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  • 85
    Toronto Research Chemicals isosorbide dinitrate
    Isosorbide Dinitrate, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc cx43
    Cx43, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC momlv gag pol
    Momlv Gag Pol, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ProSci Incorporated ace2
    Histologic and molecular correlates of COVID-19 in human brains. Panel A shows the microvessels in normal brain. In comparison, many of the capillaries in COVID-19 brain tissues show marked perivascular edema (panel B). Serial section analyses of the COVID-19 brain shows that the endothelial cells of the microvessels contained the spike glycoprotein (panel C), the <t>ACE2</t> receptor (panel D) and IL 6 (panel F), but not viral RNA (panel E). The fluorescent yellow signal marks co-localization of the spike protein with IL6 (panel G) and caspase 3 (panel H), respectively, in these endothelial cells. Each magnification is 800× with DAB (brown) signal (panels C, E, F) or Fast Red (red) (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Ace2, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biosynth Carbosynth fluorogenic substrate benzyloxycarbonyl l histidyl l glutamyl l lysine 4 methyl coumaryl 7 amide
    Histologic and molecular correlates of COVID-19 in human brains. Panel A shows the microvessels in normal brain. In comparison, many of the capillaries in COVID-19 brain tissues show marked perivascular edema (panel B). Serial section analyses of the COVID-19 brain shows that the endothelial cells of the microvessels contained the spike glycoprotein (panel C), the <t>ACE2</t> receptor (panel D) and IL 6 (panel F), but not viral RNA (panel E). The fluorescent yellow signal marks co-localization of the spike protein with IL6 (panel G) and caspase 3 (panel H), respectively, in these endothelial cells. Each magnification is 800× with DAB (brown) signal (panels C, E, F) or Fast Red (red) (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Fluorogenic Substrate Benzyloxycarbonyl L Histidyl L Glutamyl L Lysine 4 Methyl Coumaryl 7 Amide, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Histologic and molecular correlates of COVID-19 in human brains. Panel A shows the microvessels in normal brain. In comparison, many of the capillaries in COVID-19 brain tissues show marked perivascular edema (panel B). Serial section analyses of the COVID-19 brain shows that the endothelial cells of the microvessels contained the spike glycoprotein (panel C), the ACE2 receptor (panel D) and IL 6 (panel F), but not viral RNA (panel E). The fluorescent yellow signal marks co-localization of the spike protein with IL6 (panel G) and caspase 3 (panel H), respectively, in these endothelial cells. Each magnification is 800× with DAB (brown) signal (panels C, E, F) or Fast Red (red) (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Journal: Annals of Diagnostic Pathology

    Article Title: Endothelial cell damage is the central part of COVID-19 and a mouse model induced by injection of the S1 subunit of the spike protein

    doi: 10.1016/j.anndiagpath.2020.151682

    Figure Lengend Snippet: Histologic and molecular correlates of COVID-19 in human brains. Panel A shows the microvessels in normal brain. In comparison, many of the capillaries in COVID-19 brain tissues show marked perivascular edema (panel B). Serial section analyses of the COVID-19 brain shows that the endothelial cells of the microvessels contained the spike glycoprotein (panel C), the ACE2 receptor (panel D) and IL 6 (panel F), but not viral RNA (panel E). The fluorescent yellow signal marks co-localization of the spike protein with IL6 (panel G) and caspase 3 (panel H), respectively, in these endothelial cells. Each magnification is 800× with DAB (brown) signal (panels C, E, F) or Fast Red (red) (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: The antibodies used follow; ABCAM, Cambridge MA (IL6, TNFα, NMDAR2, SHIP1, caspase 3, and C5b-9), Enzo Life Sciences (neuronal NOS, MFSD2a), ACE2 (PROSCI, Poway CA) (cat # 3215) and optimal pretreatment in each case was 30 min with the Leica EDTA antigen retrieval solution.

    Techniques:

    Quantification of cell line data after incubation with different subunits of the SARS-CoV2 spike protein.

    Journal: Annals of Diagnostic Pathology

    Article Title: Endothelial cell damage is the central part of COVID-19 and a mouse model induced by injection of the S1 subunit of the spike protein

    doi: 10.1016/j.anndiagpath.2020.151682

    Figure Lengend Snippet: Quantification of cell line data after incubation with different subunits of the SARS-CoV2 spike protein.

    Article Snippet: The antibodies used follow; ABCAM, Cambridge MA (IL6, TNFα, NMDAR2, SHIP1, caspase 3, and C5b-9), Enzo Life Sciences (neuronal NOS, MFSD2a), ACE2 (PROSCI, Poway CA) (cat # 3215) and optimal pretreatment in each case was 30 min with the Leica EDTA antigen retrieval solution.

    Techniques: Incubation

    Cytologic and molecular correlates of the S1 subunit of the spike protein in cell lines. Panel A shows the cytology of untreated HUVEC cells; these endothelial cells strongly express ACE2 (panel B). Treatment with the S1 subunit of spike protein induced cell aggregation and degeneration (panel C). The S1 subunit was not endocytosed by the RAW cells (panel D) and was evident in the HUVEC cells where it co-localized with caspase 3 as seen in panels F-H. Panel F is the isolated spike data (fluorescent green), panel G the isolated caspase 3 data (fluorescent red) and panel H the merged image with fluorescent yellow marking the co-localization of the two protein. The MN cells likewise showed co-localization of the spike protein and caspase 3 (panel E). The magnifications are 600× (panels A-D) and 1000× (panels E -F) with DAB (brown) signal (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Journal: Annals of Diagnostic Pathology

    Article Title: Endothelial cell damage is the central part of COVID-19 and a mouse model induced by injection of the S1 subunit of the spike protein

    doi: 10.1016/j.anndiagpath.2020.151682

    Figure Lengend Snippet: Cytologic and molecular correlates of the S1 subunit of the spike protein in cell lines. Panel A shows the cytology of untreated HUVEC cells; these endothelial cells strongly express ACE2 (panel B). Treatment with the S1 subunit of spike protein induced cell aggregation and degeneration (panel C). The S1 subunit was not endocytosed by the RAW cells (panel D) and was evident in the HUVEC cells where it co-localized with caspase 3 as seen in panels F-H. Panel F is the isolated spike data (fluorescent green), panel G the isolated caspase 3 data (fluorescent red) and panel H the merged image with fluorescent yellow marking the co-localization of the two protein. The MN cells likewise showed co-localization of the spike protein and caspase 3 (panel E). The magnifications are 600× (panels A-D) and 1000× (panels E -F) with DAB (brown) signal (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: The antibodies used follow; ABCAM, Cambridge MA (IL6, TNFα, NMDAR2, SHIP1, caspase 3, and C5b-9), Enzo Life Sciences (neuronal NOS, MFSD2a), ACE2 (PROSCI, Poway CA) (cat # 3215) and optimal pretreatment in each case was 30 min with the Leica EDTA antigen retrieval solution.

    Techniques: Isolation