nis elements ar software version 6 22 01 (Nikon)
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nis elements ar software version 6 22 01
Nis Elements Ar Software Version 6 22 01, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 39798 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nis+elements+ar+software+version+6+22+01/NIS-Elements/pm41750293-52-68-74
Average 99 stars, based on 39798 article reviews
Nis Elements Ar Software Version 6 22 01, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 39798 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nis+elements+ar+software+version+6+22+01/NIS-Elements/pm41750293-52-68-74
Average 99 stars, based on 39798 article reviews
nis elements ar software version 6 22 01 - by Bioz Stars,
2026-09
99/100 stars
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Microscopy:Article Title: Molecular Motors Orchestrate Pause-and-Run Dynamics to Facilitate Intracellular Transport Article Snippet: For immunofluorescence cell staining, BEAS-2B cells were generally fixed in −20 °C methanol for 10 min, and then blocked with 4% bovine serum albumin (BSA; Sigma-Aldrich) in PBS at room temperature for 2 h. Next, cells were incubated with primary antibodies against detyrosinated tubulin (1:200) and α-tubulin (1:500), and corresponding secondary antibodies (1:200), each for 1 h. Stained cells were mounted onto a microscope slide with ProLongTM Gold Antifade Mountant (Invitrogen) and then examined using spinning disk confocal microscopy. .. The spinning disk confocal was performed on an inverted research microscope Eclipse Ti2-E with the Perfect Focus System (Nikon, Tokyo, Japan), equipped with a Plan Apo 60× NA 1.40 oil objective, a Crest X-Light V3 spinning disk confocal head (Crest-Optics, Rome, Italy), a Celesta light engine (Lumencor, Beaverton, OR, USA) as the light source, a Prime 95B 25MM sCMOS camera (Teledyne Photometrics, Tucson, AZ, USA) and controlled by Article Title: Molecular Motors Orchestrate Pause-and-Run Dynamics to Facilitate Intracellular Transport. Article Snippet: For immunofluorescence cell staining, BEAS-2B cells were generally fixed in −20 ◦C methanol for 10 min, and then blocked with 4% bovine serum albumin https://doi.org/10.3390/biom16020221 (BSA; Sigma-Aldrich) in PBS at room temperature for 2 h. Next, cells were incubated with primary antibodies against detyrosinated tubulin (1:200) and α-tubulin (1:500), and corresponding secondary antibodies (1:200), each for 1 h. Stained cells were mounted onto a microscope slide with ProLongTM Gold Antifade Mountant (Invitrogen) and then examined using spinning disk confocal microscopy. .. The spinning disk confocal was performed on an inverted research microscope Eclipse Ti2-E with the Perfect Focus System (Nikon, Tokyo, Japan), equipped with a Plan Apo 60× NA 1.40 oil objective, a Crest X-Light V3 spinning disk confocal head (Crest-Optics, Rome, Italy), a Celesta light engine (Lumencor, Beaverton, OR, USA) as the light source, a Prime 95B 25MM sCMOS camera (Teledyne Photometrics, Tucson, AZ, USA) and controlled by Software:Article Title: Molecular Motors Orchestrate Pause-and-Run Dynamics to Facilitate Intracellular Transport Article Snippet: For immunofluorescence cell staining, BEAS-2B cells were generally fixed in −20 °C methanol for 10 min, and then blocked with 4% bovine serum albumin (BSA; Sigma-Aldrich) in PBS at room temperature for 2 h. Next, cells were incubated with primary antibodies against detyrosinated tubulin (1:200) and α-tubulin (1:500), and corresponding secondary antibodies (1:200), each for 1 h. Stained cells were mounted onto a microscope slide with ProLongTM Gold Antifade Mountant (Invitrogen) and then examined using spinning disk confocal microscopy. .. The spinning disk confocal was performed on an inverted research microscope Eclipse Ti2-E with the Perfect Focus System (Nikon, Tokyo, Japan), equipped with a Plan Apo 60× NA 1.40 oil objective, a Crest X-Light V3 spinning disk confocal head (Crest-Optics, Rome, Italy), a Celesta light engine (Lumencor, Beaverton, OR, USA) as the light source, a Prime 95B 25MM sCMOS camera (Teledyne Photometrics, Tucson, AZ, USA) and controlled by Article Title: Molecular Motors Orchestrate Pause-and-Run Dynamics to Facilitate Intracellular Transport. Article Snippet: For immunofluorescence cell staining, BEAS-2B cells were generally fixed in −20 ◦C methanol for 10 min, and then blocked with 4% bovine serum albumin https://doi.org/10.3390/biom16020221 (BSA; Sigma-Aldrich) in PBS at room temperature for 2 h. Next, cells were incubated with primary antibodies against detyrosinated tubulin (1:200) and α-tubulin (1:500), and corresponding secondary antibodies (1:200), each for 1 h. Stained cells were mounted onto a microscope slide with ProLongTM Gold Antifade Mountant (Invitrogen) and then examined using spinning disk confocal microscopy. .. The spinning disk confocal was performed on an inverted research microscope Eclipse Ti2-E with the Perfect Focus System (Nikon, Tokyo, Japan), equipped with a Plan Apo 60× NA 1.40 oil objective, a Crest X-Light V3 spinning disk confocal head (Crest-Optics, Rome, Italy), a Celesta light engine (Lumencor, Beaverton, OR, USA) as the light source, a Prime 95B 25MM sCMOS camera (Teledyne Photometrics, Tucson, AZ, USA) and controlled by |