ELK012ES-96T, EasyStep Human CRP(C Reactive Protein) ELISA Kit, 96T

ELK012ES-96T, EasyStep Human CRP(C Reactive Protein) ELISA Kit, 96T

ELK013ES-96T, EasyStep Human PRL(Prolactin) ELISA Kit, 96T

ELK013ES-96T, EasyStep Human PRL(Prolactin) ELISA Kit, 96T

ELK013ES-48T, EasyStep Human PRL(Prolactin) ELISA Kit, 48T

2.142,00 RON

EasyStep Human PRL(Prolactin) ELISA Kit

SKU
ELK013ES-48T

Alternative Names: LTH; Luteotropic Hormone

Species: Human

Assay Type: Sandwich

Sensitivity: 248 pg/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Serum

Assay length: 1.5h

Research Area: Endocrinology; Reproductive science; Genetic science; Hormone metabolism

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 PRL, and the Human PRL standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human PRL. After TMB substrate solution is added, only those wells that contain Human PRL and HRP-conjugated antibody 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 PRL in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: LTH; Luteotropic Hormone

Species: Human

Assay Type: Sandwich

Sensitivity: 248 pg/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Serum

Assay length: 1.5h

Research Area: Endocrinology; Reproductive science; Genetic science; Hormone metabolism

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 PRL, and the Human PRL standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human PRL. After TMB substrate solution is added, only those wells that contain Human PRL and HRP-conjugated antibody 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 PRL in the samples is then determined by comparing the OD of the samples to the standard curve.