
ELISA Complement Activity Analysis
| Productname |
Ba MicroVue™ Quidel® |
|
Quantification of the Complement Ba fragment |
| Cat-No. |
A034 |
| Range |
0.05 – 2.1 ng/ml |
| Sensitivity |
LOD: 0.011 ng/ml; LLOQ: 0.033 ng/ml |
| Incubation time |
3 hours |
| Sample volume |
10 µl (dilute plasma 1:1000, serum 1:2000), 25 µl urine (dilute 1:15) |
| Sample type |
EDTA Plasma, serum, urine |
| Sample preparation |
Serum / Plasma:
The Ba fragment of Factor B is susceptible to proteolysis. For optimal plasma results, K2 EDTA should be used. Collect blood sample and centrifuge immediately at 2-8°C. Assay immediately, do not store longer than 2 hours at 2-8°C. For longer storage -70°C.
Urine:
Collect preservative-free first Morning void (FMV) or second morning void (SMV) before 10:00 am. Store sample refrigerated (2-8°C) for less than
1 day, or freeze the sample at -70°C for longer storage.
Maximum 5 freeze and thaw cycles. |
| Reference values |
| Sample |
n |
Mean |
Range (ng/ml) |
| EDTA Plasma |
35 |
658 |
226-2153 |
| Serum |
29 |
1642 |
436-3362 |
| Urine |
16 |
7.7 |
0.6-27.0 |
|
| Species |
Human, African green monkey, cynomolgus monkey, rhesus monkey,
canine |
| Specificity |
Monoclonal mouse-antibody, specifically to capture the Ba fragment. |
| Tests |
96 |
| Method |
ELISA |
| Product informations |
- Kit Instructions (pdf-File 673 kb) - MSDS (pdf-File 112 kb) - Datasheet (pdf-File 513 kb) - Information (pdf-File 1170 kb)
|
| Intended use |
By quantifying the amount of Ba, the extent of alternative pathway activation at the time of sample collection can be determined.
Activation of the alternative pathway has been associated with a variety of disease states including SLE, chronic glomerulonephritis, rheumatoid arthritis, sickle cell anemia and gram negative bacterial infections.
The activation of the alternative complement pathway can be triggered by a variety of substances including microbial polysaccharides or lipids, gram-negative bacterial lipopolysaccharides, surface determinants present on some viruses, parasites, virally infected mammalian cells, and cancer cells. In autoimmune
diseases, the alternative complement pathway may contribute directly to tissue damage. Alternative complement pathway activation may also be an indicator of hemo-incompatibility of biomaterials.
Application
- kidney diseases
chronic glomerulonephritis
lupus nephritis
- skin diseases
dermatitis herpetiformis
pemphigus vulgaris
- age-related macular degeneration
- fetal loss in at risk pregnancy
- rheumatoid arthritis
- sickle cell anemia
|
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