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ELK8712-96T, Human ASRGL1(L-asparaginase) ELISA Kit, 96T

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ELK8712-48T, Human ASRGL1(L-asparaginase) ELISA Kit, 48T

2.142,00 RON

Human ASRGL1(L-asparaginase) ELISA Kit

SKU
ELK8712-48T

Alternative Names: ASRGL1; L-asparaginase; L-asparagine amidohydrolase; Isoaspartyl dipeptidase; Asparaginase-like protein 1; ALP; CRASH

Species: Human

Assay Type: Sandwich

Sensitivity: 0.3 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Cancer

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 ASRGL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ASRGL1. 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 ASRGL1, 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 ASRGL1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ASRGL1; L-asparaginase; L-asparagine amidohydrolase; Isoaspartyl dipeptidase; Asparaginase-like protein 1; ALP; CRASH

Species: Human

Assay Type: Sandwich

Sensitivity: 0.3 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Cancer

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 ASRGL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ASRGL1. 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 ASRGL1, 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 ASRGL1 in the samples is then determined by comparing the OD of the samples to the standard curve.