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anti ctni  (Proteintech)


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    Proteintech anti ctni
    Anti Ctni, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 66 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ctni+antibody/Cardiac+Troponin+I+Antibody/pm41765115-50-5-12
    Average 95 stars, based on 66 article reviews
    anti ctni - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Recombinant:

    Article Title: An Alternating Current Electroosmotic Flow‐Based Ultrasensitive Electrochemiluminescence Microfluidic System for Ultrafast Monitoring, Detection of Proteins/miRNAs in Unprocessed Samples
    Article Snippet: .. Rabbit polyclonal anti‐cTnI antibody, mouse monoclonal anti‐cTnI antibody were purchased from Proteintech (Shanghai, China). cTnI recombinant protein was obtained from Abcam company (USA). .. Tris(2,2‐bipyridyl) dichlororuthenium (II) hexahydrate (Ru(bpy) 3 Cl 2 ·6H 2 O), cyclohexane, 1‐hexanol, tetraethyl orthosilicate (TEOS), NaCl, trehalose, triton X‐100, polyvinylpyrrolidone (PVP), tween 20, tripropylamine (TPrA), ammonium hydroxide (NH 3 ·H 2 O), and ethanol were all from Aladdin Chemistry Co., Ltd. (Shanghai, China).

    other:

    Article Title: Coxsackievirus A2 Leads to Heart Injury in a Neonatal Mouse Model
    Article Snippet: The following primary antibodies were used in this study: anti-CTGF, TIMP-4, MMP9, CTNI (Proteintech Group, Inc., Wuhan, China); anti-MMP8, MMP3 (Abways Biotechnology Co., Ltd., Shanghai, China); anti-BNP (Cloud-Clone Technology Co., Ltd., Wuhan, China); anti-pp65, p65, pERK1/2 (Thr202/Tyr204), CD45, pIκBα, IκBα, pJNK, JNK2, ERK1/2, pp38, p38, AKT, pAKT (Thr308), anti-mouse IgG and anti-rabbit IgG (Cell Signaling Biotechnology, Inc., MA, USA); anti-CD11b (Abcam Biotechnology, Inc., Cambridge, UK); anti-CVA2 VP1 antibody (prepared in our own laboratory).



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    Data show the mean ± SD with each sample as dot plots for the protein abundance of <t>phospholamban</t> <t>(PLN,</t> B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I <t>(cTnI,</t> E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.
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    Data show the mean ± SD with each sample as dot plots for the protein abundance of <t>phospholamban</t> <t>(PLN,</t> B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I <t>(cTnI,</t> E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.
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    Image Search Results


    Data show the mean ± SD with each sample as dot plots for the protein abundance of phospholamban (PLN, B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I (cTnI, E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.

    Journal: bioRxiv

    Article Title: Developmental Hypoxia Increases Susceptibility to Cardiac Ventricular Arrhythmias in Adult Offspring

    doi: 10.64898/2026.01.22.701057

    Figure Lengend Snippet: Data show the mean ± SD with each sample as dot plots for the protein abundance of phospholamban (PLN, B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I (cTnI, E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.

    Article Snippet: Membranes were incubated with primary antibodies (PLN [1/5000 dilution] – MA3-922, InVitrogen; phospho-PLN-T17 [1/1000 dilution] – AP0910, ABclonal; cTnI [1/1000 dilution] – MCA1208, Bio-Rad; phospho-cTnI [1/1000 dilution] – MCA2780, Bio-Rad; Calsequestrin-1 [1/5000 dilution] – PA1-913, InVitrogen; SERCA2 [1/2000 dilution] – ab3625, Abcam; NCX1 [1/1000 dilution] – R3F1, Swant; LTCC [1/1000 dilution] – ab2864, Abcam; RYR2 [1/1000 dilution] – ab302716, Abcam; phospho-RYR2-S2808 [1/1000 dilution] – PA5-105712, InVitrogen) overnight at 4°C, before secondary antibody incubation (IRDye® 800CW Goat anti-mouse for PLN, cTnI, phospho-cTnI, NCX1 and LTCC, IRDye® 800CW goat anti-rabbit for phospho-PLN-T17, Calsequestrin-1, SERCA2, RYR2 and phosphor-RYR2-S2808, both 1/20 000 dilution) at room temperature for one hour.

    Techniques: Quantitative Proteomics, MANN-WHITNEY

    Data show the mean ± SD with each sample as dot plots for the protein abundance of phospholamban (PLN, B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I (cTnI, E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.

    Journal: bioRxiv

    Article Title: Developmental Hypoxia Increases Susceptibility to Cardiac Ventricular Arrhythmias in Adult Offspring

    doi: 10.64898/2026.01.22.701057

    Figure Lengend Snippet: Data show the mean ± SD with each sample as dot plots for the protein abundance of phospholamban (PLN, B), phospho-PLN-T17 (C), ratio of phospho-PLN-T17 to PLN (D), cardiac troponin I (cTnI, E), phospho-cTnI (F), ratio of phospho-cTnI to cTnI (G), calsequestrin-1 (H), SERCA2 (I), ratio of SERCA2 to PLN (J), sodium-calcium exchanger 1 (NCX1, K), L-type calcium channel (LTCC, L), ryanodine receptor 2 (RYR2, M), phospho-RYR2-S2808 (N), ratio of phospho-RYR2-S2808 to RYR2 (O) and Connexin43 (Cx43, P). Data was analysed using an unpaired Student’s T-Test for all proteins except PLN, cTnI, NCX and phospho-cTnI/cTnI ratio which used a Mann-Whitney test (data not normally distributed). P<0.05 was considered significant. Normoxia = closed circles, Hypoxia = open circles.

    Article Snippet: Membranes were incubated with primary antibodies (PLN [1/5000 dilution] – MA3-922, InVitrogen; phospho-PLN-T17 [1/1000 dilution] – AP0910, ABclonal; cTnI [1/1000 dilution] – MCA1208, Bio-Rad; phospho-cTnI [1/1000 dilution] – MCA2780, Bio-Rad; Calsequestrin-1 [1/5000 dilution] – PA1-913, InVitrogen; SERCA2 [1/2000 dilution] – ab3625, Abcam; NCX1 [1/1000 dilution] – R3F1, Swant; LTCC [1/1000 dilution] – ab2864, Abcam; RYR2 [1/1000 dilution] – ab302716, Abcam; phospho-RYR2-S2808 [1/1000 dilution] – PA5-105712, InVitrogen) overnight at 4°C, before secondary antibody incubation (IRDye® 800CW Goat anti-mouse for PLN, cTnI, phospho-cTnI, NCX1 and LTCC, IRDye® 800CW goat anti-rabbit for phospho-PLN-T17, Calsequestrin-1, SERCA2, RYR2 and phosphor-RYR2-S2808, both 1/20 000 dilution) at room temperature for one hour.

    Techniques: Quantitative Proteomics, MANN-WHITNEY