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Rat MIP-3b ELISA Kit
Origin of place China
Model 96T
Supplier Shanghai Transhold Tech. Dev. Co.,Ltd.
Price 480USD
Hits 627
Updated 7/7/2012
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This Rat MIP-3b ELISA kit is to be used for the in vitro quantitative determination of MIP-3b concentrations in serum, plasma, cell culture supernatant, tissue fluid.and other biological fluids. This kit is intended for LABORATORY RESEARCH USE ONLY and is not for use in diagnostic or therapeutic procedures.

This Rat MIP-3b ELISA kit is a ready-to-use 4-hour solid phase immunoassay capable of measuring MIP-3b levels in serum, plasma, cell culture supernatant, tissue fluid and other biological fluids in the range of 0 to 2000 pg/mL. This assay has shown no cross-reactivity with various other cytokines super-family proteins, and is expected to be used effectively for further investigations into the relationship between Rat MIP-3b and various diseases.

Summary protocol:
1. Add 100µl of each Standards and samples into appropriate wells.
2. Gently mix for 30 seconds. Cover well and incubate at 37°C for 130 minutes.
3. Wash the microwell strips 5X.
4. Add 100µl of 1×Biotin into each well at the same rate and in the same order as the specimens were added. Gently mix for 30 seconds. Cover well and incubate at 37°C for 60 minutes.
5. Wash the plate by following the procedure in step 3.
6. Add 100µl of 1x HRP into each well at the same rate and in the same order as the Biotin was added. Gently mix for 30 seconds. Cover well and incubate at 37°C for 30 minutes.
7. Wash the plate by following the procedure in step 3.
8. Add 100µl of TMB Substrate into each well at the same rate and in the same order as the HRP was added. Gently mix for 10 seconds. Cover well and incubate at 37°C for 15±10 minutes. Protect from light.
9. Add 100µl of Stop Solution into each well at the same rate and in the same order as the TMB substrate solution was added. Gently mix for 30 seconds.
10. Set the microplate reader wavelength at 450nm and measure the optical density (OD) of each well. The plate should be read within 30 minutes after addition of the stop solution.

TYPICAL DATA

Results of a typical standard run of a Rat MIP-3b ELISA are shown below. Any variation in standard diluent, operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in result. The following examples are for the purpose of illustration only, and should not be used to calculate unknowns. Each user should obtain their own standard curve.


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