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ctni calibrator  (HyTest)


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    Structured Review

    HyTest ctni calibrator
    Figure 1. Simplified biosensor principle: The <t>cTnI–antibody–peroxidase</t> conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.
    Ctni Calibrator, supplied by HyTest, used in various techniques. Bioz Stars score: 96/100, based on 119 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ctni calibrator/product/HyTest
    Average 96 stars, based on 119 article reviews
    ctni calibrator - by Bioz Stars, 2026-04
    96/100 stars

    Images

    1) Product Images from "Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI)."

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    Journal: Biosensors

    doi: 10.3390/bios13040455

    Figure 1. Simplified biosensor principle: The cTnI–antibody–peroxidase conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.
    Figure Legend Snippet: Figure 1. Simplified biosensor principle: The cTnI–antibody–peroxidase conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.

    Techniques Used: Produced, Concentration Assay

    Figure 4. Microfluidic setup for the detection of cardiac troponin I (cTnI). The sample injection was performed by a 6-way valve and a continuous flow of running buffer and chemiluminescence substrate. After passing the peptide–BSA affinity column, the sample and substrate were combined 1:1 inside a mixer chip. This was followed by an incubation loop for preincubation and the flow cell for optical detection.
    Figure Legend Snippet: Figure 4. Microfluidic setup for the detection of cardiac troponin I (cTnI). The sample injection was performed by a 6-way valve and a continuous flow of running buffer and chemiluminescence substrate. After passing the peptide–BSA affinity column, the sample and substrate were combined 1:1 inside a mixer chip. This was followed by an incubation loop for preincubation and the flow cell for optical detection.

    Techniques Used: Injection, Incubation

    Figure 6. Quantification of cTnI expressed in E. coli using commercially available cTnI (Hytest 8RTI7) was used to calibrate the sandwich ELISA, as recommended by the supplier [31].
    Figure Legend Snippet: Figure 6. Quantification of cTnI expressed in E. coli using commercially available cTnI (Hytest 8RTI7) was used to calibrate the sandwich ELISA, as recommended by the supplier [31].

    Techniques Used: Sandwich ELISA

    Figure 9. Measurement series of cTnI in a concentration range between 0 and 64 µg/L and estimation of the dynamic range (see Figure S13).
    Figure Legend Snippet: Figure 9. Measurement series of cTnI in a concentration range between 0 and 64 µg/L and estimation of the dynamic range (see Figure S13).

    Techniques Used: Concentration Assay

    Figure 12. Measurement of human plasma, diluted 1:40 in running buffer and spiked with rec. cTnI in a range between 0 and 20 µg/L. The dilution factor is not included in the given concentrations.
    Figure Legend Snippet: Figure 12. Measurement of human plasma, diluted 1:40 in running buffer and spiked with rec. cTnI in a range between 0 and 20 µg/L. The dilution factor is not included in the given concentrations.

    Techniques Used: Clinical Proteomics

    Figure 13. Linearity of the cTnI detection in spiked human serum and plasma. Limits of detection (LoD) of 70 and 60 µg/L for serum and plasma, respectively, have been calculated.
    Figure Legend Snippet: Figure 13. Linearity of the cTnI detection in spiked human serum and plasma. Limits of detection (LoD) of 70 and 60 µg/L for serum and plasma, respectively, have been calculated.

    Techniques Used: Clinical Proteomics



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    Figure 1. Simplified biosensor principle: The <t>cTnI–antibody–peroxidase</t> conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.
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    Fig.2. Dose–response curves for the D-dimer and <t>cTnI</t> immunoassays. The error bars represent the standard deviation measured from three replicate microtitration wells. (A) The D-dimer assay exploiting 8D3F(ab0)2 as the solid-phase and FDP14 as the detection antibody. (j) 0 lg/ml free FDP14/8D3F(ab0)2, (d) 5 lg/ml free 8D3F(ab0)2, (.) 15 lg/ ml free 8D3F(ab0)2, (}) 5 lg/ml free FDP14, and (s) 15 lg/ml free FDP14. (B) The D-dimer assay exploiting FDP14 as the solid-phase and 8D3F(ab0)2 as the detection antibody. (j) 0 lg/ml free DP14/8D3F(ab0)2, (N) 5 lg/ml free 8D3F(ab0)2, (d) 15 lg/ml free 8D3F(ab0)2, (h) 1 lg/ml free FDP14, and (}) 5 lg/ml free FDP14. (C) The cTnI assay exploiting 8I7 as the solid-phase and 9707 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 9707, (.) 10 lg/ml free 9707, (d) 25 lg/ml free 9707, and (}) 10 lg/ml free 8I7. (D) The cTnI assay exploiting 9707 as the solid-phase and 8I7 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 8I7, (.) 10 lg/ml free 8I7, (d) 25 lg/ml free 8I7, and (}) 10 lg/ml free 9707.
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    Image Search Results


    Figure 1. Simplified biosensor principle: The cTnI–antibody–peroxidase conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 1. Simplified biosensor principle: The cTnI–antibody–peroxidase conjugate binds to the analyte cTnI (PDB 4Y99) and cannot interact with the peptide-functionalized column (coated with a peptide–BSA conjugate). The intensity of the chemiluminescence produced by the enzyme–substrate reaction is largely proportional to the analyte concentration in the sample.

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Produced, Concentration Assay

    Figure 4. Microfluidic setup for the detection of cardiac troponin I (cTnI). The sample injection was performed by a 6-way valve and a continuous flow of running buffer and chemiluminescence substrate. After passing the peptide–BSA affinity column, the sample and substrate were combined 1:1 inside a mixer chip. This was followed by an incubation loop for preincubation and the flow cell for optical detection.

