xm10 digital camera (Olympus)
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xm10 digital camera
Xm10 Digital Camera, supplied by Olympus, used in various techniques. Bioz Stars score: 96/100, based on 327 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/xm10+digital+microscope+camera/XM10%2FXM10-IR+Microscope+Digital+Camera/pm41754260-129-18-21
Average 96 stars, based on 327 article reviews
Xm10 Digital Camera, supplied by Olympus, used in various techniques. Bioz Stars score: 96/100, based on 327 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/xm10+digital+microscope+camera/XM10%2FXM10-IR+Microscope+Digital+Camera/pm41754260-129-18-21
Average 96 stars, based on 327 article reviews
xm10 digital camera - by Bioz Stars,
2026-10
96/100 stars
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Inverted Microscopy:Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction. Article Snippet: Two additional slides (slide 2 and 13) were incubated with 100 μL of DAPI for 30 min. After rinsing them twice using DPBS, they were mounted in a VECTASHIELD Antifade mounting medium (Vector Laboratories, Newark, CA, US). .. The slides were subjected to z-stack acquisition to visualize the NIR dye AF750 as well as DAPI within the same FOV using a 63× oil objective on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction. Article Snippet: HeLa pLuc 705 cells12 (obtained within the IMI collaborative project COMPACT, grant agreement no. 115363) were grown in Dulbecco’s modified Eagle medium (DMEM) high glucose supplemented with 10% FCS (Biowest, Riverside, MO, USA), 1% penicillin-streptomycin (Sigma-Aldrich), 2% L-glutamine (SigmaAldrich), and 200 μg mL−1 hygromycin B. HeLa wild-type (CCL2, ATCC, Manassas, USA) and HeLa mRuby-3 galectin 8 cells (see section 5.7) were grown in the same medium without hygromycin B. CT26-Luc cells were cultured in DMEM/F12 medium (1:1) supplemented with 10% FCS, 1% penicillin-streptomycin, and 1% Lglutamine; luciferase expression was confirmed on the day of injection using the GloMax Navigator System (GM2010, Promega). .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL−1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction Article Snippet: .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL –1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction Article Snippet: Two additional slides (slide 2 and 13) were incubated with 100 μL of DAPI for 30 min. After rinsing them twice using DPBS, they were mounted in a VECTASHIELD Antifade mounting medium (Vector Laboratories, Newark, CA, US). .. The slides were subjected to z-stack acquisition to visualize the NIR dye AF750 as well as DAPI within the same FOV using a 63× oil objective on an Olympus IX73 inverted microscope with an Olympus Microscopy:Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction. Article Snippet: Two additional slides (slide 2 and 13) were incubated with 100 μL of DAPI for 30 min. After rinsing them twice using DPBS, they were mounted in a VECTASHIELD Antifade mounting medium (Vector Laboratories, Newark, CA, US). .. The slides were subjected to z-stack acquisition to visualize the NIR dye AF750 as well as DAPI within the same FOV using a 63× oil objective on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction. Article Snippet: HeLa pLuc 705 cells12 (obtained within the IMI collaborative project COMPACT, grant agreement no. 115363) were grown in Dulbecco’s modified Eagle medium (DMEM) high glucose supplemented with 10% FCS (Biowest, Riverside, MO, USA), 1% penicillin-streptomycin (Sigma-Aldrich), 2% L-glutamine (SigmaAldrich), and 200 μg mL−1 hygromycin B. HeLa wild-type (CCL2, ATCC, Manassas, USA) and HeLa mRuby-3 galectin 8 cells (see section 5.7) were grown in the same medium without hygromycin B. CT26-Luc cells were cultured in DMEM/F12 medium (1:1) supplemented with 10% FCS, 1% penicillin-streptomycin, and 1% Lglutamine; luciferase expression was confirmed on the day of injection using the GloMax Navigator System (GM2010, Promega). .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL−1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction Article Snippet: .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL –1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction Article Snippet: Two additional slides (slide 2 and 13) were incubated with 100 μL of DAPI for 30 min. After rinsing them twice using DPBS, they were mounted in a VECTASHIELD Antifade mounting medium (Vector Laboratories, Newark, CA, US). .. The slides were subjected to z-stack acquisition to visualize the NIR dye AF750 as well as DAPI within the same FOV using a 63× oil objective on an Olympus IX73 inverted microscope with an Olympus Staining:Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction. Article Snippet: HeLa pLuc 705 cells12 (obtained within the IMI collaborative project COMPACT, grant agreement no. 115363) were grown in Dulbecco’s modified Eagle medium (DMEM) high glucose supplemented with 10% FCS (Biowest, Riverside, MO, USA), 1% penicillin-streptomycin (Sigma-Aldrich), 2% L-glutamine (SigmaAldrich), and 200 μg mL−1 hygromycin B. HeLa wild-type (CCL2, ATCC, Manassas, USA) and HeLa mRuby-3 galectin 8 cells (see section 5.7) were grown in the same medium without hygromycin B. CT26-Luc cells were cultured in DMEM/F12 medium (1:1) supplemented with 10% FCS, 1% penicillin-streptomycin, and 1% Lglutamine; luciferase expression was confirmed on the day of injection using the GloMax Navigator System (GM2010, Promega). .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL−1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus Article Title: Accelerated Endosomal Escape of Splice-Switching Oligonucleotides Enables Efficient Hepatic Splice Correction Article Snippet: .. Cells were washed two more times, and nuclei were stained using DAPI at 2 μg mL –1 for 20 min. After washing, cells were covered in DPBS (100 μL) and imaged with a 20-fold magnification on an Olympus IX73 inverted microscope with an Olympus |