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Lumen 200 w metal arc lamp

Manufactured by Prior Scientific
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The Lumen 200-W metal arc lamp is a high-intensity light source that generates illumination through the use of a metal arc. It provides a stable and consistent light output for various laboratory applications.

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Lab products found in correlation

Eclipse ti u inverted microscope, by Nikon (3 mentions) Plan apo 100 1.49 n a oil, by Nikon (2 mentions) Fiber launch tirfm, by Nikon (2 mentions)

Close spelling variants of this product

Lumen 200 metal arc lamp Lumen 200

3 protocols using lumen 200 w metal arc lamp

1

Single Molecule Filament Sliding Assay

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
All filament sliding assays were performed at room temperature (22 ± 1°C) using a Nikon Eclipse Ti-U inverted microscope equipped with a Plan Apo 100X 1.49 N.A. oil emersion lens for through-the-objective total internal reflection microscopy (TIRFM) or epifluorescence microscopy as described (8 (link), 9 (link)). Briefly, either a 532-nm diode-pumped, solid-state, 50-mW laser (Lasever Inc.) or Lumen 200-W metal arc lamp (Prior Scientific) were used for excitation. Images were collected using an intensified high-resolution XR/Turbo-Z, 10-bit digital camera (Stanford Photonics).
O’Lea ry T.S., Snyder J., Sadayappan S., Day S.M, & Previs M.J. (2018). MYBPC3 truncation mutations enhance actomyosin contractile mechanics in human hypertrophic cardiomyopathy. Journal of molecular and cellular cardiology, 127, 165-173.
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2

Thin Filament Sliding Assay Protocol

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All native thin filament sliding assays were performed at room temperature (22 ± 1°C) using a Nikon Eclipse Ti-U inverted microscope equipped with a Plan Apo 100× 1.49 N.A. oil emersion lens for epifluorescence or through-the-objective total internal reflectance microscopy (TIRFM) using a custom “Micro Optic Fiber Launch TIRFM” (patent pending) as described (14 (link)). Briefly, either a Lumen 200-W metal arc lamp (Prior Scientific) or 532-nm diode-pumped, solid-state, 50-mW laser (Lasever Inc.) was used for excitation. Images were obtained using an intensified high-resolution 10-bit digital camera (XR/Turbo-Z running Piper Control v2.6.09 software, Stanford Photonics).
Previs M.J., Prosser B.L., Mun J.Y., Previs S.B., Gulick J., Lee K., Robbins J., Craig R., Lederer W.J, & Warshaw D.M. (2015). Myosin-binding protein C corrects an intrinsic inhomogeneity in cardiac excitation-contraction coupling. Science Advances, 1(1), e1400205.
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3

Thin Filament Sliding Assay Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
All native thin filament sliding assays were performed at room temperature (22 ± 1°C) using a Nikon Eclipse Ti-U inverted microscope equipped with a Plan Apo 100× 1.49 N.A. oil emersion lens for epifluorescence or through-the-objective total internal reflectance microscopy (TIRFM) using a custom “Micro Optic Fiber Launch TIRFM” (patent pending) as described (14 (link)). Briefly, either a Lumen 200-W metal arc lamp (Prior Scientific) or 532-nm diode-pumped, solid-state, 50-mW laser (Lasever Inc.) was used for excitation. Images were obtained using an intensified high-resolution 10-bit digital camera (XR/Turbo-Z running Piper Control v2.6.09 software, Stanford Photonics).
Previs M.J., Prosser B.L., Mun J.Y., Previs S.B., Gulick J., Lee K., Robbins J., Craig R., Lederer W.J, & Warshaw D.M. (2015). Myosin-binding protein C corrects an intrinsic inhomogeneity in cardiac excitation-contraction coupling. Science Advances, 1(1), e1400205.
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