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 4. Microfluidic setup for the detection of cardiac troponin I (cTnI). The sample injection was performed by a 6-way valve and a continuous flow of running buffer and chemiluminescence substrate. After passing the peptide–BSA affinity column, the sample and substrate were combined 1:1 inside a mixer chip. This was followed by an incubation loop for preincubation and the flow cell for optical detection.

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Injection, Incubation

    Figure 6. Quantification of cTnI expressed in E. coli using commercially available cTnI (Hytest 8RTI7) was used to calibrate the sandwich ELISA, as recommended by the supplier [31].

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 6. Quantification of cTnI expressed in E. coli using commercially available cTnI (Hytest 8RTI7) was used to calibrate the sandwich ELISA, as recommended by the supplier [31].

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Sandwich ELISA

    Figure 9. Measurement series of cTnI in a concentration range between 0 and 64 µg/L and estimation of the dynamic range (see Figure S13).

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 9. Measurement series of cTnI in a concentration range between 0 and 64 µg/L and estimation of the dynamic range (see Figure S13).

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Concentration Assay

    Figure 12. Measurement of human plasma, diluted 1:40 in running buffer and spiked with rec. cTnI in a range between 0 and 20 µg/L. The dilution factor is not included in the given concentrations.

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 12. Measurement of human plasma, diluted 1:40 in running buffer and spiked with rec. cTnI in a range between 0 and 20 µg/L. The dilution factor is not included in the given concentrations.

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Clinical Proteomics

    Figure 13. Linearity of the cTnI detection in spiked human serum and plasma. Limits of detection (LoD) of 70 and 60 µg/L for serum and plasma, respectively, have been calculated.

    Journal: Biosensors

    Article Title: Chemiluminescence Biosensor for the Determination of Cardiac Troponin I (cTnI).

    doi: 10.3390/bios13040455

    Figure Lengend Snippet: Figure 13. Linearity of the cTnI detection in spiked human serum and plasma. Limits of detection (LoD) of 70 and 60 µg/L for serum and plasma, respectively, have been calculated.

    Article Snippet: After another wash with PBST, 100 μL of the cTnI calibrator (recombinant cTnI from HyTest Ltd.) and the expressed cTnI (both diluted in LowCross-Buffer, Candor Bioscience GmbH) were pipetted and incubated for 1 h at room temperature.

    Techniques: Clinical Proteomics

    Fig.2. Dose–response curves for the D-dimer and cTnI immunoassays. The error bars represent the standard deviation measured from three replicate microtitration wells. (A) The D-dimer assay exploiting 8D3F(ab0)2 as the solid-phase and FDP14 as the detection antibody. (j) 0 lg/ml free FDP14/8D3F(ab0)2, (d) 5 lg/ml free 8D3F(ab0)2, (.) 15 lg/ ml free 8D3F(ab0)2, (}) 5 lg/ml free FDP14, and (s) 15 lg/ml free FDP14. (B) The D-dimer assay exploiting FDP14 as the solid-phase and 8D3F(ab0)2 as the detection antibody. (j) 0 lg/ml free DP14/8D3F(ab0)2, (N) 5 lg/ml free 8D3F(ab0)2, (d) 15 lg/ml free 8D3F(ab0)2, (h) 1 lg/ml free FDP14, and (}) 5 lg/ml free FDP14. (C) The cTnI assay exploiting 8I7 as the solid-phase and 9707 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 9707, (.) 10 lg/ml free 9707, (d) 25 lg/ml free 9707, and (}) 10 lg/ml free 8I7. (D) The cTnI assay exploiting 9707 as the solid-phase and 8I7 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 8I7, (.) 10 lg/ml free 8I7, (d) 25 lg/ml free 8I7, and (}) 10 lg/ml free 9707.

    Journal: Analytical biochemistry

    Article Title: Extension of dynamic range of sensitive nanoparticle-based immunoassays.

    doi: 10.1016/j.ab.2013.10.034

    Figure Lengend Snippet: Fig.2. Dose–response curves for the D-dimer and cTnI immunoassays. The error bars represent the standard deviation measured from three replicate microtitration wells. (A) The D-dimer assay exploiting 8D3F(ab0)2 as the solid-phase and FDP14 as the detection antibody. (j) 0 lg/ml free FDP14/8D3F(ab0)2, (d) 5 lg/ml free 8D3F(ab0)2, (.) 15 lg/ ml free 8D3F(ab0)2, (}) 5 lg/ml free FDP14, and (s) 15 lg/ml free FDP14. (B) The D-dimer assay exploiting FDP14 as the solid-phase and 8D3F(ab0)2 as the detection antibody. (j) 0 lg/ml free DP14/8D3F(ab0)2, (N) 5 lg/ml free 8D3F(ab0)2, (d) 15 lg/ml free 8D3F(ab0)2, (h) 1 lg/ml free FDP14, and (}) 5 lg/ml free FDP14. (C) The cTnI assay exploiting 8I7 as the solid-phase and 9707 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 9707, (.) 10 lg/ml free 9707, (d) 25 lg/ml free 9707, and (}) 10 lg/ml free 8I7. (D) The cTnI assay exploiting 9707 as the solid-phase and 8I7 as the detection antibody. (h) 0 lg/ml free 8I7/9707, (N) 5 lg/ml free 8I7, (.) 10 lg/ml free 8I7, (d) 25 lg/ml free 8I7, and (}) 10 lg/ml free 9707.

    Article Snippet: Materials and methods D-dimer and cTnI calibrators and clinical samples The D-dimer calibration material was prepared from partially purified D-dimer from human fibrin digested with human plasmin (Biokit, Barcelona, Spain), and human cTnI (native, tissue-derived cTnI–cardiac troponin T–troponin C complex) was purchased from HyTest (Turku, Finland).

    Techniques: Standard Deviation, D-dimer Assay