Alexa fluor 488

In aqueous mounting media they are brighter than FITC, Cy and DyLight 488. Ideal for multi-color analysis. Cited in 1publications.

It has an excitation maximum at 4nm . Find MSDS or SDS, a COA, data sheets and more information.

Detection of Axl in HeLa Human Cell Line by Flow Cytometry. Your browsing activity is empty. Activity recording is turned off. Support Center Support Center. CST – Customer satisfaction is our highest priority.

Backed by our 1 Guarantee. Definition, A fluorescent dye of absorption wavelength 4nm and emission wavelength 5nm, derived from a 6-diaminoxanthenium-5-disulfate.

Alexa Fluor 4- Molecular Imaging and Contrast Agent Database (MICAD). Our antibodies are available across human, mouse, and rat catalog ranges. Furthermore, the dye has been encapsulated into a polymer nanosphere by a microemulsion metho producing 1nm part. Streptavidin has a very high binding affinity for biotin, and a conjugate of streptavidin is commonly used together with a conjugate of biotin for specific detection of a variety of proteins, . Monoclonal Antibody for studying Vimentin in the Cytoskeletal Signaling research area. Designed by TriLink Aerospace Marketing Inc.

Reproduced with the constant, will be nearer to that of . This set replaces XF421. Immunohistochemistry (frozen sections) Immunofluorescence Immunohistochemistry (Paraffin-embedded Sections) ELISA Flow Cytometry Western Blot Immunoprecipitation Immunocytochemistry Immunohistochemistry ( IHC) Bio Assay. Bioss Antibodies is dedicated to developing and manufacturing top quality antibodies that accelerate biological research and discovery. Enables easy, fast labeling of primary antibodies or proteins with ALEXA Fluor 488.

Both Erkand Erk(pand pMAP kinases) function in a protein kinase cascade that plays a critical role in the regulation of cell growth and differentiation. MAP kinases are activated by a wide variety of extracellular signals including growth and neurotrophic factors, . Endothelial cell (EC) migration is a critical event during multiple physiological and pathological processes. ECs move in the plane of the endothelium to heal superficially injured blood vessels but migrate in three dimensions during angiogenesis.

We herein investigate differences in these modes of movement focusing on .