Uteroglobin is small, secreted protein of the secretoglobin (SCGBs) family. Uteroglobin is expressed by Clara cells, the non-ciliated, non-mucous secretory cells predominant in lung bronchioles, and by other epithelia that communicate with the external environment. Uteroglob in binds to phospholipids and to several cell types, inhibiting inflammation, migration and invasion. It has been reported to bind the lipocalin-1 receptor.
Human Uteroglobin Quantikine ELISA Kit
R&D Systems | Catalog # DUGB00
Key Product Details
Assay Length
Sample Type & Volume Required Per Well
Sensitivity
Assay Range
Product Summary for Human Uteroglobin Quantikine ELISA Kit
Product Specifications
Assay Type
Format
Measurement
Detection Method
Conjugate
Species
Specificity
Cross-reactivity
Interference
精度
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) Three samples of known concentration were tested in separate assays to assess inter-assay precision.
Cell Culture Supernates, EDTA Plasma, Heparin Plasma, Serum
| Intra-Assay Precision | Inter-Assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) | 5.2 | 15.8 | 31.7 | 5.0 | 14.7 | 28.8 |
| Standard Deviation | 0.21 | 0.49 | 1.16 | 0.28 | 0.92 | 2.09 |
| CV% | 4.0 | 3.1 | 3.7 | 5.6 | 6.3 | 7.3 |
Human Milk, Saliva, Urine
| Intra-Assay Precision | Inter-Assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) | 5.1 | 15.4 | 31.3 | 5.2 | 15.4 | 29.9 |
| Standard Deviation | 0.29 | 0.34 | 1.04 | 0.31 | 0.72 | 2.25 |
| CV% | 5.7 | 2.2 | 3.3 | 6.0 | 4.7 | 7.5 |
Recovery for Human Uteroglobin Quantikine ELISA Kit
The recovery of Uteroglobin spiked to levels throughout the range of the assay in various matrices was evaluated.
| Sample Type | Average % Recovery | Range % |
|---|---|---|
| Cell Culture Media (n=4) | 102 | 99-109 |
| EDTA Plasma (n=4) | 95 | 85-107 |
| Heparin Plasma (n=4) | 95 | 86-109 |
| Serum (n=4) | 95 | 85-104 |
Linearity
To assess the linearity of the assay, samples containing and/or spiked with high concentrations of Uteroglobin were serially diluted with the appropriate Calibrator Diluent to produce samples with values within the dynamic range of the assay.
Scientific Data Images for Human Uteroglobin Quantikine ELISA Kit
Human Uteroglobin/SCGB1A1 ELISA Saliva/Urine/Human Milk Standard Curve
Human Uteroglobin/SCGB1A1 ELISA Cellculture Supernate/Serum/Plasma Standard Curve
Preparation and Storage
Shipping
Stability & Storage
Background: Uteroglobin/SCGB1A1
Alternate Names
Gene Symbol
Additional Uteroglobin/SCGB1A1 Products
Product Documents for Human Uteroglobin Quantikine ELISA Kit
Product Specific Notices for Human Uteroglobin Quantikine ELISA Kit
For research use only
⚠ WARNING: This product can expose you to chemicals including N,N-Dimethylforamide, which is known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.Related Research Areas
Citations for Human Uteroglobin Quantikine ELISA Kit
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Protocols
View specific protocols for Human Uteroglobin Quantikine ELISA Kit (DUGB00):
- Prepare all reagents, standard dilutions, and samples 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 100 µL of Assay Diluent to each well.
- Add 50 µL of Standard, control, or sample to each well. Cover with a plate sealer, and incubate at room temperature for 2 hours.
- Aspirate each well and wash, repeating the process 3 times for a total of 4 washes.
- Add 200 µL of Conjugate to each well. Cover with a new plate sealer, and incubate at room temperature for 2 hours.
- Aspirate and wash 4 times.
- Add 200 µL Substrate Solution to each well. Incubate at room temperature for 30 minutes. PROTECT FROM LIGHT.
- Add 50 µL of Stop Solution to each well. Read at 450 nm within 30 minutes. Set wavelength correction to 540 nm or 570 nm.





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