ELK8115-96T, LPA(Lysophosphatidic Acid) ELISA Kit, 96T

ELK8115-96T, LPA(Lysophosphatidic Acid) ELISA Kit, 96T

ELK8116-96T, cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 96T

ELK8116-96T, cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 96T

ELK8116-48T, cAMP(Cyclic Adenosine Monophosphate) ELISA Kit, 48T

2.439,50 RON

cAMP(Cyclic Adenosine Monophosphate) ELISA Kit

SKU
ELK8116-48T

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

Species: General

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 cAMP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 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 cAMP in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

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

Species: General

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 cAMP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 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 cAMP in the samples is then determined by comparing the OD of the samples to the standard curve.