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standard light microscope equipped with a stage warmer  (Nikon)


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    Nikon standard light microscope equipped with a stage warmer
    Standard Light Microscope Equipped With A Stage Warmer, supplied by Nikon, 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/result/standard light microscope equipped with a stage warmer/product/Nikon
    Average 90 stars, based on 1 article reviews
    standard light microscope equipped with a stage warmer - by Bioz Stars, 2026-06
    90/100 stars

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    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of <t>spermatozoa</t> with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.
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    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of <t>spermatozoa</t> with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.
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    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of <t>spermatozoa</t> with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.
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    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of <t>spermatozoa</t> with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.
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    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of <t>spermatozoa</t> with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.
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    https://www.bioz.com/result/microscope glass stage warmers/product/Tokai Hit Co Ltd
    Average 90 stars, based on 1 article reviews
    microscope glass stage warmers - by Bioz Stars, 2026-06
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    Image Search Results


    Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of spermatozoa with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Melatonin Attenuates Chromium (VI)-Induced Spermatogonial Stem Cell/Progenitor Mitophagy by Restoration of METTL3-Mediated RNA N 6 -Methyladenosine Modification

    doi: 10.3389/fcell.2021.684398

    Figure Lengend Snippet: Chromium (Cr) (VI) damaged male reproductive system and spermatogonial stem cells (SSCs)/progenitors in mouse testes. (A) Hematoxylin and eosin (H&E) staining of testis sections from control and Cr (VI)-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in control and Cr (VI)-treated mouse testes. (E) The average body weight in control and Cr (VI)-treated mice. (F) The average testicular index (testis weight/body weight) in control and Cr (VI)-treated mice. (G) The average sperm number (10 6 /ml) in control and Cr (VI)-treated mice. (H) The ratio of spermatozoa with progressive motility in control and Cr (VI)-treated mice. (I) Left: the ratio of abnormal spermatozoa in control and Cr (VI)-treated mice; Right: images of spermatozoa from the control and Cr (VI)-treated mice. Bar = 50 μm. (J,K) Immunofluorescence staining for LIN28 (J) and CDH1 (K) in testis sections from control and Cr (VI)-treated mice. Bar = 100 μm. (L,M) The numbers of LIN28 + (L) and CDH1 + cells (M) per seminiferous tubule in control and Cr (VI)-treated mouse testes. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. ** p < 0.01.

    Article Snippet: A minimum of 300 spermatozoa were observed from at least five randomly selected fields with 20 μm CELL-VU® DRM-600 sperm count slides (Millennium Sciences, United States) and a microscopic stage warmer (KITAZATO, Japan).

    Techniques: Staining, Control, Immunofluorescence

    Melatonin alleviated Cr (VI)-induced damage to male reproductive system and autophagy in mouse testes. (A) H&E staining of testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in testes from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. (E) The average body weight in different mouse groups. (F) The average testicular index (testis weight/body weight) in different mouse groups. (G) The average sperm number (10 6 /ml) in different mouse groups. (H) The ratio of spermatozoa with progressive motility in different mouse groups. (I) The upper panel: the ratio of abnormal spermatozoa in different mouse groups; The lower panel: images of spermatozoa from different groups of mice. Bar = 50 μm. (J) Immunofluorescence staining for LIN28 in testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 200 μm. (K) The numbers of LIN28 + cells per seminiferous tubule in testes from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. (L) Co-staining analysis for LC3 and LIN28 in testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 100 μm. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. * p < 0.05; ** p < 0.01.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Melatonin Attenuates Chromium (VI)-Induced Spermatogonial Stem Cell/Progenitor Mitophagy by Restoration of METTL3-Mediated RNA N 6 -Methyladenosine Modification

    doi: 10.3389/fcell.2021.684398

    Figure Lengend Snippet: Melatonin alleviated Cr (VI)-induced damage to male reproductive system and autophagy in mouse testes. (A) H&E staining of testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 200 μm. (B–D) The ratios of only 1–3 layers of germ cell (B) , empty (C) , and abnormal (D) seminiferous tubules in testes from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. (E) The average body weight in different mouse groups. (F) The average testicular index (testis weight/body weight) in different mouse groups. (G) The average sperm number (10 6 /ml) in different mouse groups. (H) The ratio of spermatozoa with progressive motility in different mouse groups. (I) The upper panel: the ratio of abnormal spermatozoa in different mouse groups; The lower panel: images of spermatozoa from different groups of mice. Bar = 50 μm. (J) Immunofluorescence staining for LIN28 in testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 200 μm. (K) The numbers of LIN28 + cells per seminiferous tubule in testes from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. (L) Co-staining analysis for LC3 and LIN28 in testis sections from the control, Cr (VI), melatonin + Cr (VI), and melatonin-treated mice. Bar = 100 μm. Data are presented as the mean ± SEM from five mice, and 300 seminiferous tubules from five mice were analyzed in each group. * p < 0.05; ** p < 0.01.

    Article Snippet: A minimum of 300 spermatozoa were observed from at least five randomly selected fields with 20 μm CELL-VU® DRM-600 sperm count slides (Millennium Sciences, United States) and a microscopic stage warmer (KITAZATO, Japan).

    Techniques: Staining, Control, Immunofluorescence