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Human a1M(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit
ELK2013
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48 T $320.00
96 T $458.00
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Overview

Product name: Human a1M(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit
Reactivity: Human
Alternative Names: AMBP; UTI; HCP; EDC1; HI30; IATIL; ITILC; ITI; ITIL; Alpha 1 Microglobulin/Bikunin Precursor; Growth-inhibiting protein 19; Uristatin; Uronic-Acid-Rich Protein; Trypstatin
Assay Type: Sandwich
Sensitivity: 6.1 pg/mL
Standard: 800 pg/mL
Detection Range: 12.5-800 pg/mL
Sample Type: Serum, plasma, urine and other biological fluids
Assay Length: 3.5h
Research Area: Infection immunity;Immune molecule;Kidney biomarker;
Uniprot ID: P02760
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 a1M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human a1M. 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 a1M, 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 a1M in the samples is then determined by comparing the OD of the samples to the standard curve.

Standard curve

Concentration (pg/mL) OD Corrected OD
800.00 1.941 1.852
400.00 1.562 1.473
200.00 1.087 0.998
100.00 0.735 0.646
50.00 0.593 0.504
25.00 0.312 0.223
12.50 0.206 0.117
0.00 0.089 0.000

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 a1M and the recovery rates were calculated by comparing the measured value to the expected amount of a1M in samples.
Matrix Recovery range Average
serum(n=5) 82-95% 88%
EDTA plasma(n=5) 80-94% 87%
Heparin plasma(n=5) 89-101% 95%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of a1M and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Matrix 1:2 1:4 1:8 1:16
serum(n=5) 87-98% 92-105% 83-92% 89-98%
EDTA plasma(n=5) 79-92% 88-96% 77-91% 85-93%
Heparin plasma(n=5) 88-97% 91-103% 86-92% 89-97%