ELK4093-48T, Human PLD2(Phospholipase D2) ELISA Kit, 48T

ELK4093-48T, Human PLD2(Phospholipase D2) ELISA Kit, 48T

ELK4094-48T, Human PSAT1(Phosphoserine Aminotransferase 1) ELISA Kit, 48T

ELK4094-48T, Human PSAT1(Phosphoserine Aminotransferase 1) ELISA Kit, 48T

ELK4093-96T, Human PLD2(Phospholipase D2) ELISA Kit, 96T

3.012,90 RON

Human PLD2(Phospholipase D2) ELISA Kit

SKU
ELK4093-96T

Alternative Names: PLD1C; Choline Phosphatase 2; Phosphatidylcholine-hydrolyzing phospholipase D2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.55 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;

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 PLD2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PLD2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human PLD2, biotin-conjugated antibody and enzyme-conjugated Avidin 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 PLD2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PLD1C; Choline Phosphatase 2; Phosphatidylcholine-hydrolyzing phospholipase D2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.55 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;

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 PLD2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PLD2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human PLD2, biotin-conjugated antibody and enzyme-conjugated Avidin 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 PLD2 in the samples is then determined by comparing the OD of the samples to the standard curve.