Human beta Amyloid 1-40 enzyme-linked immunoassay kit

CAT: EH0111 Datasheet
Specification 96 Test
Sensitivity 2.92 pg/ml (50 μl);8.40 pg/ml (10 μl)
Standard Curve Range 31.25~2000 pg/ml
Standard Curve Gradient 7 Points
Number of Incubations 2
Sample Volume 50 μl/10 μl
Type Fully Ready-to-Use
Operation Duration 120min
pg/ml O.D. Average Corrected
0.00 0.0446 0.0451 0.0449
31.25 0.0817 0.0770 0.0794 0.0345
62.50 0.1291 0.1349 0.1320 0.0871
125.00 0.2772 0.2812 0.2792 0.2343
250.00 0.5233 0.5129 0.5181 0.4732
500.00 1.0246 1.0388 1.0317 0.9868
1000.00 1.8213 1.8056 1.8135 1.7686
2000.00 3.3130 3.3240 3.3185 3.2736

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(pg/ml) 757.9 168.5 48.0 703.8 202.7 42.7
Standard Deviation 40.9 7.1 1.8 22.1 5.6 2.4
Coefficient of Variation(%) 5.4 4.2 3.7 3.1 2.8 5.6

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays) Three samples of known concentration were tested six times on one plate to assess intra-assay precision.

Spike Recovery

The spike recovery was evaluated by spiking 3 levels of human beta Amyloid 1-40 into health human serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 84% to 122% with an overall mean recovery of 105%.

Sample Values

Sample Matrix Sample Evaluated Range (pg/ml) Detectable (%) Mean of Detectable (pg/ml)
Serum 30 n.d.- 907.22 37.5 198.85

Serum/Plasma – Thirty samples from apparently healthy volunteers were evaluated for the presence of beta Amyloid 1-40 in this assay. No medical histories were available for the donors.

Background: beta Amyloid 1-40

β-Amyloid (1-40), Iowa mutation is a biologically active peptide. (Several mutations in the beta amyloid precursor gene lead to autosomal dominant Alzheimer's disease in many families. Iowa mutations (where Asp 23 is replaced by Asn) are associated with severe brain amyloid vascular disease (CAA). The affected individuals have a missense mutation at APP 694. The mutated beta-amyloid peptides accumulate faster and form toxic fibrils.)

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