ELK1847-96T, Mouse HSPB1(Heat Shock 27kDa Protein 1) ELISA Kit, 96T

ELK1847-96T, Mouse HSPB1(Heat Shock 27kDa Protein 1) ELISA Kit, 96T

ELK1848-96T, Mouse NTXI(Cross Linked N-Telopeptide Of Type I Collagen) ELISA Kit, 96T

ELK1848-96T, Mouse NTXI(Cross Linked N-Telopeptide Of Type I Collagen) ELISA Kit, 96T

ELK1848-48T, Mouse NTXI(Cross Linked N-Telopeptide Of Type I Collagen) ELISA Kit, 48T

2.142,00 RON

Mouse NTXI(Cross Linked N-Telopeptide Of Type I Collagen) ELISA Kit

SKU
ELK1848-48T

Alternative Names: NTX-I; NTX1

Species: Mouse

Assay Type: Competitive Inhibition

Sensitivity: 0.93 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: serum, plasma, urine and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Bone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse NTXI protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse NTXI. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Mouse NTXI in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: NTX-I; NTX1

Species: Mouse

Assay Type: Competitive Inhibition

Sensitivity: 0.93 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: serum, plasma, urine and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Bone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse NTXI protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse NTXI. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Mouse NTXI in the samples is then determined by comparing the OD of the samples to the standard curve.