ELK7887-96T, LTB4(Leukotriene B4) ELISA Kit, 96T

ELK7887-96T, LTB4(Leukotriene B4) ELISA Kit, 96T

ELK7888-96T, ACH(Acetylcholine) ELISA Kit, 96T

ELK7888-96T, ACH(Acetylcholine) ELISA Kit, 96T

ELK7888-48T, ACH(Acetylcholine) ELISA Kit, 48T

1.814,75 RON

ACH(Acetylcholine) ELISA Kit

SKU
ELK7888-48T

Alternative Names: Acetylcholine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 5.31 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Infection immunity;Neuro science;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with ACH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to ACH. 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 ACH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Acetylcholine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 5.31 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Infection immunity;Neuro science;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with ACH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to ACH. 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 ACH in the samples is then determined by comparing the OD of the samples to the standard curve.