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compound optical microscope bx4; 100x magnification  (Evident Corporation)

 
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    Structured Review

    Evident Corporation compound optical microscope bx4; 100x magnification
    Compound Optical Microscope Bx4; 100x Magnification, supplied by Evident Corporation, 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/bx4+microscope/bx51+microscope/pm38103621-120-7-10
    Average 90 stars, based on 1 article reviews
    compound optical microscope bx4; 100x magnification - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Software:

    Article Title: Aortic Stiffness in L-NAME Treated C57Bl/6 Mice Displays a Shift From Early Endothelial Dysfunction to Late-Term Vascular Smooth Muscle Cell Dysfunction
    Article Snippet: .. Microscopic images were acquired with universal Grap 6.1 software using an Olympus BX4 microscope and quantified using ImageJ software. .. The suprarenal abdominal aorta was lysed in Laemmli sample buffer (Bio-Rad) containing 5% β-mercaptoethanol.

    Article Title: Disparate biomechanical properties of the aorta in non‐aneurysmal and aneurysmal mice treated with angiotensin II
    Article Snippet: .. Microscopic images were acquired with Universal Grap 6.1 software using an Olympus BX4 microscope or Celena S fluorescence microscope and quantified using ImageJ software. ..

    Article Title: Curcumin and Vitamin C Attenuate Gentamicin-Induced Nephrotoxicity by Modulating Distinctive Reactive Species
    Article Snippet: .. An Olympus BX4 microscope was used to examine the obtained preparations, and the Olympus UC30 camera and Stream Basic software were used to take the images. ..

    Article Title: Aortic Stiffness in L-NAME Treated C57Bl/6 Mice Displays a Shift From Early Endothelial Dysfunction to Late-Term Vascular Smooth Muscle Cell Dysfunction.
    Article Snippet: .. Microscopic images were acquired with universal Grap 6.1 software using an Olympus BX4 microscope and quantified using ImageJ software. ..

    Microscopy:

    Article Title: Aortic Stiffness in L-NAME Treated C57Bl/6 Mice Displays a Shift From Early Endothelial Dysfunction to Late-Term Vascular Smooth Muscle Cell Dysfunction
    Article Snippet: .. Microscopic images were acquired with universal Grap 6.1 software using an Olympus BX4 microscope and quantified using ImageJ software. .. The suprarenal abdominal aorta was lysed in Laemmli sample buffer (Bio-Rad) containing 5% β-mercaptoethanol.

    Article Title: Disparate biomechanical properties of the aorta in non‐aneurysmal and aneurysmal mice treated with angiotensin II
    Article Snippet: .. Microscopic images were acquired with Universal Grap 6.1 software using an Olympus BX4 microscope or Celena S fluorescence microscope and quantified using ImageJ software. ..

    Article Title: Curcumin and Vitamin C Attenuate Gentamicin-Induced Nephrotoxicity by Modulating Distinctive Reactive Species
    Article Snippet: .. An Olympus BX4 microscope was used to examine the obtained preparations, and the Olympus UC30 camera and Stream Basic software were used to take the images. ..

    Article Title: The differential cancer growth associated with anaesthetics in a cancer xenograft model of mice: mechanisms and implications of postoperative cancer recurrence
    Article Snippet: Slides were counterstained with Vectashield mounting medium containing DAPI (Millipore, Watfield, UK). .. Slides were viewed under Olympus BX4 microscope (Olympus, Hamburg, Germany). ..

    Article Title: Micro-PET imaging of hepatitis C virus NS3/4A protease activity using a protease-activatable retention probe
    Article Snippet: The adjacent tumor sections either directly detect the FITC-fluorescent intensity to observe the accumulation of TAT-ΔNS3/4A-FITC probe or stained with a 520 HCV protease Assay Kit (AnaSpec) to visualize NS3/4A activity. .. The sections were examined on an upright BX4 microscope (Olympus, Melville, NY, USA) or viewed under phase contrast or fluorescence fields on an inverted Axiovert 200 microscope (Carl Zeiss Microimaging, Thornwood, NY, USA). .. 124 I was purchased from IBA Molecular, VA, USA (2.6 TBq/mL, n.c.a.).

