Mouse Cardiovascular ELISA Kits
Mouse IL-25 CLIA Kit (MOES00119)
- SKU:
- MOES00119
- Product Type:
- ELISA Kit
- ELISA Type:
- CLIA Kit
- Size:
- 96 Assays
- Sensitivity:
- 4.69pg/mL
- Range:
- 7.81-500pg/mL
- ELISA Type:
- Sandwich
- Synonyms:
- IL25, IL17E
- Reactivity:
- Mouse
- Sample Type:
- Serum, plasma and other biological fluids
- Research Area:
- Cardiovascular
Description
| Assay type: | Sandwich |
| Format: | 96T |
| Assay time: | 4.5h |
| Reactivity: | Mouse |
| Detection method: | Chemiluminescence |
| Detection range: | 7.81-500 pg/mL |
| Sensitivity: | 4.69 pg/mL |
| Sample volume: | 100µL |
| Sample type: | Serum, plasma and other biological fluids |
| Repeatability: | CV < 15% |
| Specificity: | This kit recognizes Mouse IL25 CLIA Kit in samples. No significant cross-reactivity or interference between Mouse IL25 CLIA Kit and analogues was observed. |
This kit uses Sandwich-CLIA as the method. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Mouse IL25. Standards or samples are added to the appropriate micro CLIA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse IL25 and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Mouse IL25, biotinylated detection antibody and Avidin-HRP conjugate will appear fluorescence. The Relative light unit (RLU) value is measured spectrophotometrically by the Chemiluminescence immunoassay analyzer. The RLU value is positively associated with the concentration of Mouse IL25. The concentration of Mouse IL25 in the samples can be calculated by comparing the RLU of the samples to the standard curve.
| UniProt Protein Function: | MYDGF: was previously thought to support proliferation of lymphoid cells and was considered an interleukin. However, this activity has not been reproducible and the function of this protein is currently unknown. [provided by RefSeq, Jul 2008] |
| UniProt Protein Details: | Protein type:Secreted, signal peptide; Secreted Cellular Component: extracellular space; extracellular region Biological Process: positive regulation of phosphoinositide 3-kinase cascade; positive regulation of protein kinase B signaling cascade; positive regulation of angiogenesis; positive regulation of MAPKKK cascade; positive regulation of endothelial cell proliferation; positive regulation of transcription from RNA polymerase II promoter; positive regulation of protein amino acid phosphorylation; negative regulation of apoptosis |
| NCBI Summary: | The protein encoded by this gene was previously thought to support proliferation of lymphoid cells and was identified in error as interleukin 25. This activity has not been reproducible, however, and the function of this protein is currently unknown. [provided by RefSeq, Jul 2008] |
| UniProt Code: | Q9CPT4 |
| NCBI GenInfo Identifier: | 61221740 |
| NCBI Gene ID: | 28106 |
| NCBI Accession: | Q9CPT4. 1 |
| UniProt Secondary Accession: | Q9CPT4,Q3UG74, A2RSI7, |
| UniProt Related Accession: | Q9CPT4 |
| Molecular Weight: | 17,982 Da |
| NCBI Full Name: | UPF0556 protein C19orf10 homolog |
| NCBI Synonym Full Names: | DNA segment, Chr 17, Wayne State University 104, expressed |
| NCBI Official Symbol: | D17Wsu104e |
| NCBI Official Synonym Symbols: | Il25; Ly6elg |
| NCBI Protein Information: | UPF0556 protein C19orf10 homolog |
| UniProt Protein Name: | UPF0556 protein C19orf10 homolog |
| UniProt Synonym Protein Names: | Interleukin-25; IL-25; Stromal cell-derived growth factor SF20 |
| UniProt Gene Name: | D17Wsu104e |
| UniProt Entry Name: | CS010_MOUSE |
As the RLU values of the standard curve may vary according to the conditions of the actual assay performance (e. g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.
| Concentration (pg/mL) | RLU | Average | Corrected |
| 500 | 51509 51565 | 51537 | 51508 |
| 250 | 19098 22898 | 20998 | 20969 |
| 125 | 9398 9394 | 9396 | 9367 |
| 62.5 | 4454 4570 | 4512 | 4483 |
| 31.25 | 2308 2290 | 2299 | 2270 |
| 15.63 | 1251 1249 | 1250 | 1221 |
| 7.81 | 715 765 | 740 | 711 |
| 0 | 28 30 | 29 | -- |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Mouse IL25 CLIA Kit were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Mouse IL25 CLIA Kit were tested on 3 different plates, 20 replicates in each plate.
