| ALX-201-124-C010 | 10 µg | 330.00 USD | ![]() |
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| Alternative Name: | Pentraxin 3, TSG14, TNF stimulated gene-14 |
| Concentration: | 0.1mg/ml. |
| MW: | ~42kDa. Due to glycosylation, PTX3 may migrate between 40-45kDa. |
| Formulation: | Liquid. In PBS containing 2% BSA and 0.1% sodium azide. |
| Source/Host: | Produced in CHO cells. Human full-length PTX3. |
| Application: | ELISA and Western blot standard together with MAb to PTX3 (Prod. No. ALX-804-464 (capture antibody)) and PAb to PTX3-Biotin (Prod. No. ALX-210-365B (detection antibody)). For Western blot standard use 0.1-1µg PTX3 per lane using mini gel system. |
| Long Term Storage: | -20°C |
| Handling: | Avoid freeze/thaw cycles. |
| Protocol: | Sandwich ELISA for PTX3 - 96 well-ELISA plates (Nunc MaxiSorp 446612) were coated with 100µl of MAb to PTX3 (human) (MNB4) (Prod. No. ALX-804-464), 1μg/ml in 100µl coating buffer (15mM carbonate buffer pH 9.6) and incubated overnight at 4°C. - After incubation, the plates were washed three times with 300µl/well of washing buffer (PBS + 0.05% Tween 20), and then 300µl of 5% dry milk in washing buffer were added to block non-specific binding. - The plates were incubated for 2 hours at room temperature and then washed three times with washing buffer. - 50µl (in duplicate) recombinant human PTX3 standard (Prod. No. ALX-201-124) (75pg/ml to 2.4ng/ml ), cell supernatants or biological fluids diluted in PBS without Ca and Mg + 2% BSA were added and then incubated for 2 hours at 37°C. - The plates were washed five times with washing buffer, and then 100µl of PAb to PTX3 (human) (Biotin) (Prod. No. ALX-210-365B) 50ng/ml in washing buffer were added in each well. - The plates were incubated for 1 hour at 37°C and then washed five times with 300µl of washing buffer. - 100 µl/well streptavidin-horseradish peroxidase diluted 1:4’000 were added and the plates incubated for 1 hour at room temperature. - After incubation the plates were washed 5 times with washing buffer and 100µl of TMB substrate solution was added to each well. After incubation for 10 min. at room-temperature, 50μl of stop-solution (1M H2SO4) was added. Subsequently, absorbance was read within 30min at 450nm. Note: Do not use heparin plasma or serum samples with this assay. EDTA samples are recommended. The detection value in serum is generally less than in plasma samples. |
