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Zeiss (Carl Zeiss Microscopy Gmbh) Multiphoton / Zeiss Multiphoton With an AxioImager M1 upright and one AxioObserver inverted microscopes

With an AxioImager M1 upright and one AxioObserver inverted microscopes

Zeiss (Carl Zeiss Microscopy Gmbh) Multiphoton Laser Scanning Confocal Microscope Multiphoton Microscope

Description

Confocal and Multiphoton system with two microscopes:

1) LSM710 with an AxioObserver inverted microscope.

2 fluorescence detectors + 1 Quasar spectral detector + 1 transmission detector

2 Non-descanned detectors

Laser lines: 405/458/488/514/561/633/Infrared MaiTai Deep Sea

Incubation chamber for the microscope

2) LSM510 with an upright AxioImager M1.

1 fluorescence detector + 1 transmission detector 2 Non-descanned detectors Laser lines: 543/Infrared MaiTai Deep Sea

Additional Details

• Objectives
- 5x/0,16 EC "Plan-Neofluar" M27 (Brightfield)

- 10X/0.3 EC Plan-Neofluar M27 (Brightfield)

- 25x/0,8 LCI "Plan-Neofluar" Imm Corr DIC M27 (Oil. Brightfield and DIC II)

- 20X/0.8 Plan-Apochromat (Brightfield and DIC II)

- 40x/1,30 EC "Plan-Neofluar" Oil DIC M27 (Oil. Brightfield and DIC III)

- 63X/1.4 Plan-Apochromat Oil DIC M27 (Oil. Brightfield and DIC III)

- 100x/1,40 Plan-Apochromat" Oil DIC M27 (Oil. Brightfield and DIC III)

- 40x/1,2 Water C-Apochromat" Corr UV-VIS-IR M27 (Water and immersion oil with RI 1.3. Brightfield and DIC III)

- 63x/1.2 Water C-Apochromat Corr UV-VIS-IR M27 (Water and immersion oil with RI 1.3. Brightfield and DIC III)

- 20x/0.5 Water N-Achroplan (Dipping. Brightfield and DIC II)

- 40x/1.0 Water Plan-Apochromat (Dipping. Brightfield and DIC III)

- 63x/1.0 Water Plan-Apochromat (Dipping. Brightfield and DIC III)

• Fluorescence filters
- DAPI/GFP (Ex 395-420/475-500 Em 445-470/510-570) (51000 Chroma)

- CFP/DsRed (Ex 400-440/525-580 Em 460-510/590-710) (55018 Chroma)

• Laser
- Diode 405 nm (on inverted microscope)

- Argon 458/488/514 nm (on inverted microscope)

- HeNe 543nm (on upright microscope)

- DPSS 561 nm (on inverted microscope)

- HeNe 633nm (on inverted microscope)

- MaiTai Deep Sea (Spectra Physics): 690-1020 nm, pulsos inferiores a 100 femtoseg, 2.5 Watt de potencia, 80 Mhz (on both microscopes)

• Confocal filters
“Descanned” detection:

- Inverted microscope with spectral detector: Quasar + 2 PMTs

- Emission wavelenghts: 370-760 nm

- Upright microscope with these filters: BP 390-465, BP 435-485, BP 480-520, BP 500-550, BP 560-615, BP 650-710, KP 660

“Non-Descanned” detection:

- Inverted microscope: BP 380-430, BP 455-500, BP 465-515, BP 500-550, BP 520-560, BP 540-590, BP 565-610

- Upright microscope: BP 440-485, BP 455-500, BP 495-545, BP 500-550, BP 520-560, BP 570-640

• Computer
- Windows Vista in the inverted microscope and XP in the upright one

- Software: Zeiss Zen2010B sp1 in the inverted microscope and Zen 2008 in the upright one



• In Vivo incubation system (Cell Observer-Zeiss) (Inverted microscope)
- Perfusion system

Applicable Technologies

- Live Cell Imaging

Sistema de incubación de PeCon que engloba a casi todo el microscopio con control de temperatura, humedad y pH

- 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...

- Non-Linear Imaging/ Multiphoton fluorescence Imaging

Non-Linear Imaging/ Multiphoton fluorescence Imaging

Multiphoton microscopy uses pulsed long-wavelength light to excite fluorophores within the specimen being observed. The fluorophore absorbs the energy...

- 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...

- 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...

- Photoconversion

Photoconversion

Photoactivatable fluorescent proteins (PAFPs) exhibit fluorescence that can be modified by a light-induced chemical reaction. Many PAFPs have been eng...

- Live Ablation and Pulsed Laser Micro- & Nano-Surgery

Live Ablation and Pulsed Laser Micro- & Nano-Surgery

Laser ablation is a process in which a laser beam is focused on a sample to remove, inactivate, destroy or dissect material within the irradiated zone...