| Intra-assay Precision | Inter-assay Precision | |||||
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (pg/mL) | 25.89 | 72.08 | 223.85 | 27.29 | 67.26 | 222.83 |
| Standard deviation | 2.57 | 7.29 | 17.26 | 2.87 | 4.96 | 25.54 |
| C V (%) | 9.93 | 10.11 | 7.71 | 10.52 | 7.37 | 11.46 |
Recovery
The recovery of Mouse IL25 CLIA Kit spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
| Sample Type | Range (%) | Average Recovery (%) |
| Serum (n=5) | 93-107 | 98 |
| EDTA plasma (n=5) | 92-105 | 98 |
| Cell culture media (n=5) | 100-112 | 106 |
Linearity
Samples were spiked with high concentrations of Mouse IL25 CLIA Kit and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
| Serum (n=5) | EDTA plasma (n=5) | Cell culture media (n=5) | ||
| 1:2 | Range (%) | 83-96 | 93-103 | 95-109 |
| Average (%) | 90 | 98 | 102 | |
| 1:4 | Range (%) | 98-110 | 93-105 | 85-95 |
| Average (%) | 104 | 99 | 90 | |
| 1:8 | Range (%) | 89-103 | 98-113 | 86-99 |
| Average (%) | 95 | 105 | 93 | |
| 1:16 | Range (%) | 99-114 | 97-108 | 94-109 |
| Average (%) | 107 | 102 | 100 |
An unopened kit can be stored at 4°C for 1 month. If the kit is not used within 1 month, store the items separately according to the following conditions once the kit is received.
| Item | Specifications | Storage |
| Micro CLIA Plate(Dismountable) | 8 wells ×12 strips | -20°C, 6 months |
| Reference Standard | 2 vials | |
| Concentrated Biotinylated Detection Ab (100×) | 1 vial, 120 µL | |
| Concentrated HRP Conjugate (100×) | 1 vial, 120 µL | -20°C(shading light), 6 months |
| Reference Standard & Sample Diluent | 1 vial, 20 mL | 4°C, 6 months |
| Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
| HRP Conjugate Diluent | 1 vial, 14 mL | |
| Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
| Substrate Reagent A | 1 vial, 5 mL | 4°C (shading light) |
| Substrate Reagent B | 1 vial, 5 mL | 4°C (shading light) |
| Plate Sealer | 5 pieces | |
| Product Description | 1 copy | |
| Certificate of Analysis | 1 copy |
- Set standard, test sample and control (zero) wells on the pre-coated plate and record theirpositions. It is recommended to measure each standard and sample in duplicate. Note: addall solutions to the bottom of the plate wells while avoiding contact with the well walls. Ensuresolutions do not foam when adding to the wells.
- Aliquot 100µl of standard solutions into the standard wells.
- Add 100µl of Sample / Standard dilution buffer into the control (zero) well.
- Add 100µl of properly diluted sample (serum, plasma, tissue homogenates and otherbiological fluids. ) into test sample wells.
- Cover the plate with the sealer provided in the kit and incubate for 90 min at 37°C.
- Aspirate the liquid from each well, do not wash. Immediately add 100µL of BiotinylatedDetection Ab working solution to each well. Cover the plate with a plate seal and gently mix. Incubate for 1 hour at 37°C.
- Aspirate or decant the solution from the plate and add 350µL of wash buffer to each welland incubate for 1-2 minutes at room temperature. Aspirate the solution from each well andclap the plate on absorbent filter paper to dry. Repeat this process 3 times. Note: a microplatewasher can be used in this step and other wash steps.
- Add 100µL of HRP Conjugate working solution to each well. Cover with a plate seal andincubate for 30 min at 37°C.
- Aspirate or decant the solution from each well. Repeat the wash process for five times asconducted in step 7.
- Add 100µL of Substrate mixture solution to each well. Cover with a new plate seal andincubate for no more than 5 min at 37°C. Protect the plate from light.
- Determine the RLU value of each well immediately.
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