Lablisa® Human C3c(Complement C3 Convertase) ELISA Kit

Product Information

Lablisa® Human C3c(Complement C3 Convertase) ELISA Kit

Catalog No : LAB1112| 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 Human C3c. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human C3c. 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 C3c, 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 C3c in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:Human C3c(Complement C3 Convertase) ELISA Kit
Reactivity:Human
Alternative Names:C4b2a
Assay Type:Sandwich
Sensitivity:0.31 ng/mL
Standard:50 ng/mL
Detection Range:0.79-50 ng/mL
Sample Type:serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:3.5h
Research Area:Signal transduction;Infection immunity;Immune molecule;


Standard curve


Concentration (ng/mL)ODCorrected OD
50.001.7291.649
25.001.5651.485
12.500.9570.877
6.250.6520.572
3.130.3920.312
1.570.2860.206
0.790.2050.125
0.000.0800.000


Precision

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.


Recovery

Matrices listed below were spiked with certain level of recombinant C3c and the recovery rates were calculated by comparing the measured value to the expected amount of C3c in samples.

MatrixRecovery rangeAverage
serum(n=5)80-93%86%
EDTA plasma(n=5)95-107%101%
Heparin plasma(n=5)80-95%87%


Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of C3c and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Matrix1:21:41:81:16
serum(n=5)85-99%98-106%86-99%78-95%
EDTA plasma(n=5)89-97%85-94%87-96%85-97%
Heparin plasma(n=5)85-94%87-96%92-101%82-98%


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