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mt-cox1 antibody  (ABclonal Biotechnology)


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    Structured Review

    ABclonal Biotechnology mt-cox1 antibody
    Mt Cox1 Antibody, supplied by ABclonal Biotechnology, 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/mt-cox1+antibody/cox+2+antibody/pm39447668-129-75-76
    Average 90 stars, based on 1 article reviews
    mt-cox1 antibody - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: Decreased Mrpl42 expression exacerbates myocardial ischemia and reperfusion injury by inhibiting mitochondrial translation.
    Article Snippet: Primary antibodies against the following proteins were used: β-actin (ABclonal Technology Co., Ltd., China, AC004), HSP90 (Cell Signaling Technology, #4874S), Mrpl42 (ABclonal Technology Co., Ltd., China, A12811), cleavedcaspase 3 (Cell Signaling Technology, #9664), MT-ND1 (ABclonal Technology Co., Ltd., China, A18316), MT-ND2 (ABclonal Technology Co., Ltd., China, A17968), MT-ND3 (ABclonal Technology Co., Ltd., China, A17969), MT-ND4 (ABclonal Technology Co., Ltd., China, A9941), MT-ND5 (ABclonal Technology Co., Ltd., China, A17972), MTND6 (ABclonal Technology Co., Ltd., China, A17991), MT-COX1 (ABclonal Technology Co., Ltd., China, A17889), MT-COX2 (ABclonal Technology Co., Ltd., China, A17965), MT-COX3 (ABclonal Technology Co., Ltd., China, A17891), MT-ATP6 (ABclonal Technology Co., Ltd., China, A17960), MT-ATP8 (ABclonal Technology Co., Ltd., China, A17890), VDAC1 (ABclonal Technology Co., Ltd., China, A19707), Nrf2 (ABclonal Technology Co., Ltd., China, A1244), puromycin (ABclonal Technology Co., Ltd., China, A21205), Drp1 (ABclonal Technology Co., Ltd., China, A21968), Mfn1 (ABclonal Technology Co., Ltd., China, A21293), Mfn2 (ABclonal Technology Co., Ltd., China, A19678), Opa1 (ABclonal Technology Co., Ltd., China, A9833), p-Drp1 (S616) (Cell Signaling Technology, Inc. #3455) and p-Drp1 (S637) (Abcam Limited.



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    Mt Cox1 Antibody, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Mitochondrial network show signs of disorganization in striatal (upper panels) and cortical (lower panels) regions of NAGLU −/− mice Forty μm-thick coronal brain sections of 8-month-old wild type (WT) and NAGLU −/− mice were stained with the mitochondrial marker mitochondrially encoded cytochrome c oxidase I <t>(MT-CO1,</t> cytochrome c oxidase subunit 1 COX1). Nuclei were stained with Hoechst.
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    Image Search Results


    Effect of supplementation with 10-formyl-THF or formate on cisplatin-resistant cell survival and apoptotic cell death in cells with DLAT knockdown. Cells cultured under sublethal doses of cisplatin were treated with 10-formyl-THF ( a ) or formate ( b ) at indicated concentrations for 48 h. Apoptosis (top) and cell viability (bottom) were determined. 10-formyl-THF rescues cisplatin-resistant cell growth ( c ) and MT-CO2 expression ( d ) in cells lacking K44 MTHFD2 acetylation. Cisplatin-treated cells expressing K44R MTHFD2 were subjected to 10 μM 10-formyl-THF for 24 h followed by annexin V staining, cell viability assay, and assessment of MT-CO1, MT-CO2, and COXIV levels by immunoblotting and quantitative RT-PCR. Cells expressing the acetyl-mimetic mutant form of MTHFD2 K44Q were included for comparison. Effect of MT-CO2 overexpression on cisplatin-resistant cell growth in cells lacking K44 MTHFD2 acetylation ( e ) or DLAT ( f ) by K44R MTHFD2 expression or DLAT knockdown, respectively. Data are mean ± SD from 4 independent biological replicates for ( d ) and 3 for ( a – c , e , f ). P values were determined by one-way ANOVA. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Non-canonical dihydrolipoyl transacetylase promotes chemotherapy resistance via mitochondrial tetrahydrofolate signaling