    Article Title: ReMOT Control Delivery of CRISPR-Cas9 Ribonucleoprotein Complex to Induce Germline Mutagenesis in the Disease Vector Mosquitoes Culex pipiens pallens (Diptera: Culicidae).
    Article Snippet: The wide distribution of Culex (Cx.) pipiens complex mosquitoes makes it difficult to prevent the transmission of mosquito-borne diseases in humans.. Gene editing using CRISPR/Cas9 is an effective technique with the potential to solve the growing problem of mosquito-borne diseases.. This study uses the ReMOT Control technique in Culex pipiens pallens (L.) to produce genetically modified mosquitoes.

    Article Title: Regulated cell death and inflammasome activation in gut injury following traumatic surgery in vitro and in vivo: implication for postoperative death due to multiorgan dysfunction.
    Article Snippet: .. Slides were viewed under Olympus BX4 microscope and representative images for each group were taken. .. Tissue and cell samples were homogenised with cell lysis buffer (Cell Signaling Technology) supplemented with protease inhibitor (11873580001, Roche, Switzerland) and phosphatase inhibitor (4906845001, Roche).

    Article Title: Aortic Stiffness in L-NAME Treated C57Bl/6 Mice Displays a Shift From Early Endothelial Dysfunction to Late-Term Vascular Smooth Muscle Cell Dysfunction.
    Article Snippet: .. Microscopic images were acquired with universal Grap 6.1 software using an Olympus BX4 microscope and quantified using ImageJ software. ..

    Fluorescence:

    Article Title: Disparate biomechanical properties of the aorta in non‐aneurysmal and aneurysmal mice treated with angiotensin II
    Article Snippet: .. Microscopic images were acquired with Universal Grap 6.1 software using an Olympus BX4 microscope or Celena S fluorescence microscope and quantified using ImageJ software. ..

    Article Title: Micro-PET imaging of hepatitis C virus NS3/4A protease activity using a protease-activatable retention probe
    Article Snippet: The adjacent tumor sections either directly detect the FITC-fluorescent intensity to observe the accumulation of TAT-ΔNS3/4A-FITC probe or stained with a 520 HCV protease Assay Kit (AnaSpec) to visualize NS3/4A activity. .. The sections were examined on an upright BX4 microscope (Olympus, Melville, NY, USA) or viewed under phase contrast or fluorescence fields on an inverted Axiovert 200 microscope (Carl Zeiss Microimaging, Thornwood, NY, USA). .. 124 I was purchased from IBA Molecular, VA, USA (2.6 TBq/mL, n.c.a.).

    Transferring:

    Article Title: ReMOT Control Delivery of CRISPR-Cas9 Ribonucleoprotein Complex to Induce Germline Mutagenesis in the Disease Vector Mosquitoes Culex pipiens pallens (Diptera: Culicidae).
    Article Snippet: The wide distribution of Culex (Cx.) pipiens complex mosquitoes makes it difficult to prevent the transmission of mosquito-borne diseases in humans.. Gene editing using CRISPR/Cas9 is an effective technique with the potential to solve the growing problem of mosquito-borne diseases.. This study uses the ReMOT Control technique in Culex pipiens pallens (L.) to produce genetically modified mosquitoes.



