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A1si confocal laser microscope

Manufactured by Nikon

The A1si Confocal Laser Microscope is a high-performance imaging system designed for advanced microscopy applications. It utilizes laser technology to provide high-resolution, optical sectioning capabilities for detailed analysis of biological samples.

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4 protocols using a1si confocal laser microscope

1

Nuclear Translocation Analysis of Stress-Induced PMK-1

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L3 animals were mounted in 5 mM sodium azide/M9 buffer on slides with 3% agar pad. pmk-1(re170[pmk-1::mNG^3xFlag]) animals were grown on Comamonas sp. (DA1877) (Avery and Shtonda, 2003 (link)) and mounted in 2 mg/mL tetramisole in M9 buffer on slides with 3% agar pad. We hypothesized that stress caused constitutive translocation to the nucleus. However, growth on Comamonas sp. bacteria, which are thought to be non-inflammatory (Avery and Shtonda, 2003 (link)), did not alter the degree of nuclear translocation. Similarly, mounting animals on tetramisole rather than sodium azide did not abolish nuclear translocation. All images were captured by A1si Confocal Laser Microscope (Nikon) using NIS Elements Advanced Research, Version 4.40 software (Nikon).
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2

Epifluorescent and Confocal Imaging Protocol

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For epifluorescent imaging, animals were mounted in 2 mg/ml tetramisole/M9 buffer and visualized using a Nikon Eclipse TE2000U microscope equipped with a DVC-1412 CCD camera (Digital Video Camera Company), with Hamamatsu SimplePCI acquisition software. Confocal images were captured by A1si Confocal Laser Microscope (Nikon) using NIS Elements Advanced Research, Version 4.40 software (Nikon).
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3

Confocal Imaging of CRISPR-Tagged Strains

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L1 animals were mounted onto slides with a 3% NG agar pad in 5 μL of 2 mg/mL tetramisole/M9 buffer. Confocal images were captured by A1si Confocal Laser Microscope (Nikon) with 488, 561nm lasers using NIS Elements Advanced Research, Version 4.40 software (Nikon). To ensure consistent exposures the same settings were used in imaging of both CRISPR tagged strains: 488nm (115, 0, 5), 561nm (160, 0, 10) (HV, Offset, Laser Power).
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4

Confocal Imaging of CRISPR-tagged Strains

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L1 animals were mounted onto slides with a 3% NG agar pad in 5 µL of 2 mg/mL tetramisole/M9 buffer. Confocal images were captured by A1si Confocal Laser Microscope (Nikon) with 488, 561nm lasers using NIS Elements Advanced Research, Version 4.40 software (Nikon). To ensure consistent exposures the same settings were used in imaging of both CRISPR tagged strains: 488nm (115, 0, 5), 561nm (160, 0, 10) (HV, Offset, Laser Power).
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