ELK8678-96T, TMAO(Trimethylamine-N-oxide) ELISA Kit, 96T

ELK8678-96T, TMAO(Trimethylamine-N-oxide) ELISA Kit, 96T

ELK8679-96T, Horse cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 96T

ELK8679-96T, Horse cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 96T

ELK8679-48T, Horse cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 48T

2.439,50 RON

Horse cAMP(Cyclic Adenosine Monophosphate) ELISA Kit

SKU
ELK8679-48T

Alternative Names: c-AMP; 3'-5'-Cyclic Adenosine Monophosphate; Adenosine Cyclophosphate

Species: Horse

Assay Type: Competitive Inhibition

Sensitivity: 92.5 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

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

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;

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

Mai multe informatii
Price 2.050,00 RON (preturile sunt fara TVA)
Description

Alternative Names: c-AMP; 3'-5'-Cyclic Adenosine Monophosphate; Adenosine Cyclophosphate

Species: Horse

Assay Type: Competitive Inhibition

Sensitivity: 92.5 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

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

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;

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