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    Evident Corporation bx4 epifluorescence microscope
    A.1 Vagal motor efferent fibers (red; arrow head) were labeled using fluorescence conjugated streptavidin on 5 µm thin coronal section of small bowel. Labeled vagus fibers were found between circular and longitudinal muscle layers at the level of the myenteric plexus. A.2. High power magnification field showing localization of vagal motor efferent fibers (red, arrow head) between nuclei (blue) of circular (CM) and longitudinal (LM) smooth muscle. A.3. The presence of intrinsic biotin was found in cells of the submucosal crypts. B. Labeled-fibers of the vagal nerve were revealed with ABC/DAB staining protocol while cuprolinic blue was used as pan-neuronal marker to visualize enteric neurons (blue). Labeled vagal efferent fibers and terminals with a basket-like shape terminals were found within myenteric ganglia (arrow head). C. Confocal image showing the presence of the dextran amine in the inter-ganglionic fibers (arrow). D. <t>Epifluorescence</t> image corresponding to vagal efferent fibers (green) densely found at the level of myenteric ganglion (PGP 9.5, red). The scale bar represents 50 µm.
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    A.1 Vagal motor efferent fibers (red; arrow head) were labeled using fluorescence conjugated streptavidin on 5 µm thin coronal section of small bowel. Labeled vagus fibers were found between circular and longitudinal muscle layers at the level of the myenteric plexus. A.2. High power magnification field showing localization of vagal motor efferent fibers (red, arrow head) between nuclei (blue) of circular (CM) and longitudinal (LM) smooth muscle. A.3. The presence of intrinsic biotin was found in cells of the submucosal crypts. B. Labeled-fibers of the vagal nerve were revealed with ABC/DAB staining protocol while cuprolinic blue was used as pan-neuronal marker to visualize enteric neurons (blue). Labeled vagal efferent fibers and terminals with a basket-like shape terminals were found within myenteric ganglia (arrow head). C. Confocal image showing the presence of the dextran amine in the inter-ganglionic fibers (arrow). D. <t>Epifluorescence</t> image corresponding to vagal efferent fibers (green) densely found at the level of myenteric ganglion (PGP 9.5, red). The scale bar represents 50 µm.
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    Image Search Results


    A.1 Vagal motor efferent fibers (red; arrow head) were labeled using fluorescence conjugated streptavidin on 5 µm thin coronal section of small bowel. Labeled vagus fibers were found between circular and longitudinal muscle layers at the level of the myenteric plexus. A.2. High power magnification field showing localization of vagal motor efferent fibers (red, arrow head) between nuclei (blue) of circular (CM) and longitudinal (LM) smooth muscle. A.3. The presence of intrinsic biotin was found in cells of the submucosal crypts. B. Labeled-fibers of the vagal nerve were revealed with ABC/DAB staining protocol while cuprolinic blue was used as pan-neuronal marker to visualize enteric neurons (blue). Labeled vagal efferent fibers and terminals with a basket-like shape terminals were found within myenteric ganglia (arrow head). C. Confocal image showing the presence of the dextran amine in the inter-ganglionic fibers (arrow). D. Epifluorescence image corresponding to vagal efferent fibers (green) densely found at the level of myenteric ganglion (PGP 9.5, red). The scale bar represents 50 µm.

    Journal: PLoS ONE

    Article Title: Neuro-Anatomical Evidence Indicating Indirect Modulation of Macrophages by Vagal Efferents in the Intestine but Not in the Spleen

    doi: 10.1371/journal.pone.0087785

    Figure Lengend Snippet: A.1 Vagal motor efferent fibers (red; arrow head) were labeled using fluorescence conjugated streptavidin on 5 µm thin coronal section of small bowel. Labeled vagus fibers were found between circular and longitudinal muscle layers at the level of the myenteric plexus. A.2. High power magnification field showing localization of vagal motor efferent fibers (red, arrow head) between nuclei (blue) of circular (CM) and longitudinal (LM) smooth muscle. A.3. The presence of intrinsic biotin was found in cells of the submucosal crypts. B. Labeled-fibers of the vagal nerve were revealed with ABC/DAB staining protocol while cuprolinic blue was used as pan-neuronal marker to visualize enteric neurons (blue). Labeled vagal efferent fibers and terminals with a basket-like shape terminals were found within myenteric ganglia (arrow head). C. Confocal image showing the presence of the dextran amine in the inter-ganglionic fibers (arrow). D. Epifluorescence image corresponding to vagal efferent fibers (green) densely found at the level of myenteric ganglion (PGP 9.5, red). The scale bar represents 50 µm.

