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pet 15b lfn dta  (Addgene inc)


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    Structured Review

    Addgene inc pet 15b lfn dta
    Pet 15b Lfn Dta, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pet 15b lfn dta/product/Addgene inc
    Average 92 stars, based on 10 article reviews
    pet 15b lfn dta - by Bioz Stars, 2026-06
    92/100 stars

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    Novus Biologicals alpha smooth muscle actin
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    The Endothelin-1 (ET-1) Pathway Demonstrates Heightened Expression in Both the Plasma and Lung Microvessels of Chronic Thromboembolic Pulmonary Hypertension (CTEPH) Patients. (A) The concentration of ET-1 in venous plasma is elevated in CTEPH patients (n = 59) compared to control subjects (n = 41). (B) Co-immunofluorescent staining for ET-1 (red), von Willebrand factor (vWF, white), alpha-smooth muscle actin (α-SMA, green), and DAPI (blue) within lung microvessels from control subjects, CTEPH patients, and idiopathic pulmonary arterial hypertension (iPAH) patients, and the quantification of ET-1 fluorescent mean intensity (FMI) in the pulmonary endothelium (n = 5). (C) Co-immunofluorescent staining for ET-1 receptor A (ET A ) (red), α-SMA (green), and DAPI (blue) in controls, CTEPH, and iPAH lungs, along with quantification of ET A FMI in pulmonary artery smooth muscle cells (PA-SMCs) (n = 5). (D) Co-immunofluorescent staining for phospho-myosin light chain (p-MLC) (red), α-SMA (green), and DAPI (blue) in controls, CTEPH, and iPAH lungs, along with quantification of p-MLC FMI in PA-SMCs (n = 5). All data are presented as mean with standard error of the mean (SEM). Statistical significance is denoted as * for P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001 and “ns” for not significant. The scale bar in all staining images is set at 100 µm.

    Journal: Scientific Reports

    Article Title: Exploring the Endothelin-1 pathway in chronic thromboembolic pulmonary hypertension microvasculopathy

    doi: 10.1038/s41598-024-79623-5

    Figure Lengend Snippet: The Endothelin-1 (ET-1) Pathway Demonstrates Heightened Expression in Both the Plasma and Lung Microvessels of Chronic Thromboembolic Pulmonary Hypertension (CTEPH) Patients. (A) The concentration of ET-1 in venous plasma is elevated in CTEPH patients (n = 59) compared to control subjects (n = 41). (B) Co-immunofluorescent staining for ET-1 (red), von Willebrand factor (vWF, white), alpha-smooth muscle actin (α-SMA, green), and DAPI (blue) within lung microvessels from control subjects, CTEPH patients, and idiopathic pulmonary arterial hypertension (iPAH) patients, and the quantification of ET-1 fluorescent mean intensity (FMI) in the pulmonary endothelium (n = 5). (C) Co-immunofluorescent staining for ET-1 receptor A (ET A ) (red), α-SMA (green), and DAPI (blue) in controls, CTEPH, and iPAH lungs, along with quantification of ET A FMI in pulmonary artery smooth muscle cells (PA-SMCs) (n = 5). (D) Co-immunofluorescent staining for phospho-myosin light chain (p-MLC) (red), α-SMA (green), and DAPI (blue) in controls, CTEPH, and iPAH lungs, along with quantification of p-MLC FMI in PA-SMCs (n = 5). All data are presented as mean with standard error of the mean (SEM). Statistical significance is denoted as * for P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001 and “ns” for not significant. The scale bar in all staining images is set at 100 µm.

    Article Snippet: Immunofluorescent staining for ET-1 (Abcam for human lung staining, Abcam and Origen for piglet lung staining), ET A (Novus Biologicals for human staining, Abcam for piglet model staining), phosphorylated MLC (Cell signaling), alpha-smooth muscle actin (α-SMA, Novus Biologicals) were performed in human and piglet lung paraffin sections.

    Techniques: Expressing, Clinical Proteomics, Concentration Assay, Control, Staining

    The Endothelin-1 (ET-1) Pathway Demonstrates Increased Expression in both the Plasma and Lung Microvessels of the CTEPH Piglet Model. (A) The concentration of ET-1 in venous plasma in the CTEPH piglet model compared to sham controls (n = 11). (B) Co-immunofluorescent staining for ET-1 (red), von Willebrand factor (vWF, white), alpha-smooth muscle actin (α-SMA, green), and DAPI (blue) within lung microvessels from the sham controls, non-obstructed (RSL), and obstructed (LSL) territories, along with quantification of fluorescent mean intensity (FMI) in the pulmonary endothelium (n = 5). (C) Co-immunofluorescent staining for ET-1 receptor A (ET A ) (red), a-SMA (green), and DAPI (blue) in sham lungs, and the RSL and LSL territories, along with quantification of FMI in pulmonary artery smooth muscle cells (PA-SMCs) (n = 5). (D) Co-immunofluorescent staining for phospho-myosin light chain (p-MLC) (red), α-SMA (green), and DAPI (blue) in sham lungs, and the RSL and LSL territories, along with quantification of FMI in PA- SMCs (n = 5). All data are presented as mean values with standard error of the mean (SEM). Statistical significance is denoted as * for P < 0.05, ** P < 0.01, and *** P < 0.001. The scale bar in all staining images is set at 100 µm. LSL: left superior lobe; RSL: right superior lobe.

    Journal: Scientific Reports

    Article Title: Exploring the Endothelin-1 pathway in chronic thromboembolic pulmonary hypertension microvasculopathy

    doi: 10.1038/s41598-024-79623-5

    Figure Lengend Snippet: The Endothelin-1 (ET-1) Pathway Demonstrates Increased Expression in both the Plasma and Lung Microvessels of the CTEPH Piglet Model. (A) The concentration of ET-1 in venous plasma in the CTEPH piglet model compared to sham controls (n = 11). (B) Co-immunofluorescent staining for ET-1 (red), von Willebrand factor (vWF, white), alpha-smooth muscle actin (α-SMA, green), and DAPI (blue) within lung microvessels from the sham controls, non-obstructed (RSL), and obstructed (LSL) territories, along with quantification of fluorescent mean intensity (FMI) in the pulmonary endothelium (n = 5). (C) Co-immunofluorescent staining for ET-1 receptor A (ET A ) (red), a-SMA (green), and DAPI (blue) in sham lungs, and the RSL and LSL territories, along with quantification of FMI in pulmonary artery smooth muscle cells (PA-SMCs) (n = 5). (D) Co-immunofluorescent staining for phospho-myosin light chain (p-MLC) (red), α-SMA (green), and DAPI (blue) in sham lungs, and the RSL and LSL territories, along with quantification of FMI in PA- SMCs (n = 5). All data are presented as mean values with standard error of the mean (SEM). Statistical significance is denoted as * for P < 0.05, ** P < 0.01, and *** P < 0.001. The scale bar in all staining images is set at 100 µm. LSL: left superior lobe; RSL: right superior lobe.

    Article Snippet: Immunofluorescent staining for ET-1 (Abcam for human lung staining, Abcam and Origen for piglet lung staining), ET A (Novus Biologicals for human staining, Abcam for piglet model staining), phosphorylated MLC (Cell signaling), alpha-smooth muscle actin (α-SMA, Novus Biologicals) were performed in human and piglet lung paraffin sections.

    Techniques: Expressing, Clinical Proteomics, Concentration Assay, Staining