Human ABCG1 (ATP Binding Cassette Transporter G1) CLIA Kit (HUES00370)
- SKU:
- HUES00370
- Product Type:
- ELISA Kit
- ELISA Type:
- CLIA Kit
- Size:
- 96 Assays
- Sensitivity:
- 18.75pg/mL
- Range:
- 31.25-2000pg/mL
- ELISA Type:
- Sandwich
- Reactivity:
- Human
- Sample Type:
- Serum, plasma and other biological fluids
- Research Area:
- Cell Biology
Description
Product Name: | Human ABCG1 (ATP Binding Cassette Transporter G1) CLIA Kit |
SKU: | HUES00370 |
Target: | Human ABCG1 (ATP Binding Cassette Transporter G1) |
Size: | 96T |
Assay type: | Sandwich |
Assay time: | 4.5h |
Sensitivity: | 18.75 pg/mL |
Detection range: | 31.25-2000 pg/mL |
Kit component: |
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This CLIA kit uses the Sandwich-CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Human ABCG1. Standards or samples are added to the micro CLIA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human ABCG1 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human ABCG1, biotinylated detection antibody and Avidin-HRP conjugate will appear fluorescence. The Relative light unit (RLU) value is measured by the Chemiluminescence immunoassay analyzer. The RLU value is positively associated with the concentration of Human ABCG1. You can calculate the concentration of Human ABCG1 in the samples by comparing the RLU value of the samples to the standard curve.
Linearity: |
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Recovery: |
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Precision: |
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Sample type &Sample volume: | Serum, plasma and other biological fluids; 100μL |
Reproducibility: | Both intra-CV and inter-CV are < 15%. |
Application: | This CLIA kit applies to the in vitro quantitative determination of Human ABCG1 concentrations in Serum, plasma and other biological fluids. |
Specificity: | This kit recognizes Human ABCG1 in samples. No significant cross-reactivity or interference between Human ABCG1 and analogues was observed. |