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primary antibodies against cyt-c  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc primary antibodies against cyt-c
    Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, <t>Bcl-2,</t> and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.
    Primary Antibodies Against Cyt C, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 174 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against cyt-c/product/Cell Signaling Technology Inc
    Average 90 stars, based on 174 article reviews
    primary antibodies against cyt-c - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Honokiol Provides Cardioprotection from Myocardial Ischemia/Reperfusion Injury (MI/RI) by Inhibiting Mitochondrial Apoptosis via the PI3K/AKT Signaling Pathway"

    Article Title: Honokiol Provides Cardioprotection from Myocardial Ischemia/Reperfusion Injury (MI/RI) by Inhibiting Mitochondrial Apoptosis via the PI3K/AKT Signaling Pathway

    Journal: Cardiovascular Therapeutics

    doi: 10.1155/2022/1001692

    Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, Bcl-2, and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.
    Figure Legend Snippet: Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, Bcl-2, and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.

    Techniques Used: Western Blot



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    Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, <t>Bcl-2,</t> and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.
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    MAPKs, NAMPT, and SIRT1 changes according to the group. (A) C26-induced cancer cachexia was associated either ERK and JNK activation, then NR administration significantly inactivated these cachexia-associated MAPKs. (B) <t>NAMPT1</t> was significantly decreased in cancer cachexia group, suggesting incomplete conversion of NAD + in cancer cachexia, whereas NR administration maintained NAMPT1 expression. (C) SIRT1 was significantly increased in cancer cachexia group, but not in the NR-treated group, suggesting that NR administration did not affect SIRT1-mediated muscle atrophy.
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    Image Search Results


    Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, Bcl-2, and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.

    Journal: Cardiovascular Therapeutics

    Article Title: Honokiol Provides Cardioprotection from Myocardial Ischemia/Reperfusion Injury (MI/RI) by Inhibiting Mitochondrial Apoptosis via the PI3K/AKT Signaling Pathway

    doi: 10.1155/2022/1001692

    Figure Lengend Snippet: Western blot analysis of apoptosis-associated proteins. Western blotting was utilized to evaluate the protein levels of cleaved caspase-9, Cyt-C, Bcl-2, and Bax. GAPDH acted as the internal reference ( n = 6 for each cohort). Data are articulated as mean ± SEM. ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.

    Article Snippet: Primary antibodies against Bcl-2 (Cell Signaling Technology (CST), Danvers, MA, USA), Bax (CST), Cyt-C (CST), caspase-9 (Abcam, Cambridge, MA, USA), PI3K (CST), p-PI3K (CST), AKT (CST), and p-AKT (CST) were used for protein detection.

    Techniques: Western Blot

    MAPKs, NAMPT, and SIRT1 changes according to the group. (A) C26-induced cancer cachexia was associated either ERK and JNK activation, then NR administration significantly inactivated these cachexia-associated MAPKs. (B) NAMPT1 was significantly decreased in cancer cachexia group, suggesting incomplete conversion of NAD + in cancer cachexia, whereas NR administration maintained NAMPT1 expression. (C) SIRT1 was significantly increased in cancer cachexia group, but not in the NR-treated group, suggesting that NR administration did not affect SIRT1-mediated muscle atrophy.

    Journal: Frontiers in Pharmacology

    Article Title: Nicotinamide Riboside Vitamin B3 Mitigated C26 Adenocarcinoma–Induced Cancer Cachexia

    doi: 10.3389/fphar.2021.665493

    Figure Lengend Snippet: MAPKs, NAMPT, and SIRT1 changes according to the group. (A) C26-induced cancer cachexia was associated either ERK and JNK activation, then NR administration significantly inactivated these cachexia-associated MAPKs. (B) NAMPT1 was significantly decreased in cancer cachexia group, suggesting incomplete conversion of NAD + in cancer cachexia, whereas NR administration maintained NAMPT1 expression. (C) SIRT1 was significantly increased in cancer cachexia group, but not in the NR-treated group, suggesting that NR administration did not affect SIRT1-mediated muscle atrophy.

    Article Snippet: Primary antibodies for Western blotting against NAMPT1, SIRT1, Pax7, ubiquitin, p-p38, ATGL (adipose triglyceride lipase), PARP-1, caspase-8, Bax, and Cyt c were from Cell Signaling Technology (Danvers, MA, United States).

    Techniques: Activation Assay, Expressing