ELK8963-48T, Horse LZM(Lysozyme) ELISA Kit, 48T

ELK8963-48T, Horse LZM(Lysozyme) ELISA Kit, 48T

ELK8964-48T, Human SNCb(Synuclein beta) ELISA Kit, 48T

ELK8964-48T, Human SNCb(Synuclein beta) ELISA Kit, 48T

ELK8963-96T, Horse LZM(Lysozyme) ELISA Kit, 96T

3.736,60 RON

Horse LZM(Lysozyme) ELISA Kit

SKU
ELK8963-96T

Alternative Names: LYZ; Renal Amyloidosis; N-Acetylmuramide Glycanhydrolase; Muramidase; 1,4-beta-N-acetylmuramidase C

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.131 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Infection immunity;

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

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Description

Alternative Names: LYZ; Renal Amyloidosis; N-Acetylmuramide Glycanhydrolase; Muramidase; 1,4-beta-N-acetylmuramidase C

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.131 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Infection immunity;

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