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iplab software for macintosh  (scanalytics inc)

 
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    scanalytics inc iplab software for macintosh
    Iplab Software For Macintosh, supplied by scanalytics inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iplab+macintosh+software/iplab+software+for+macintosh/pm38876319-144-13-17
    Average 90 stars, based on 1 article reviews
    iplab software for macintosh - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Software:

    Article Title: Cold shock and regulation of surface protein trafficking convey sensitization to inducers of stage differentiation in Trypanosoma brucei
    Article Snippet: .. The microscopic set-up was integrated and controlled using the scripting feature of the IPLab for Macintosh software (version 3.2; Scanalytics). ..

    Article Title: Ovine model for engineering bone segments.
    Article Snippet: We propose a large animal model for bone tissue engineering that yields quantitative data and simulates clinical methods and tissue needs.. Skeletally mature domestic sheep (n 20) were each implanted with three rectangular (1 1 4 cm), hollow tissue-molding chambers that were empty (control) or filled with equal weights (6.71–6.78 g) of particulate autologous bone graft (MBG) or bone graft that was autoclaved to denature stored growth factors (DeMBG).. MBG provided scaffold and bioactive factors, and DeMBG provided only scaffold.

    Article Title: Pag1p, a Novel Protein Associated with Protein Kinase Cbk1p, Is Required for Cell Morphogenesis and Proliferation in Saccharomyces cerevisiae
    Article Snippet: Microscopy For light microscopy, samples were viewed on a Zeiss Axiophot 2 microscope (Zeiss, Pberkochen, Germany) by using a 63 or 100× oil-immersion objective (numerical aperture 1.4). .. Images were acquired with a Photometrics Quantix charge-coupled device camera (Tuscon, AZ) by using IPLab for Macintosh software (Scanalytics, Fairfax, VA). ..

    Article Title: Targeting the Variable Surface of African Trypanosomes with Variant Surface Glycoprotein-Specific, Serum-Stable RNA Aptamers
    Article Snippet: For acquisition of three-dimensional images a PIFOC objective z-stepper was driven by the piezo-amplifier E662 LVPZT (Physik Instrumente, Karlsruhe, Germany). .. The microscopic setup was integrated and controlled by using the scripting feature of the IPLab for Macintosh software (v3.2; Scanalytics, Fairfax, Va.). ..



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    Fos expression in control and stimulated animals. The brain areas that were examined were the substantia nigra pars reticulate (SNr) (a–d), entopeduncular nucleus (EP) (e–h), and nucleus accumbens shell (NAsh) (i–l). Left panels for each structure show images that were taken from control rats, and right panels show images that were taken from stimulated rats. Orientation is noted at 2.5 × magnification (left panels), and cell counts were taken at 20 × magnification (right panels). Arrows highlight a typical Fos-positive neuron for each section. Scale bars=100 μm. (m) The quantification of Fos expression in each structure is illustrated for control rats (empty bars) and subthalamic nucleus high-frequency stimulation (STN HFS) rats (black bars) and was calculated using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision). *p<0.05, significant effect compared with control group. Error bars indicate SEM. PFC, prefrontal cortex.
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    Fos expression in control and stimulated animals. The brain areas that were examined were the substantia nigra pars reticulate (SNr) (a–d), entopeduncular nucleus (EP) (e–h), and nucleus accumbens shell (NAsh) (i–l). Left panels for each structure show images that were taken from control rats, and right panels show images that were taken from stimulated rats. Orientation is noted at 2.5 × magnification (left panels), and cell counts were taken at 20 × magnification (right panels). Arrows highlight a typical Fos-positive neuron for each section. Scale bars=100 μm. (m) The quantification of Fos expression in each structure is illustrated for control rats (empty bars) and subthalamic nucleus high-frequency stimulation (STN HFS) rats (black bars) and was calculated using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision). *p<0.05, significant effect compared with control group. Error bars indicate SEM. PFC, prefrontal cortex.
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    Fos expression in control and stimulated animals. The brain areas that were examined were the substantia nigra pars reticulate (SNr) (a–d), entopeduncular nucleus (EP) (e–h), and nucleus accumbens shell (NAsh) (i–l). Left panels for each structure show images that were taken from control rats, and right panels show images that were taken from stimulated rats. Orientation is noted at 2.5 × magnification (left panels), and cell counts were taken at 20 × magnification (right panels). Arrows highlight a typical Fos-positive neuron for each section. Scale bars=100 μm. (m) The quantification of Fos expression in each structure is illustrated for control rats (empty bars) and subthalamic nucleus high-frequency stimulation (STN HFS) rats (black bars) and was calculated using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision). *p<0.05, significant effect compared with control group. Error bars indicate SEM. PFC, prefrontal cortex.
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    Fos expression in control and stimulated animals. The brain areas that were examined were the substantia nigra pars reticulate (SNr) (a–d), entopeduncular nucleus (EP) (e–h), and nucleus accumbens shell (NAsh) (i–l). Left panels for each structure show images that were taken from control rats, and right panels show images that were taken from stimulated rats. Orientation is noted at 2.5 × magnification (left panels), and cell counts were taken at 20 × magnification (right panels). Arrows highlight a typical Fos-positive neuron for each section. Scale bars=100 μm. (m) The quantification of Fos expression in each structure is illustrated for control rats (empty bars) and subthalamic nucleus high-frequency stimulation (STN HFS) rats (black bars) and was calculated using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision). *p<0.05, significant effect compared with control group. Error bars indicate SEM. PFC, prefrontal cortex.

    Journal: Neuropsychopharmacology

    Article Title: High-Frequency Stimulation of the Subthalamic Nucleus Blocks Compulsive-Like Re-Escalation of Heroin Taking in Rats

    doi: 10.1038/npp.2016.270

    Figure Lengend Snippet: Fos expression in control and stimulated animals. The brain areas that were examined were the substantia nigra pars reticulate (SNr) (a–d), entopeduncular nucleus (EP) (e–h), and nucleus accumbens shell (NAsh) (i–l). Left panels for each structure show images that were taken from control rats, and right panels show images that were taken from stimulated rats. Orientation is noted at 2.5 × magnification (left panels), and cell counts were taken at 20 × magnification (right panels). Arrows highlight a typical Fos-positive neuron for each section. Scale bars=100 μm. (m) The quantification of Fos expression in each structure is illustrated for control rats (empty bars) and subthalamic nucleus high-frequency stimulation (STN HFS) rats (black bars) and was calculated using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision). *p<0.05, significant effect compared with control group. Error bars indicate SEM. PFC, prefrontal cortex.

    Article Snippet: Labeled cells from three sections per rat were bilaterally and automatically counted using IPLab 3.9.4 r5 software for Macintosh (Scanalytics) and iVision 4.0.15 software for Macintosh (BioVision).

    Techniques: Expressing, Software