell microenvironment. Here, we manipulate the shape of living cells in real time by using a tightly focused pulsed ... More
Kindlin-3 is essential for integrin activation and platelet aggregation.
Authors:Moser M, Nieswandt B, Ussar S, Pozgajova M, Fässler R,
Journal:Nat Med
PubMed ID:18278053
Integrin-mediated platelet adhesion and aggregation are essential for sealing injured blood vessels and preventing blood loss, and excessive platelet aggregation can initiate arterial thrombosis, causing heart attacks and stroke. To ensure that platelets aggregate only at injury sites, integrins on circulating platelets exist in a low-affinity state and shift to ... More