The largest database of trusted experimental protocols

Lsm880 airyscan fcs confocal microscope system

Manufactured by Zeiss

The LSM880 Airyscan/FCS confocal microscope system is a high-resolution imaging solution designed for advanced microscopy applications. It features the Airyscan detection technology, which provides improved signal-to-noise ratio and increased resolution. The system also includes Fluorescence Correlation Spectroscopy (FCS) capabilities for analyzing molecular dynamics and interactions.

Automatically generated - may contain errors

2 protocols using lsm880 airyscan fcs confocal microscope system

1

FCCS Imaging of Subcellular Dynamics

Check if the same lab product or an alternative is used in the 5 most similar protocols
Primary ear fibroblast cells were plated in fibronectin-coated glass-bottom μ-Slide 8 Well high chambered coverslip (ibidi). 24 h after cell plating, the samples were taken for FCCS experiment. Two-color FCCS experiments were performed for both nuclear and cytoplasmic compartments in each cell. Each FCCS experiment was performed for 10 s with 3 technical repeats on the same spot. The experiments were performed using Zeiss LSM880 Airyscan/FCS confocal microscope system with environmental control. The mEGFP was excited with the 488-nm Argon laser line and the mScarlet was excited with the 561-nm DPSS laser line. The C-Apochromat, 40x, 1.2 NA water-immersion objective was used for all the experiments. The emission signal was split by a dichroic mirror MBS 488/561/633 and detected at 505–530 nm for mEGFP and 570–600 nm for mScarlet using the GaAsP PMT array detector. The confocal pinhole was set for 1.0 airy unit (approximately 0.8756 and 1.33 fL for 488 nm and 561 nm) for both channels calibrated in the x-y plane for maximum signal intensity.
+ Open protocol
+ Expand
2

FCCS Imaging of Subcellular Dynamics

Check if the same lab product or an alternative is used in the 5 most similar protocols
Primary ear fibroblast cells were plated in fibronectin-coated glass-bottom μ-Slide 8 Well high chambered coverslip (ibidi). 24 h after cell plating, the samples were taken for FCCS experiment. Two-color FCCS experiments were performed for both nuclear and cytoplasmic compartments in each cell. Each FCCS experiment was performed for 10 s with 3 technical repeats on the same spot. The experiments were performed using Zeiss LSM880 Airyscan/FCS confocal microscope system with environmental control. The mEGFP was excited with the 488-nm Argon laser line and the mScarlet was excited with the 561-nm DPSS laser line. The C-Apochromat, 40x, 1.2 NA water-immersion objective was used for all the experiments. The emission signal was split by a dichroic mirror MBS 488/561/633 and detected at 505–530 nm for mEGFP and 570–600 nm for mScarlet using the GaAsP PMT array detector. The confocal pinhole was set for 1.0 airy unit (approximately 0.8756 and 1.33 fL for 488 nm and 561 nm) for both channels calibrated in the x-y plane for maximum signal intensity.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!