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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using <t>RT-qPCR.</t> (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).
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| Validation of selected differentially expressed genes using RT-qPCR. (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).

Journal: Poultry Science

Article Title: Transcriptomic insights into thermal manipulation and heat stress in skeletal muscles of broiler chickens

doi: 10.1016/j.psj.2026.106846

Figure Lengend Snippet: | Validation of selected differentially expressed genes using RT-qPCR. (A) Relative expression levels of COL1A1, HSP90AA1, HSPH1, FKBP5, MSMB, LECT2, and SFRP4, measured by RT-qPCR across all experimental groups. Fold changes were calculated using ΔCt values, then expressed relative to the thermal neutral control (Con-N, 2^−ΔΔCt). Data are presented as mean and SEM (standard error of the mean) in error bars ( p-value < 0.001 = ***, p-value < 0.01 = **, p-value < 0.05 = *).

Article Snippet: Briefly, cDNA was synthesized from 2 μg of total RNA using SuperScript IV VILO Master Mix (Invitrogen, Thermo Fisher Scientific, DE, USA) and diluted 1:400. qPCR was performed in duplicate using BlasTaqTM 2X qPCR MasterMix (Applied Biological Materials Inc., BC, Canada) on a Rotor-Gene Q MDx 5plex system (Qiagen, Germany) in 20 μL reactions containing 10.0 μL MasterMix, 0.5 μL of each primer (10 μM), 2.0 μL diluted cDNA, and nuclease-free water.

Techniques: Biomarker Discovery, Quantitative RT-PCR, Expressing, Control