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mac scope software version 2.5  (Fukui Bank Ltd)

 
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    Fukui Bank Ltd mac scope software version 2.5
    Mac Scope Software Version 2.5, supplied by Fukui Bank Ltd, 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/mac+scope+computer+software/mac+scope+software+version+2+5/pm22785176-118-7-13
    Average 90 stars, based on 1 article reviews
    mac scope software version 2.5 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Software:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..

    Immunohistochemistry:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..

    Saline:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..

    Blocking Assay:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..

    Amplification:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..

    Labeling:

    Article Title: Targeted expression of a pan-caspase inhibitor in tubular epithelium attenuates interstitial inflammation and fibrogenesis in nephritic but not nephrotic mice.
    Article Snippet: .. Interstitial fibrosis was quantitatively determined with the Mac SCOPE software version 2.5 (Mitani, Fukui, Japan) in 10 high-power ( 200) cortical fields, and the interstitial fibrosis indices were expressed as the mean percentage area in blue per cortical field in Masson’s trichrome–stained sections.13 Glomerular damage such as sclerosis and crescent formation was quantitatively determined with the Mac SCOPE software in 30 glomeruli, and the glomerular damage indices were expressed as the mean percentage of sclerotic/crescentic area per glomerulus.41 For immunohistochemistry, the antibodies against p3515 (a generous gift from Professor M. Miura), singlestranded DNA17 (18731; Immuno-Biological Laboratories, Fujioka, Japan), mouse monocytes (F4/80; AbD Serotec, Oxford, UK), and fibroblasts (FSP1)42 were diluted (1:400) into 1% bovine serum albumin in phosphate-buffered saline as the blocking buffer, and then applied on the sections for 8 h. Signals were amplified using the TSA kit (Molecular Probe/Invitrogen, Carlsbad, CA) and labeled using Alexa Fluor 555 (Molecular Probe) according to a conventional indirect method. ..



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