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3ccd color video camera

Manufactured by Sony
Sourced in Japan

The 3CCD color video camera is a high-quality video imaging device that captures color images using three separate charge-coupled device (CCD) sensors, one each for the red, green, and blue color channels. This design ensures accurate color reproduction and high-resolution video output. The camera's core function is to provide a reliable and versatile solution for various video capture applications.

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7 protocols using 3ccd color video camera

1

PD-L1 Immunohistochemistry in Mouse Skin

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Samples were fixed and embedded as above and staining was performed
by hand using the Novus PD-L1 antibody NBP1–43262 at a 1:20 dilution.
The secondary antibody was from Vector Laboratories, BA-9401 goat anti-rat
at a 1:50 dilution. NIH3T3 cell pellet sections (mouse cells) were used as
positive controls, while mouse cSCC and mouse skin were exposed to secondary
antibody only as negative controls.
Mouse epidermal staining for PD-L1 was quantified using the ImagePro
Plus (Media Cybernetics software system, a Leica DMR microscope, and a Sony
3CCD color video camera [11 (link)]. The
mean positive cytoplasmic staining area per 20x field was determined for
each sample, measuring 3 fields/slide, 3 mice per time point.
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2

Histological Tissue Analysis of Mice

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The liver, lung, kidney and heart tissues of mice from the different groups were collected and fixed with 10% neutral formaldehyde solution for 24 h. The samples were dehydrated by a tissue-dehydrating machine, embedded in paraffin and sectioned into 4-μm thick slices. Following roasting, slicing and dewaxing, routine hematoxylin-eosin staining was conducted and the sections were observed under light microscopy using an Olympus BX40F microscope (Olympus, Melville, NY, USA). Images were captured with a Sony 3CCD color video camera (Sony, Tokyo, Japan).
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3

Quantifying Neuronal Survival in Hippocampal CA1 Region after Ischemic Injury

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The number of normal neurons was counted as described earlier (Dave et al., 2005 (link)). In brief, on day 14 post-ischemia/sham surgery, rats were perfused using FAM (a mixture of 40% formaldehyde, glacial acetic acid, and methanol, 1:1:8 by volume) under isoflurane anesthesia for histological analysis. Coronal sections were made from paraffin-embedded brains and stained with hematoxylin and eosin. In sections containing hippocampus at the level of -3.6, -3.8, and -4.0 mm from bregma, the number of surviving normal neurons within the entire CA1 region of hippocampus was counted using MCID Elite 6.0 software (InterFocus Imaging Ltd, Cambridge, UK) attached to a Nikon microscope (Nikon Microphot-SA; Nikon Corporation, Tokyo, Japan), a Sony 3CCD color video camera (Sony Corporation, Tokyo, Japan), and an LEP motorized stage (Ludl Electronic Products Ltd, Hawthorne, NY). The counts at the three bregma levels were averaged.
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4

Bovine Embryo-nfeAFP11 Interaction Dynamics

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Bovine embryos were incubated with nfeAFP11 labelled with the fluorescent probe Alexa 488 (Invitrogen, Carlsbad, CA, USA) in phosphate buffered saline (PBS) at 4–5 C (Medicool, Sanyo, Osaka, Japan), 19–23 C (room temperature, RT) or 37 C (MIR–162 incubator, Sanyo) for 10, 20, 30 and 60 min. After incubation, the embryos were washed several times in PBS supplemented with 5% FBS (MP Biomedicals, Illkirch, France) and mounted under cover slips without compression in medium containing 50% glycerol and 25 mg/ml of sodium azide. Interaction between bovine embryos and nfeAFP11 was observed using a Leica DM LD fluorescence microscope (Leica, Wetzlar, Germany) at an excitation/emission wavelength of 485/530 nm. The morphology of the chilled embryos was evaluated using light microscopy (Leica Wild M3Z, Leica), and all the photomicroscope images were recorded using an Olympus DP21 microscope digital camera (Olympus, Tokyo, Japan). Individual mean pixel intensity was measured on a
per embryo basis using the ImageJ software (National Institutes of Health, Bethesda, MD, USA). Furthermore, a Leica DM IRE2 confocal microscope system (Leica) was also used to observe nfeAFP11-embryo interactions. The embryos were incubated with nfeAFP11 labelled with Alexa 488 in PBS at RT or 37 C for 30 min. All the confocal microscope images were recorded using a 3CCD color video camera (Sony, Tokyo, Japan).
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5

Muscle Fiber Diameter Quantification

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All slides were examined with a Zeiss Axiophot 200 light microscope coupled to a Sony 3CCD Color Video Camera. Up to 10 digital pictures were taken from each cross section with 10-fold magnification (10-fold objective) (Figure 3). A digital micrometer scale was applied to set the correct μm/pixel ratio for this magnification level. 1.2 pixel determined a length of 1 μm and this aspect ratio was used for all photos. Myofiber diameter was quantified by selection of the sarcoplasmic region within the borders of the sarcolemma of the myofiber and its subsequent measurement by the best fitting ellipse tool (Cluff et al., 2013 (link)) using the software ImageJ® (National Institutes of Health, United States). The minor axis was determined as the diameter of the myofiber. 55.4 ± 8.2 type I and type II myofibers per subject and time point analyses for changes in myofiber diameter.
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6

Histological and Ultrastructural Analysis of Kidney Tissues

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Kidneys were flushed with phosphate-buffered saline and then fixed in 4% paraformaldehyde for 48 hours. After fixation, tissues were washed and transferred to phosphate-buffered saline. Tissues were embedded in glycol methacrylate or low-melting point paraffin, and sections were cut at a thickness of 4 μm and stained with periodic acid Schiff (PAS) [25 (link)]. For electron microscopy, tissues were fixed for 1 hour in 1.0% osmium tetroxide, prestained in 1.25% uranyl acetate for 1 hour, dehydrated through a series of graded alcohol solutions, and embedded in EPON epoxy resin. The severity of histological lesions in tunicamycin-treated old and young mice was determined using a Meta Imaging software (Molecular Devices, Downingtown, PA, USA). The injured proximal tubules in the cortical area were digitized under a microscope connected with a Sony 3CCD color video camera. The ratio of the damaged to normal tubular area was measured [26 (link)].
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7

Measuring Tracheal Ciliary Beat Frequency

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Tracheal CBF was measured using a light microscope (Olympus BX 50, Tokyo, Japan) connected to a video camera (Sony -3CCD-color video camera) and a video monitor. A stroboscope (Machine Vision Strobe, Cedar Hurst, NY) was placed in front of the tracheal tissue fragment and emitted light flashes at a rate varying between 0 and 30 Hz, based on synchronization with the cilia movements. [13 (link)]
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