Alexa Fluor 647

Alexa Fluor 647 is a bright far-red fluorescent dye used to label biological molecules for sensitive detection in medical and biomedical research. It absorbs light near 650 nm and emits fluorescence near 668 nm, allowing instruments to distinguish labeled targets from many sources of background signal and to combine it with other fluorophores. Researchers commonly conjugate Alexa Fluor 647 to antibodies, peptides, or nucleic acid probes for immunofluorescence microscopy, flow cytometry, and fluorescence-based assays. These applications support the identification and measurement of proteins, cells, and tissue features, advancing studies of disease mechanisms, diagnosis, and therapeutic responses.

Alexa Fluor 647 - Related Videos

Research

JoVE Journal - Immunology and Infection

Visualizing Dengue Virus through Alexa Fluor Labeling

0 Views •

Cited by 12 •

2011

Taking advantage of the advancements in fluorophore development and imaging technology, a simple method of Alexa Fluor labeling of dengue virus was devised to visualize the early interactions between virus and cell.

Selective Labelling of Cell-surface Proteins using CyDye DIGE Fluor Minimal Dyes

0 Views •

Cited by 14 •

2008

A simple and specific method was demonstrated for fluorescent labeling and enhanced detection of cell surface proteins without a fractionation step. Differential abundance in cell surface proteins was analyzed using two-dimensional (2-D) electrophoresis and Ettan™ DIGE technology.

Immunofluorescence-Based Visualization of DNA Repair Protein Interactions

0 Views •

2025

In this video, we describe the immunofluorescence method to visualize the localization of the DNA repair proteins γH2AX and 53BP1 at the sites of double-strand DNA breaks in irradiated cell nuclei.

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy (iPALM)

0 Views •

Cited by 10 •

2016

We present a protocol for the application of interferometric PhotoActivated Localization Microscopy (iPALM), a 3-dimensional single-molecule localization super resolution microscopy method, to the imaging of the actin cytoskeleton in adherent mammalian cells. This approach allows light-based visualization of nanoscale structural features that would otherwise remain unresolved by conventional diffraction-limited optical microscopy.

Highly Multiplexed, Super-resolution Imaging of T Cells Using madSTORM

0 Views •

Cited by 4 •

2017

We demonstrate a method to image multiple molecules within heterogeneous nano-structures at single molecule accuracy using sequential binding and elution of fluorescently labeled antibodies.

View All Results

FAQs

Related Topics