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rat pulmonary artery endothelial cells (rpaecs)  (Procell Inc)

 
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    Structured Review

    Procell Inc rat pulmonary artery endothelial cells (rpaecs)
    Rat Pulmonary Artery Endothelial Cells (Rpaecs), supplied by Procell Inc, 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/rat+pulmonary+artery+endothelial+cells+(rpaecs)/rat+pulmonary+microvascular+endothelial+cells++pmvecs+/pm40427635-193-0-39
    Average 90 stars, based on 1 article reviews
    rat pulmonary artery endothelial cells (rpaecs) - by Bioz Stars, 2026-10
    90/100 stars

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    Fluorescence:

    Article Title: Iron Replacement Attenuates Hypoxic Pulmonary Hypertension by Remodeling Energy Metabolism via Regulating the HIF2α/Mitochondrial Complex I, III/ROS Axis
    Article Snippet: The kit for iron measurement was from Nanjing Jiancheng Bioengineering Institute, China (Cat. # A039-1-1; A039-2-1), and the kit for ferritin measurement was from Elabscience Biotechnology Co., Ltd. (Wuhan, China) (Cat. # E-EL-R3018). .. Rat pulmonary artery endothelial cells (RPAECs, CD31 fluorescence identification is reported in ) and human pulmonary artery endothelial cells (HPAECs, the short tandem repeat (STR) assay report is shown in ) were supplied by Wuhan Procell Life Technology Co., Ltd., (Wuhan, China) and Bena Biological Technology Co., Ltd. (Xinyang, China)., respectively, and cultured with endothelial cell medium (ECM, ScienCell Research Laboratories, CA, USA) containing vascular endothelial growth factor at 37 °C with 5% CO 2 . ..

    Article Title: Iron Replacement Attenuates Hypoxic Pulmonary Hypertension by Remodeling Energy Metabolism via Regulating the HIF2α/Mitochondrial Complex I, III/ROS Axis.
    Article Snippet: The kit for iron measurement was from Nanjing Jiancheng Bioengineering Institute, China (Cat. # A039-1-1; A039-2-1), and the kit for ferritin measurement was from Elabscience Biotechnology Co., Ltd. (Wuhan, China) (Cat. # E-EL-R3018). .. Rat pulmonary artery endothelial cells (RPAECs, CD31 fluorescence identification is reported in Supplementary Figure S1F) and human pulmonary artery endothelial cells (HPAECs, the short tandem repeat (STR) assay report is shown in Supplementary Figure S1G,H) were supplied by Wuhan Procell Life Technology Co., Ltd., (Wuhan, China) and Bena Biological Technology Co., Ltd. (Xinyang, China)., respectively, and cultured with endothelial cell medium (ECM, ScienCell Research Laboratories, CA, USA) containing vascular endothelial growth factor at 37 ◦C with 5% CO2. ..

    Cell Culture:

    Article Title: Iron Replacement Attenuates Hypoxic Pulmonary Hypertension by Remodeling Energy Metabolism via Regulating the HIF2α/Mitochondrial Complex I, III/ROS Axis
    Article Snippet: The kit for iron measurement was from Nanjing Jiancheng Bioengineering Institute, China (Cat. # A039-1-1; A039-2-1), and the kit for ferritin measurement was from Elabscience Biotechnology Co., Ltd. (Wuhan, China) (Cat. # E-EL-R3018). .. Rat pulmonary artery endothelial cells (RPAECs, CD31 fluorescence identification is reported in ) and human pulmonary artery endothelial cells (HPAECs, the short tandem repeat (STR) assay report is shown in ) were supplied by Wuhan Procell Life Technology Co., Ltd., (Wuhan, China) and Bena Biological Technology Co., Ltd. (Xinyang, China)., respectively, and cultured with endothelial cell medium (ECM, ScienCell Research Laboratories, CA, USA) containing vascular endothelial growth factor at 37 °C with 5% CO 2 . ..