    doi: 10.1038/s41467-025-63892-3

    Figure Lengend Snippet: Effect of supplementation with 10-formyl-THF or formate on cisplatin-resistant cell survival and apoptotic cell death in cells with DLAT knockdown. Cells cultured under sublethal doses of cisplatin were treated with 10-formyl-THF ( a ) or formate ( b ) at indicated concentrations for 48 h. Apoptosis (top) and cell viability (bottom) were determined. 10-formyl-THF rescues cisplatin-resistant cell growth ( c ) and MT-CO2 expression ( d ) in cells lacking K44 MTHFD2 acetylation. Cisplatin-treated cells expressing K44R MTHFD2 were subjected to 10 μM 10-formyl-THF for 24 h followed by annexin V staining, cell viability assay, and assessment of MT-CO1, MT-CO2, and COXIV levels by immunoblotting and quantitative RT-PCR. Cells expressing the acetyl-mimetic mutant form of MTHFD2 K44Q were included for comparison. Effect of MT-CO2 overexpression on cisplatin-resistant cell growth in cells lacking K44 MTHFD2 acetylation ( e ) or DLAT ( f ) by K44R MTHFD2 expression or DLAT knockdown, respectively. Data are mean ± SD from 4 independent biological replicates for ( d ) and 3 for ( a – c , e , f ). P values were determined by one-way ANOVA. Source data are provided as a Source Data file.

    Article Snippet: Antibodies against MTHFD2 (41377/D8W9U), myc-Tag (2278/71D10), phospho-Histone gamma H2AX S139 (9718/20E3), phospho-53BP1 S1778 (2675), COX1/MT-CO1 (62101), COX2/MT-CO2 (31219), COX IV (4850/3E11), acetyl-lysine (9441), Bcl-xL (2762), Bcl2 (15071), Mcl-1 (39224/D5V5L), Bad (9268/11E3), Bim (2933/C34C5), PARP (9542), Histone H3 (4499/D1H2), LC3A/B-I/II (4108), and p62 (5114) were purchased from Cell Signaling Technology.

    Techniques: Knockdown, Cell Culture, Expressing, Staining, Viability Assay, Western Blot, Quantitative RT-PCR, Mutagenesis, Comparison, Over Expression

    Mitochondrial network show signs of disorganization in striatal (upper panels) and cortical (lower panels) regions of NAGLU −/− mice Forty μm-thick coronal brain sections of 8-month-old wild type (WT) and NAGLU −/− mice were stained with the mitochondrial marker mitochondrially encoded cytochrome c oxidase I (MT-CO1, cytochrome c oxidase subunit 1 COX1). Nuclei were stained with Hoechst.

    Journal: iScience

    Article Title: Metabolic rewiring and autophagy inhibition correct lysosomal storage disease in mucopolysaccharidosis IIIB

    doi: 10.1016/j.isci.2024.108959

    Figure Lengend Snippet: Mitochondrial network show signs of disorganization in striatal (upper panels) and cortical (lower panels) regions of NAGLU −/− mice Forty μm-thick coronal brain sections of 8-month-old wild type (WT) and NAGLU −/− mice were stained with the mitochondrial marker mitochondrially encoded cytochrome c oxidase I (MT-CO1, cytochrome c oxidase subunit 1 COX1). Nuclei were stained with Hoechst.

    Article Snippet: rabbit anti-COX1/MT-CO1 antibody , Cell Signaling Technology , Cat# 62101.

    Techniques: Staining, Marker

    Journal: iScience

    Article Title: Metabolic rewiring and autophagy inhibition correct lysosomal storage disease in mucopolysaccharidosis IIIB

    doi: 10.1016/j.isci.2024.108959

    Figure Lengend Snippet:

    Article Snippet: rabbit anti-COX1/MT-CO1 antibody , Cell Signaling Technology , Cat# 62101.

    Techniques: Recombinant, Modification, Protease Inhibitor, Expressing, Clone Assay, Control, Generated, Knock-Out, Software