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humidified co2 incubator  (Proteintech)


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    Proteintech humidified co2 incubator
    Humidified Co2 Incubator, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/humidified+co2+incubator/C2+Fusion+Protein/pmc12930742-96-12-29
    Average 94 stars, based on 1 article reviews
    humidified co2 incubator - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Neutralization:

    Article Title: Granzyme A-producing type 1 innate lymphoid cells promote salivary secretion in the aged submandibular gland.
    Article Snippet: .. Cocultures were maintained in RPMI medium supplemented with 10% FBS in a humidified CO2 incubator for 12 h. For neutralization of GZMA secreted by ILC1s, an anti-GZMA antibody (11288-1-AP; Proteintech, Rosemont, IL, USA) or isotype control (910801; BioLegend) was applied in accordance with the protocol described previously (20). ..

    Article Title: Granzyme A-producing type 1 innate lymphoid cells promote salivary secretion in the aged submandibular gland
    Article Snippet: .. Cocultures were maintained in RPMI medium supplemented with 10% FBS in a humidified CO2 incubator for 12 h. For neutralization of GZMA secreted by ILC1s, an anti-GZMA antibody (11,288–1-AP; Proteintech, Rosemont, IL, USA) or isotype control (910,801; BioLegend) was applied in accordance with the protocol described previously [ ]. ..

    Control:

    Article Title: Granzyme A-producing type 1 innate lymphoid cells promote salivary secretion in the aged submandibular gland.
    Article Snippet: .. Cocultures were maintained in RPMI medium supplemented with 10% FBS in a humidified CO2 incubator for 12 h. For neutralization of GZMA secreted by ILC1s, an anti-GZMA antibody (11288-1-AP; Proteintech, Rosemont, IL, USA) or isotype control (910801; BioLegend) was applied in accordance with the protocol described previously (20). ..

    Article Title: Granzyme A-producing type 1 innate lymphoid cells promote salivary secretion in the aged submandibular gland
    Article Snippet: .. Cocultures were maintained in RPMI medium supplemented with 10% FBS in a humidified CO2 incubator for 12 h. For neutralization of GZMA secreted by ILC1s, an anti-GZMA antibody (11,288–1-AP; Proteintech, Rosemont, IL, USA) or isotype control (910,801; BioLegend) was applied in accordance with the protocol described previously [ ]. ..



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    Regulation of the cGMP–PKG pathway by representative active components of ONSMP in OGD-induced H9C2 cells. A Determination of optimal concentrations of Baicalin and Kaempferide by CCK-8 assay. B Effects of Baicalin and Kaempferide on OGD-induced H9C2 cell viability. C IHC analysis of <t>COX2</t> expression (× 400). D IF detection of cGMP–PKG pathway proteins (× 400). E Pearson’s R and Manders’ tM1 colocalization analysis. F Quantification of mean FI for pathway proteins. G qRT-PCR analysis of mRNA expression of pathway components. (mean ± SD, n = 3). ns, not significant; ▲▲ P < 0.01 vs. control group; * P < 0.05, ** P < 0.01 vs. OGD group; && P < 0.01 vs. Baicalin group; ## P < 0.01 vs. Kaempferide group; ★★ P < 0.01 vs. Baicalin + Kaempferide group
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    Regulation of the cGMP–PKG pathway by representative active components of ONSMP in OGD-induced H9C2 cells. A Determination of optimal concentrations of Baicalin and Kaempferide by CCK-8 assay. B Effects of Baicalin and Kaempferide on OGD-induced H9C2 cell viability. C IHC analysis of <t>COX2</t> expression (× 400). D IF detection of cGMP–PKG pathway proteins (× 400). E Pearson’s R and Manders’ tM1 colocalization analysis. F Quantification of mean FI for pathway proteins. G qRT-PCR analysis of mRNA expression of pathway components. (mean ± SD, n = 3). ns, not significant; ▲▲ P < 0.01 vs. control group; * P < 0.05, ** P < 0.01 vs. OGD group; && P < 0.01 vs. Baicalin group; ## P < 0.01 vs. Kaempferide group; ★★ P < 0.01 vs. Baicalin + Kaempferide group
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    Image Search Results


    Regulation of the cGMP–PKG pathway by representative active components of ONSMP in OGD-induced H9C2 cells. A Determination of optimal concentrations of Baicalin and Kaempferide by CCK-8 assay. B Effects of Baicalin and Kaempferide on OGD-induced H9C2 cell viability. C IHC analysis of COX2 expression (× 400). D IF detection of cGMP–PKG pathway proteins (× 400). E Pearson’s R and Manders’ tM1 colocalization analysis. F Quantification of mean FI for pathway proteins. G qRT-PCR analysis of mRNA expression of pathway components. (mean ± SD, n = 3). ns, not significant; ▲▲ P < 0.01 vs. control group; * P < 0.05, ** P < 0.01 vs. OGD group; && P < 0.01 vs. Baicalin group; ## P < 0.01 vs. Kaempferide group; ★★ P < 0.01 vs. Baicalin + Kaempferide group

    Journal: Chinese Medicine

    Article Title: Optimized New Shengmai Powder suppresses ferroptosis in ischemic cardiomyocytes via cGMP-PKG signalling

    doi: 10.1186/s13020-026-01364-6

    Figure Lengend Snippet: Regulation of the cGMP–PKG pathway by representative active components of ONSMP in OGD-induced H9C2 cells. A Determination of optimal concentrations of Baicalin and Kaempferide by CCK-8 assay. B Effects of Baicalin and Kaempferide on OGD-induced H9C2 cell viability. C IHC analysis of COX2 expression (× 400). D IF detection of cGMP–PKG pathway proteins (× 400). E Pearson’s R and Manders’ tM1 colocalization analysis. F Quantification of mean FI for pathway proteins. G qRT-PCR analysis of mRNA expression of pathway components. (mean ± SD, n = 3). ns, not significant; ▲▲ P < 0.01 vs. control group; * P < 0.05, ** P < 0.01 vs. OGD group; && P < 0.01 vs. Baicalin group; ## P < 0.01 vs. Kaempferide group; ★★ P < 0.01 vs. Baicalin + Kaempferide group

    Article Snippet: H9C2 cells (CL-0089, Pronsei Life Science Co., Ltd., Wuhan, Hubei, China) were routinely cultured in high-glucose DMEM supplemented with 10% FBS and 1% penicillin–streptomycin at 37 °C in a humidified CO2 incubator (Heracell VIOS 160i, Thermo Scientific, MA, USA) under 5% CO 2 .

    Techniques: CCK-8 Assay, Expressing, Quantitative RT-PCR, Control