    Article Snippet: Preparations were examined by use of an Olympus BX4 epifluorescence microscope (Olympus America, Center Valley, PA).

    Techniques: Labeling, Fluorescence, Staining, Marker

    Epifluorescence images collected for the identification of the neurotransmitters (red) and dextran-labeled vagus efferent fibers and terminals (Green). Choline acetylfransferase (ChAT, A), neuronal nitric oxide synthase (nNOS, B), Tyrosine hydroxylase (TH, C), substance P (SP, D), vasoactive intestinal peptide (VIP, E) and Calcitonin gene related peptide (CGRP, F). Arrow heads point discrete co-localization between Vagus nerve and VIP or CGRP positive structures. Vagus nerve efferent fibers and terminals are only positive for ChAT and located in close proximity to ChAT and nNOS enteric neuronal bodies. Scale bars represent 20 µm.

    Journal: PLoS ONE

    Article Title: Neuro-Anatomical Evidence Indicating Indirect Modulation of Macrophages by Vagal Efferents in the Intestine but Not in the Spleen

    doi: 10.1371/journal.pone.0087785

    Figure Lengend Snippet: Epifluorescence images collected for the identification of the neurotransmitters (red) and dextran-labeled vagus efferent fibers and terminals (Green). Choline acetylfransferase (ChAT, A), neuronal nitric oxide synthase (nNOS, B), Tyrosine hydroxylase (TH, C), substance P (SP, D), vasoactive intestinal peptide (VIP, E) and Calcitonin gene related peptide (CGRP, F). Arrow heads point discrete co-localization between Vagus nerve and VIP or CGRP positive structures. Vagus nerve efferent fibers and terminals are only positive for ChAT and located in close proximity to ChAT and nNOS enteric neuronal bodies. Scale bars represent 20 µm.

    Article Snippet: Preparations were examined by use of an Olympus BX4 epifluorescence microscope (Olympus America, Center Valley, PA).

    Techniques: Labeling

    A. Staining of F4/80 positive intestinal resident macrophages (brown) surrounding a myenteric ganglion (blue). Efferent vagus nerve fibers are shown in black. B.1 Regular distribution of resident macrophages (F4/80) in the muscularis of the murine small bowel. B.2 & C. Confocal image showing the distribution of the resident macrophage (F4/80, blue) close to enteric neurons (PGP9.5, red) in the muscle layers of the small intestine. D. Epifluorescence image showing the presence of resident macrophages (F4/80, blue) in close proximity to ChAT positive enteric ganglion (red). Scale bar represents 25 µm, except for B.1 it represents 0.1 mm.

    Journal: PLoS ONE

    Article Title: Neuro-Anatomical Evidence Indicating Indirect Modulation of Macrophages by Vagal Efferents in the Intestine but Not in the Spleen

    doi: 10.1371/journal.pone.0087785

    Figure Lengend Snippet: A. Staining of F4/80 positive intestinal resident macrophages (brown) surrounding a myenteric ganglion (blue). Efferent vagus nerve fibers are shown in black. B.1 Regular distribution of resident macrophages (F4/80) in the muscularis of the murine small bowel. B.2 & C. Confocal image showing the distribution of the resident macrophage (F4/80, blue) close to enteric neurons (PGP9.5, red) in the muscle layers of the small intestine. D. Epifluorescence image showing the presence of resident macrophages (F4/80, blue) in close proximity to ChAT positive enteric ganglion (red). Scale bar represents 25 µm, except for B.1 it represents 0.1 mm.

    Article Snippet: Preparations were examined by use of an Olympus BX4 epifluorescence microscope (Olympus America, Center Valley, PA).