    Article Title: Iron Replacement Attenuates Hypoxic Pulmonary Hypertension by Remodeling Energy Metabolism via Regulating the HIF2α/Mitochondrial Complex I, III/ROS Axis.
    Article Snippet: The kit for iron measurement was from Nanjing Jiancheng Bioengineering Institute, China (Cat. # A039-1-1; A039-2-1), and the kit for ferritin measurement was from Elabscience Biotechnology Co., Ltd. (Wuhan, China) (Cat. # E-EL-R3018). .. Rat pulmonary artery endothelial cells (RPAECs, CD31 fluorescence identification is reported in Supplementary Figure S1F) and human pulmonary artery endothelial cells (HPAECs, the short tandem repeat (STR) assay report is shown in Supplementary Figure S1G,H) were supplied by Wuhan Procell Life Technology Co., Ltd., (Wuhan, China) and Bena Biological Technology Co., Ltd. (Xinyang, China)., respectively, and cultured with endothelial cell medium (ECM, ScienCell Research Laboratories, CA, USA) containing vascular endothelial growth factor at 37 ◦C with 5% CO2. ..



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    Proliferative characteristics of bone marrow-derived EPC . EPC and <t>rPAEC</t> <t>were</t> <t>cultured</t> in the presence of 20% FCS in EBM-2 without further supplements (Figure 3A) or in EBM-2 containing bFGF (Figure 3B). Figure 3A shows the differential growth capacities of EPC and mature rPAEC in the presence of EBM-2 supplemented with 20% FCS. Figure 3B shows the proliferative kinetics of EPC cultured in EBM-2 supplemented with 0.5% FCS towards increasing concentrations of bFGF (100 ng/ml to 100 μg/ml). Cells were seeded in 96-well plates, grown for 24 h in culture medium, washed twice with HEPES/EDTA and treated with bFGF in EBM-2 medium containing 0.5% FCS for 48 h as indicated. Cells were incubated with MTT solution, lysed and the absorbance was read. MTT activity is expressed as Optical Density and represents mean ± SEM of five independent experiments, ** p < 0.01, * p < 0.05.
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    Proliferative characteristics of bone marrow-derived EPC . EPC and rPAEC were cultured in the presence of 20% FCS in EBM-2 without further supplements (Figure 3A) or in EBM-2 containing bFGF (Figure 3B). Figure 3A shows the differential growth capacities of EPC and mature rPAEC in the presence of EBM-2 supplemented with 20% FCS. Figure 3B shows the proliferative kinetics of EPC cultured in EBM-2 supplemented with 0.5% FCS towards increasing concentrations of bFGF (100 ng/ml to 100 μg/ml). Cells were seeded in 96-well plates, grown for 24 h in culture medium, washed twice with HEPES/EDTA and treated with bFGF in EBM-2 medium containing 0.5% FCS for 48 h as indicated. Cells were incubated with MTT solution, lysed and the absorbance was read. MTT activity is expressed as Optical Density and represents mean ± SEM of five independent experiments, ** p < 0.01, * p < 0.05.

    Journal: Respiratory Research

    Article Title: Peripheral infusion of rat bone marrow derived endothelial progenitor cells leads to homing in acute lung injury

    doi: 10.1186/1465-9921-8-50

    Figure Lengend Snippet: Proliferative characteristics of bone marrow-derived EPC . EPC and rPAEC were cultured in the presence of 20% FCS in EBM-2 without further supplements (Figure 3A) or in EBM-2 containing bFGF (Figure 3B). Figure 3A shows the differential growth capacities of EPC and mature rPAEC in the presence of EBM-2 supplemented with 20% FCS. Figure 3B shows the proliferative kinetics of EPC cultured in EBM-2 supplemented with 0.5% FCS towards increasing concentrations of bFGF (100 ng/ml to 100 μg/ml). Cells were seeded in 96-well plates, grown for 24 h in culture medium, washed twice with HEPES/EDTA and treated with bFGF in EBM-2 medium containing 0.5% FCS for 48 h as indicated. Cells were incubated with MTT solution, lysed and the absorbance was read. MTT activity is expressed as Optical Density and represents mean ± SEM of five independent experiments, ** p < 0.01, * p < 0.05.

    Article Snippet: Rat pulmonary artery endothelial cells (rPAEC) were cultured in endothelial culture medium (Promo Cell, Heidelberg, Germany) containing 10% FCS and 2% endothelial cell growth supplement (Promo Cell, Heidelberg, Germany), 1% penicillin/streptomycin solution (Sigma, St. Louis, MO) and kept in a humidified incubator at 37°C in 5% CO 2 . rPAEC were used between passages three and five for all experiments.

    Techniques: Derivative Assay, Cell Culture, Incubation, Activity Assay