Lablisa® Mouse ACE(Angiotensin I Converting Enzyme) ELISA Kit

Product Information

Lablisa® Mouse ACE(Angiotensin I Converting Enzyme) ELISA Kit 

Catalog No : LAB1001| Pack Size : 48T , 96T

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 Angiotensin I Converting Enzyme(ACE). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Angiotensin I Converting Enzyme(ACE). 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 Angiotensin I Converting Enzyme(ACE), 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 Angiotensin I Converting Enzyme(ACE) in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:Lablisa® Mouse ACE(Angiotensin I Converting Enzyme) ELISA Kit
Alternative Names:CD143; ACE1; DCP1; ACEI; ACE-I; Kininase II; Angiotensin-Converting Enzyme; Peptidyl-Dipeptidase A; Dipeptidyl Carboxypeptidase 1; Angiotensin-converting enzyme, soluble form
Assay Type:Sandwich
Sensitivity:0.142 ng/mL
Standard:20 ng/mL
Range:0.32-20 ng/mL
Sample Type:serum, plasma, tissue homogenates, cell lysates, cerebrospinal fluid, cell culture supernates and other biological fluids
Assay Length:3.5h
Research Area:Enzyme & Kinase;Cardiovascular biology;

Standard curve

Concentration (ng/mL)ODCorrected OD


Intra-assay Precision (Precision within an assay):CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays):CV%<10%

Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.


Matrices listed below were spiked with certain level of recombinant ACE and the recovery rates were calculated by comparing the measured value to the expected amount of ACE in samples.

MatrixRecovery rangeAverage
EDTA plasma(n=5)95-107%101%
Heparin plasma(n=5)96-104%



The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ACE and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

EDTA plasma(n=5)89-101%79-92%82-93%83-97%
Heparin plasma(n=5)82-103%81-91%85-101%81-90%

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