    Techniques: Staining

    A. Epifluorescence image shows dextran-labeled vagal efferents (green) that co-localize with ChaT (yellow), and are in close contact with ChaT positive enteric neurons (red). B. Epifluorescence image shows labeled vagal efferent fibers (green) making contact with nNOS positive neurons (red). Of note, cholinergic neurons, and to lesser extent nitrergic neurons, are the main population targeted by the vagal efferent fibers. C. Confocal image of VIP (red) and nNOS (green) myenteric neurons. Most of the cells bodies exhibit co-localization of these two neurotransmitters (arrow head). D. Confocal image of VIP (red) and ChaT (green) myenteric neurons. Occasionally myenteric neurons showed immunoreactivity for both neurotransmitters (arrow head). C1 and C2 show the distribution for the nNOS and VIP positive cells bodies, respectively. D1 and D2 show the distribution for ChaT and VIP positive cells bodies. Scale bar represents 20 µm.

    Journal: PLoS ONE

    Article Title: Neuro-Anatomical Evidence Indicating Indirect Modulation of Macrophages by Vagal Efferents in the Intestine but Not in the Spleen

    doi: 10.1371/journal.pone.0087785

    Figure Lengend Snippet: A. Epifluorescence image shows dextran-labeled vagal efferents (green) that co-localize with ChaT (yellow), and are in close contact with ChaT positive enteric neurons (red). B. Epifluorescence image shows labeled vagal efferent fibers (green) making contact with nNOS positive neurons (red). Of note, cholinergic neurons, and to lesser extent nitrergic neurons, are the main population targeted by the vagal efferent fibers. C. Confocal image of VIP (red) and nNOS (green) myenteric neurons. Most of the cells bodies exhibit co-localization of these two neurotransmitters (arrow head). D. Confocal image of VIP (red) and ChaT (green) myenteric neurons. Occasionally myenteric neurons showed immunoreactivity for both neurotransmitters (arrow head). C1 and C2 show the distribution for the nNOS and VIP positive cells bodies, respectively. D1 and D2 show the distribution for ChaT and VIP positive cells bodies. Scale bar represents 20 µm.

    Article Snippet: Preparations were examined by use of an Olympus BX4 epifluorescence microscope (Olympus America, Center Valley, PA).

    Techniques: Labeling

    Epifluorescence images show F4/80 positive intestinal resident macrophages (blue) located in close proximity to inter-ganglionic enteric fibers positive for ChAT (A), nNOS (B) and VIP (C). D. Intestinal resident macrophages (F4/80, red, D.1) expressing α7 nicotinic receptor (green, arrow heads, D.2). E. Resident macrophages of the gut muscularis (F4/80, red) express VPAC1 receptors (green). Asterisk corresponds to intestinal resident macrophages located at the level of the myenteric plexus region. The other macrophage is located at the level of the submucosal plexus. Scale bar represents 10 µm from A–C and 20 µm from D–E.

    Journal: PLoS ONE

    Article Title: Neuro-Anatomical Evidence Indicating Indirect Modulation of Macrophages by Vagal Efferents in the Intestine but Not in the Spleen

    doi: 10.1371/journal.pone.0087785

    Figure Lengend Snippet: Epifluorescence images show F4/80 positive intestinal resident macrophages (blue) located in close proximity to inter-ganglionic enteric fibers positive for ChAT (A), nNOS (B) and VIP (C). D. Intestinal resident macrophages (F4/80, red, D.1) expressing α7 nicotinic receptor (green, arrow heads, D.2). E. Resident macrophages of the gut muscularis (F4/80, red) express VPAC1 receptors (green). Asterisk corresponds to intestinal resident macrophages located at the level of the myenteric plexus region. The other macrophage is located at the level of the submucosal plexus. Scale bar represents 10 µm from A–C and 20 µm from D–E.

    Article Snippet: Preparations were examined by use of an Olympus BX4 epifluorescence microscope (Olympus America, Center Valley, PA).

    Techniques: Expressing