beta 2-Microglobulin (B2M) forms the light chain of Class I MHC molecules. It has been measured in a variety of body fluids, including serum/plasma, saliva, CSF, and urine. B2M freely passes through the glomerular membrane, but it is nearly completely reabsorbed and degraded in proximal tubule cells. Clinically, serum B2M is elevated in rheumatoid arthritis, systemic lupus erythematosus, viral infections, and conditions associated with decreased glomerular filtration.
Human beta 2-Microglobulin Quantikine IVD ELISA Kit
R&D Systems | Catalog # DBM200
Key Product Details
Assay Length
Sample Type & Volume Required Per Well
Sensitivity
Assay Range
Product Summary for Human beta 2-Microglobulin Quantikine IVD ELISA Kit
Product Specifications
Assay Type
Format
Measurement
Detection Method
Conjugate
Species
Specificity
Cross-reactivity
Interference
Precision
Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays) Samples of known concentration were tested in separate assays to assess inter-assay precision.
Serum
| Intra-Assay Precision | Inter-Assay Precision | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 | 4 | 5 | 6 |
| n | 10 | 10 | 10 | 40 | 40 | 40 | 40 | 40 | 40 |
| Mean (pg/mL) | 0.9 | 1.4 | 8.4 | 0.9 | 1.3 | 8.9 | 1.1 | 3.2 | 8.0 |
| Standard Deviation | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| CV% | 8.1 | 6.3 | 5.3 | 9.2 | 6.8 | 4.8 | 8.9 | 6.9 | 6.0 |
Urine
| Intra-Assay Precision | Inter-Assay Precision | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 | |||
| n | 10 | 10 | 10 | 40 | 40 | 40 | |||
| Mean (pg/mL) | 1.2 | 3.3 | 8.6 | 1.1 | 3.4 | 8.7 | |||
| Standard Deviation | 0 | 0 | 0 | 0 | 0 | 0 | |||
| CV% | 7.4 | 5.3 | 4.4 | 9.2 | 5.6 | 4.9 | |||
Recovery for Human beta 2-Microglobulin Quantikine IVD ELISA Kit
The recovery of human beta 2-Microglobulin spiked to levels throughout the range of the assay in various matrices was evaluated.
| Sample Type | Average % Recovery | Range % |
|---|---|---|
| Serum (n=0) | 98 | 86.7-113.3 |
| Urine (n=0) | 105 | 86.7-113.3 |
Linearity
Five samples were assayed at serial two-fold dilutions. The data below are typical of the assay.
Scientific Data Images for Human beta 2-Microglobulin Quantikine IVD ELISA Kit
Human beta 2-Microglobulin In Vitro Diagnostic Standard Curve
Preparation and Storage
Shipping
Stability & Storage
Background: beta 2-Microglobulin
Alternate Names
Gene Symbol
Additional beta 2-Microglobulin Products
Product Documents for Human beta 2-Microglobulin Quantikine IVD ELISA Kit
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Related Research Areas
Citations for Human beta 2-Microglobulin Quantikine IVD ELISA Kit
Customer Reviews for Human beta 2-Microglobulin Quantikine IVD ELISA Kit (2)
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Customer Images
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Sample Tested: UrineVerified Customer | Posted 11/07/2016
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Sample Tested: Human DialysateVerified Customer | Posted 08/15/2016I use the kit for twom times, each used half plate. The first one is excelent, standards and QC are all in the right range and low deviation. However for the second assay, the low QC is out of range and the highest standard is bout 35% bias.
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Protocols
View specific protocols for Human beta 2-Microglobulin Quantikine IVD ELISA Kit (DBM200):
- Prepare all reagents as directed in the product insert.
- Remove excess microplate strips from the plate frame, return them to the foil pouch containing the desiccant pack, and reseal.
- Add 20 µL of Standard, Control, or sample to the appropriate wells.
- Add 100 µL of Conjugate Solution to each well.
- Add 100 µL of Antibody Solution to each well. Cover with a plate sealer, and incubate at room temperature for 1 hour.
- Aspirate each well and wash, repeating the process 5 times for a total of 6 washes.
- Add 100 µL Substrate Solution to each well. Cover with a new plate sealer, and incubate at room temperature for 15 minutes.
- Add 100 µL of Stop Solution to each well. Read at 450 nm within 30 minutes. Set wavelength correction to 620 nm.





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