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primary human bronchial epithelial cells primary normal human bronchial epithelial nhbe cells  (ATCC)


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    ATCC primary human bronchial epithelial cells primary normal human bronchial epithelial nhbe cells
    Primary Human Bronchial Epithelial Cells Primary Normal Human Bronchial Epithelial Nhbe Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 540 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+human+bronchial+epithelial+nhbe+cells/Primary+Prostate+Epithelial+Cells%3B+Normal%2C+Human/pm42097143-717-0-15
    Average 99 stars, based on 540 article reviews
    primary human bronchial epithelial cells primary normal human bronchial epithelial nhbe cells - by Bioz Stars, 2026-09
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    Cell Culture:

    Article Title: Antimicrobial mitochondrial reactive oxygen species induction by lung epithelial immunometabolic modulation
    Article Snippet: .. Normal human bronchial epithelial (NHBE) cells were purchased from American Type Culture Collection (ATCC, Manassas, VA) and cultured in airway epithelial cell basal medium supplemented with bronchial epithelial cell growth kit (ATCC, Manassas, VA). .. Normal human Type II alveolar epithelial Cells were purchased from AcceGen (Fairfield, New Jersey) and air-liquid interface cultured in poly-L-Lysine coated transwells with alveolar epithelial cell medium (ScienCell Research Laboratories, Carlsbad, CA) for 5 days.

    Article Title: Research review and transcriptomic insights into Benzalkonium chloride inhalation and disease association.
    Article Snippet: .. Normal human bronchial epithelial (NHBE) cells from the ATCC Corporation were cultured in Airway Epithelial Cell Basal Medium (American Type Culture Collection, VA, USA), supplemented with a Bronchial Epithelial Cell Growth Kit (ATCC, VA, USA), penicillin (100 units/mL), and streptomycin (100 μg/mL). ..

    Article Title: Antimicrobial mitochondrial reactive oxygen species induction by lung epithelial metabolic reprogramming
    Article Snippet: .. Normal human bronchial epithelial (NHBE) cells were purchased from American Type Culture Collection (ATCC, Manassas, VA) and cultured in airway epithelial cell basal medium supplemented with bronchial epithelial cell growth kit (ATCC, Manassas, VA). ..

    Article Title: Antimicrobial mitochondrial reactive oxygen species induction by lung epithelial immunometabolic modulation.
    Article Snippet: .. Normal human bronchial epithelial (NHBE) cells were purchased from American Type Culture Collection (ATCC, Manassas, VA) and cultured in airway epithelial cell basal medium supplemented with bronchial epithelial cell growth kit (ATCC, Manassas, VA). .. Normal human Type II alveolar epithelial Cells were purchased from AcceGen (Fairfield, New Jersey) and air-liquid interface cultured in poly-L-Lysine coated transwells with alveolar epithelial cell medium (ScienCell Research Laboratories, Carlsbad, CA) for 5 days.



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    (A) Schematic of the PhysioMimix® lung MPS co-culture system. <t>Epithelial</t> cells were seeded on the apical side of the Transwell® insert and human pulmonary microvascular endothelial cells (HPMVECs) on the basolateral side, under air–liquid interface (ALI) and dynamic flow conditions. (B) Representative H&E and Alcian blue-stained histological section of bronchial MPS co-culture after 14 days. Mucus is stained blue; endothelial cells are indicated by white arrows. Scale bar, 50 µm. (C) TEER measurements comparing epithelial monoculture, endothelial monoculture, and epithelial–endothelial co-culture over 14 days under ALI conditions. (D) TEER comparison of bronchial and alveolar co-cultures grown under static or dynamic flow MPS conditions over the 14-day ALI differentiation period. (E) Gene expression of Club cell (SCGB1A1) and Goblet cell (MUC5AC) markers in <t>NHBE</t> cells before culture (NHBE pellet) and after 14 days of differentiation in MPS co- culture. (F) Gene expression of alveolar markers - AT1 (AQP5) and AT2 (SFTPB) - in SAEC cells before culture (SAEC pellet) and after 14 days of MPS co-culture. (G) Immunofluorescence staining of bronchial MPS co-culture tissue for acetylated α-tubulin (yellow), mucus (MUC5AC, green), actin (phalloidin, red), and nuclei (Hoechst 33342, blue). Top row shows epithelial layer; bottom row shows endothelial layer. Scale bar, 100 µm. (H) Immunofluorescence staining of alveolar MPS co-culture tissue after 14 days of differentiation, showing surfactant (SFTPB, green), actin (phalloidin, magenta), and nuclei (Hoechst 33342, blue). Endothelial cells are marked with white arrows. Scale bar, 20 µm.
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    Image Search Results


