Description
Microscopio Láser Confocal invertido con 5 líneas de láser de excitación: Diodo (405 nm), Argón (458, 488, 514 nm), HeNe (543 nm), HeNe (594 nm) y HeNe (633 nm), objetivos 10x, 20x (en seco), 40x, 63x (inmersión en aceite) y 63x (inmersión en agua y glicerol), técnicas de luz transmitida (campo claro y DIC), filtros (DAPI, GFP y DsRed), con 3 canales de detección internos o fotomultiplicadores (PMTs), completamente motorizado y sistema de incubación con control de CO2 y temperatura para realizar ensayos “in vivo”.
Applicable Technologies
- Laser Scanning Confocal Microscopy
Laser Scanning Confocal Microscopy
Confocal microscopy offers several advantages over conventional widefield optical microscopy, including the ability to control depth of field, elimina...
- Live Cell Imaging
Live Cell Imaging
Cell biologists are increasingly using live-cell imaging techniques to provide clues into the fundamental nature of cellular and tissue structure and...
- Photobleaching Techniques/ FRAP-Fluorescence Recovery After Photoble...
Photobleaching Techniques/ FRAP-Fluorescence Recovery After...
Photobleaching techniques are used as a strategy to reveal the diffusion/binding dynamics of molecules or the exchange between compartments in live ce...
- FRET- Förster Resonance Energy Transfer
FRET- Förster Resonance Energy Transfer
Förster Resonance Energy Transfer (FRET) is a process where an excited fluorophore (donor)transfers energy to another fluorophore (acceptor) [1]. Reso...
- Photobleaching Techniques/ FLIP-Fluorescence Loss In Photobleaching
Photobleaching Techniques/ FLIP-Fluorescence Loss In Photobl...
This technique is used to study the diffusion of molecules among different connected/communicated cell compartments. A fluorescent cell is repeatedly...
- Photoactivation PA-FPs
Photoactivation PA-FPs
Photoactivatable fluorescent proteins (PAFPs) exhibit fluorescence that can be modified by a light-induced chemical reaction. Many PAFPs have been eng...