ELK3556-48T, Human TNNI2(Troponin I Type 2, Fast Skeletal) ELISA Kit, 48T

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ELK3556-96T, Human TNNI2(Troponin I Type 2, Fast Skeletal) ELISA Kit, 96T

2.963,10 RON

Human TNNI2(Troponin I Type 2, Fast Skeletal) ELISA Kit

SKU
ELK3556-96T

Alternative Names: AMCD2B; DA2B; FSSV; Troponin I Fast Twitch 2; Troponin I, fast-twitch isoform

Species: Human

Assay Type: Sandwich

Sensitivity: 30 pg/mL

Standard: 5000 pg/mL

Detection range: 78.13-5000 pg/mL

Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Cardiovascular biology;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human TNNI2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TNNI2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human TNNI2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human TNNI2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: AMCD2B; DA2B; FSSV; Troponin I Fast Twitch 2; Troponin I, fast-twitch isoform

Species: Human

Assay Type: Sandwich

Sensitivity: 30 pg/mL

Standard: 5000 pg/mL

Detection range: 78.13-5000 pg/mL

Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Cardiovascular biology;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human TNNI2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TNNI2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human TNNI2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human TNNI2 in the samples is then determined by comparing the OD of the samples to the standard curve.