    (A) Schematic of the PhysioMimix® lung MPS co-culture system. Epithelial cells were seeded on the apical side of the Transwell® insert and human pulmonary microvascular endothelial cells (HPMVECs) on the basolateral side, under air–liquid interface (ALI) and dynamic flow conditions. (B) Representative H&E and Alcian blue-stained histological section of bronchial MPS co-culture after 14 days. Mucus is stained blue; endothelial cells are indicated by white arrows. Scale bar, 50 µm. (C) TEER measurements comparing epithelial monoculture, endothelial monoculture, and epithelial–endothelial co-culture over 14 days under ALI conditions. (D) TEER comparison of bronchial and alveolar co-cultures grown under static or dynamic flow MPS conditions over the 14-day ALI differentiation period. (E) Gene expression of Club cell (SCGB1A1) and Goblet cell (MUC5AC) markers in NHBE cells before culture (NHBE pellet) and after 14 days of differentiation in MPS co- culture. (F) Gene expression of alveolar markers - AT1 (AQP5) and AT2 (SFTPB) - in SAEC cells before culture (SAEC pellet) and after 14 days of MPS co-culture. (G) Immunofluorescence staining of bronchial MPS co-culture tissue for acetylated α-tubulin (yellow), mucus (MUC5AC, green), actin (phalloidin, red), and nuclei (Hoechst 33342, blue). Top row shows epithelial layer; bottom row shows endothelial layer. Scale bar, 100 µm. (H) Immunofluorescence staining of alveolar MPS co-culture tissue after 14 days of differentiation, showing surfactant (SFTPB, green), actin (phalloidin, magenta), and nuclei (Hoechst 33342, blue). Endothelial cells are marked with white arrows. Scale bar, 20 µm.

    Journal: bioRxiv

    Article Title: Dynamic Culture Improves the Predictive Power of Bronchial and Alveolar Airway Models of SARS-CoV-2 Infection

    doi: 10.1101/2025.07.21.665885

    Figure Lengend Snippet: (A) Schematic of the PhysioMimix® lung MPS co-culture system. Epithelial cells were seeded on the apical side of the Transwell® insert and human pulmonary microvascular endothelial cells (HPMVECs) on the basolateral side, under air–liquid interface (ALI) and dynamic flow conditions. (B) Representative H&E and Alcian blue-stained histological section of bronchial MPS co-culture after 14 days. Mucus is stained blue; endothelial cells are indicated by white arrows. Scale bar, 50 µm. (C) TEER measurements comparing epithelial monoculture, endothelial monoculture, and epithelial–endothelial co-culture over 14 days under ALI conditions. (D) TEER comparison of bronchial and alveolar co-cultures grown under static or dynamic flow MPS conditions over the 14-day ALI differentiation period. (E) Gene expression of Club cell (SCGB1A1) and Goblet cell (MUC5AC) markers in NHBE cells before culture (NHBE pellet) and after 14 days of differentiation in MPS co- culture. (F) Gene expression of alveolar markers - AT1 (AQP5) and AT2 (SFTPB) - in SAEC cells before culture (SAEC pellet) and after 14 days of MPS co-culture. (G) Immunofluorescence staining of bronchial MPS co-culture tissue for acetylated α-tubulin (yellow), mucus (MUC5AC, green), actin (phalloidin, red), and nuclei (Hoechst 33342, blue). Top row shows epithelial layer; bottom row shows endothelial layer. Scale bar, 100 µm. (H) Immunofluorescence staining of alveolar MPS co-culture tissue after 14 days of differentiation, showing surfactant (SFTPB, green), actin (phalloidin, magenta), and nuclei (Hoechst 33342, blue). Endothelial cells are marked with white arrows. Scale bar, 20 µm.

    Article Snippet: Airway models were comprised of human pulmonary microvascular endothelial cells (HPMEC) (PromoCell, C-12281, lot.489Z024.1) and small airway epithelial cells (SAEC) (Lonza, CC-2547, lot.21TL214918) or normal human bronchial epithelial cells (NHBE) (Lonza, CC-2540, lot.21TL035497) for the alveolar and bronchial airway model, respectively.

    Techniques: Co-Culture Assay, Staining, Comparison, Gene Expression, Immunofluorescence