begm medium Search Results


bronchial epithelial cell growth medium (begm)  (MultiCell Technologies)
90
MultiCell Technologies bronchial epithelial cell growth medium (begm)
Bronchial Epithelial Cell Growth Medium (Begm), supplied by MultiCell Technologies, 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/begm+medium/bronchial+epithelial+cell+growth+medium++begm+/us11279719-1001-5-15
Average 90 stars, based on 1 article reviews
bronchial epithelial cell growth medium (begm) - by Bioz Stars, 2026-09
90/100 stars
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bronchial epithelial growth medium (begm)  (Biowhittaker Inc)
90
Biowhittaker Inc bronchial epithelial growth medium (begm)
Bronchial Epithelial Growth Medium (Begm), supplied by Biowhittaker 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/begm+medium/bronchial+epithelial+growth+medium++begm+/pmc03496160-164-13-21
Average 90 stars, based on 1 article reviews
bronchial epithelial growth medium (begm) - by Bioz Stars, 2026-09
90/100 stars
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growth medium pneumacult-ex media; begm  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc growth medium pneumacult-ex media; begm
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Growth Medium Pneumacult Ex Media; Begm, supplied by STEMCELL Technologies 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/begm+medium/growth+medium+pneumacult+ex+media++begm/pmc10155187-266-2-15
Average 90 stars, based on 1 article reviews
growth medium pneumacult-ex media; begm - by Bioz Stars, 2026-09
90/100 stars
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bronchial epithelial growth medium begm cc-3170  (BioWhittaker Molecular Applications)
90
BioWhittaker Molecular Applications bronchial epithelial growth medium begm cc-3170
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Bronchial Epithelial Growth Medium Begm Cc 3170, supplied by BioWhittaker Molecular Applications, 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/begm+medium/bronchial+epithelial+growth+medium+begm/pm32643865-33-8-14
Average 90 stars, based on 1 article reviews
bronchial epithelial growth medium begm cc-3170 - by Bioz Stars, 2026-09
90/100 stars
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begm medium  (Biowhittaker Inc)
90
Biowhittaker Inc begm medium
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Begm Medium, supplied by Biowhittaker 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/begm+medium/begm+medium/pm21706049-179-5-7
Average 90 stars, based on 1 article reviews
begm medium - by Bioz Stars, 2026-09
90/100 stars
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begm-corning sf test medium  (Corning Life Sciences)
90
Corning Life Sciences begm-corning sf test medium
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Begm Corning Sf Test Medium, supplied by Corning Life Sciences, 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/begm+medium/begm+corning+sf+test+medium/pmc06105780-197-12-12
Average 90 stars, based on 1 article reviews
begm-corning sf test medium - by Bioz Stars, 2026-09
90/100 stars
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bronchial epithelial growth medium begm  (Beijing Sunbio Biotech Co)
90
Beijing Sunbio Biotech Co bronchial epithelial growth medium begm
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Bronchial Epithelial Growth Medium Begm, supplied by Beijing Sunbio Biotech Co, 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/begm+medium/bronchial+epithelial+growth+medium+begm/pm35583012-16-19-25
Average 90 stars, based on 1 article reviews
bronchial epithelial growth medium begm - by Bioz Stars, 2026-09
90/100 stars
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begm medium  (Corning Life Sciences)
90
Corning Life Sciences begm medium
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Begm Medium, supplied by Corning Life Sciences, 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/begm+medium/begm+medium/pmc05404321-47-21-34
Average 90 stars, based on 1 article reviews
begm medium - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
begm medium  (BioWhittaker Molecular Applications)
90
BioWhittaker Molecular Applications begm medium
Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary <t>NHBE</t> cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid <t>interface</t> <t>(ALI)</t> culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).
Begm Medium, supplied by BioWhittaker Molecular Applications, 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/begm+medium/begm+medium/pm12676864-57-13-15
Average 90 stars, based on 1 article reviews
begm medium - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

Image Search Results


Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary NHBE cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid interface (ALI) culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).

Journal: Cell and tissue research

Article Title: Transcriptomic and Ultrastructural Evidence Indicate That Anti-HMGB1 Antibodies Rescue Organic Dust Induced Mitochondrial Dysfunction

doi: 10.1007/s00441-022-03602-3

Figure Lengend Snippet: Three experimental designs were used to study the impact of HMGB1 on mitochondria during ODE exposure. For acute exposure, primary NHBE cells were transfected with HMGB1 targeted siRNA to induce knockdown followed by exposure to either media (control) or ODE (1%) for 24 h (a). For chronic exposure, NHBE cells were treated with media alone (control) or ODE (1%) followed by media (control) or HMGB1 neutralization antibody (10 μg/mL) for 8 h per day for five days (b). Air-liquid interface (ALI) culture model was developed by seeing NHBE cells onto a semi-permeable membrane to develop and the differentiated cells were exposed to ODE, with or without HMGB1 neutralization for 1 h per day for 5 days (c).

Article Snippet: We purchased NHBE – growth medium (Pneumacult-Ex media; BEGM) and differentiation media (Pneumacult-ALI media) from StemCell Technologies.

Techniques: Transfection, Knockdown, Control, Neutralization, Membrane

NHBE cells differentiated on air-liquid interface (ALI) culture treated with medium or ODE (1%) followed by medium or HMGB1 neutralization antibody (10 μg/mL) for 1 h per day for 5 days. mRNA fold change of markers of motile cilia, foxj1 (a) and cfap157 (b), and tight junction, ocln (c) and cldn 1 (d), was measured by qPCR. Tight junction integrity was assessed by trans-epithelial electrical resistance (TEER) measurement (e). Samples for all assays were derived from the same experiment and were processed in parallel. Data was analyzed using one-way ANOVA with Tukey’s multiple comparison test (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001) and represented as mean ± SEM with n = 3/treatment (* indicates significant difference from control).

Journal: Cell and tissue research

Article Title: Transcriptomic and Ultrastructural Evidence Indicate That Anti-HMGB1 Antibodies Rescue Organic Dust Induced Mitochondrial Dysfunction

doi: 10.1007/s00441-022-03602-3

Figure Lengend Snippet: NHBE cells differentiated on air-liquid interface (ALI) culture treated with medium or ODE (1%) followed by medium or HMGB1 neutralization antibody (10 μg/mL) for 1 h per day for 5 days. mRNA fold change of markers of motile cilia, foxj1 (a) and cfap157 (b), and tight junction, ocln (c) and cldn 1 (d), was measured by qPCR. Tight junction integrity was assessed by trans-epithelial electrical resistance (TEER) measurement (e). Samples for all assays were derived from the same experiment and were processed in parallel. Data was analyzed using one-way ANOVA with Tukey’s multiple comparison test (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001) and represented as mean ± SEM with n = 3/treatment (* indicates significant difference from control).

Article Snippet: We purchased NHBE – growth medium (Pneumacult-Ex media; BEGM) and differentiation media (Pneumacult-ALI media) from StemCell Technologies.

Techniques: Neutralization, Derivative Assay, Comparison, Control