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ELK0329-96T, Human ACLY(ATP-citRate Synthase) ELISA Kit, 96T
2.475,20 RON
Human ACLY(ATP-citRate Synthase) ELISA Kit
SKU
ELK0329-96T
Alternative Names: ACL; ACLY; ATP citrate (pro S ) lyase; ATP citrate lyase; ATP citrate synthase; ATPCL; Citrate cleavage enzyme; CLATP
Species: Human
Assay Type: Sandwich
Sensitivity: 0.51 IU/mL
Standard: 100 IU/mL
Detection range: 1.57-100 IU/mL
Sample type: Serum, plasma, tissue homogenates and other biological fluids.
Assay length: 3.5h
Research Area: Metabonomics
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 ACLY. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACLY. 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 ACLY, 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 ACLY in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 2.080,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: ACL; ACLY; ATP citrate (pro S ) lyase; ATP citrate lyase; ATP citrate synthase; ATPCL; Citrate cleavage enzyme; CLATP Species: Human Assay Type: Sandwich Sensitivity: 0.51 IU/mL Standard: 100 IU/mL Detection range: 1.57-100 IU/mL Sample type: Serum, plasma, tissue homogenates and other biological fluids. Assay length: 3.5h Research Area: Metabonomics 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 ACLY. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACLY. 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 ACLY, 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 ACLY in the samples is then determined by comparing the OD of the samples to the standard curve. |
