Description
IL-13R/CD213alpha1 Colorimetric Cell-Based ELISA Kit
The IL-13R (CD213alpha1) Colorimetric Cell-Based ELISA Kit is a cutting-edge tool designed for the sensitive and accurate detection of IL-13 receptor levels in cell culture samples. This innovative kit offers high specificity and precision, guaranteeing consistent and trustworthy results for various research applications.IL-13R, also known as CD213alpha1, plays a critical role in the immune system by mediating the effects of interleukin-13 (IL-13), a key cytokine involved in inflammatory responses and allergic reactions.
Detection of IL-13R levels can provide valuable insights into the underlying mechanisms of autoimmune diseases, asthma, and other immune-related disorders.The IL-13R (CD213alpha1) Colorimetric Cell-Based ELISA Kit is a valuable resource for researchers studying immune responses, inflammation, and therapeutic targets related to IL-13 signaling pathways. With its user-friendly protocol and exceptional performance, this kit is a must-have for any laboratory conducting research in the field of immunology.
| Product Name: | IL-13R/CD213alpha1 Colorimetric Cell-Based ELISA Kit |
| Product Code: | CBCAB00711 |
| ELISA Type: | Cell-Based |
| Target: | IL-13R/CD213alpha1 |
| Reactivity: | Human, Mouse, Rat |
| Dynamic Range: | > 5000 Cells |
| Detection Method: | Colorimetric 450 nmStorage/Stability:4°C/6 Months |
| Format: | 96-Well Microplate |
The IL-13R/CD213alpha1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect IL-13R/CD213alpha1 protein expression profile in cells. The kit can be used for measuring the relative amounts of IL-13R/CD213alpha1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on IL-13R/CD213alpha1.
Qualitative determination of IL-13R/CD213alpha1 concentration is achieved by an indirect ELISA format. In essence, IL-13R/CD213alpha1 is captured by IL-13R/CD213alpha1-specific primary antibodies while the HRP-conjugated secondary antibodies bind the Fc region of the primary antibody. Through this binding, the HRP enzyme conjugated to the secondary antibody can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of the Cell-Based ELISA, multiple normalization methods are needed:
| 1. | A monoclonal antibody specific for human GAPDH is included to serve as an internal positive control in normalizing the target absorbance values. |
| 2. | Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method may be used to determine cell density. After staining, the results can be analysed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted. |
| Database Information: | Gene ID: 3597, UniProt ID: P78552, OMIM: 300119, Unigene: Hs.496646 |
| Gene Symbol: | IL13RA1 |
| Sub Type: | None |
| UniProt Protein Function: | IL13R: Binds with low affinity to interleukin-13 (IL13). Together with IL4RA can form a functional receptor for IL13. Also serves as an alternate accessory protein to the common cytokine receptor gamma chain for interleukin-4 (IL4) signaling, but cannot replace the function of IL2RG in allowing enhanced interleukin-2 (IL2) binding activity. Belongs to the type I cytokine receptor family. Type 5 subfamily. |
| UniProt Protein Details: | Protein type:Membrane protein, integral; Receptor, cytokine Chromosomal Location of Human Ortholog: Xq24 Cellular Component: interleukin-13 receptor complex; plasma membrane Molecular Function:hematopoietin/interferon-class (D200-domain) cytokine receptor activity; protein binding Biological Process: cell surface receptor linked signal transduction; cytokine and chemokine mediated signaling pathway |
| NCBI Summary: | The protein encoded by this gene is a subunit of the interleukin 13 receptor. This subunit forms a receptor complex with IL4 receptor alpha, a subunit shared by IL13 and IL4 receptors. This subunit serves as a primary IL13-binding subunit of the IL13 receptor, and may also be a component of IL4 receptors. This protein has been shown to bind tyrosine kinase TYK2, and thus may mediate the signaling processes that lead to the activation of JAK1, STAT3 and STAT6 induced by IL13 and IL4. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P78552 |
| NCBI GenInfo Identifier: | 2494718 |
| NCBI Gene ID: | 3597 |
| NCBI Accession: | P78552.1 |
| UniProt Secondary Accession: | P78552,O95646, Q5JSL4, Q99656, Q9UDY5, |
| UniProt Related Accession: | P78552 |
| Molecular Weight: | 31,659 Da |
| NCBI Full Name: | Interleukin-13 receptor subunit alpha-1 |
| NCBI Synonym Full Names: | interleukin 13 receptor subunit alpha 1 |
| NCBI Official Symbol: | IL13RA1Â Â |
| NCBI Official Synonym Symbols: | NR4; CT19; CD213A1; IL-13Ra  |
| NCBI Protein Information: | interleukin-13 receptor subunit alpha-1 |
| UniProt Protein Name: | Interleukin-13 receptor subunit alpha-1 |
| UniProt Synonym Protein Names: | Cancer/testis antigen 19; CT19; CD_antigen: CD213a1 |
| Protein Family: | Interleukin-13 receptor |
| UniProt Gene Name: | IL13RA1Â Â |
| UniProt Entry Name: | I13R1_HUMAN |
| Component | Quantity |
| 96-Well Cell Culture Clear-Bottom Microplate | 2 plates |
| 10X TBS | 24 mL |
| Quenching Buffer | 24 mL |
| Blocking Buffer | 50 mL |
| 15X Wash Buffer | 50 mL |
| Primary Antibody Diluent | 12 mL |
| 100x Anti-Phospho Target Antibody | 60 µL |
| 100x Anti-Target Antibody | 60 µL |
| Anti-GAPDH Antibody | 60 µL |
| HRP-Conjugated Anti-Rabbit IgG Antibody | 12 mL |
| HRP-Conjugated Anti-Mouse IgG Antibody | 12 mL |
| SDS Solution | 12 mL |
| Stop Solution | 24 mL |
| Ready-to-Use Substrate | 12 mL |
| Crystal Violet Solution | 12 mL |
| Adhesive Plate Seals | 2 seals |
The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:
- Microplate reader able to measure absorbance at 450 nm and/or 595 nm for Crystal Violet Cell Staining (Optional)
- Micropipettes with capability of measuring volumes ranging from 1 µL to 1 ml
- 37% formaldehyde (Sigma Cat# F-8775) or formaldehyde from other sources
- Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
- Graph paper or computer software capable of generating or displaying logarithmic functions
- Absorbent papers or vacuum aspirator
- Test tubes or microfuge tubes capable of storing ≥1 ml
- Poly-L-Lysine (Sigma Cat# P4832 for suspension cells)
- Orbital shaker (optional)
- Deionized or sterile water
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
| Step | Procedure |
| 1. | Seed 200 µL of 20,000 adherent cells in culture medium in each well of a 96-well plate. The plates included in the kit are sterile and treated for cell culture. For suspension cells and loosely attached cells, coat the plates with 100 µL of 10 µg/ml Poly-L-Lysine (not included) to each well of a 96-well plate for 30 minutes at 37°C prior to adding cells. |
| 2. | Incubate the cells for overnight at 37°C, 5% CO2. |
| 3. | Treat the cells as desired. |
| 4. | Remove the cell culture medium and rinse with 200 µL of 1x TBS, twice. |
| 5. | Fix the cells by incubating with 100 µL of Fixing Solution for 20 minutes at room temperature. The 4% formaldehyde is used for adherent cells and 8% formaldehyde is used for suspension cells and loosely attached cells. |
| 6. | Remove the Fixing Solution and wash the plate 3 times with 200 µL 1x Wash Buffer for five minutes each time with gentle shaking on the orbital shaker. The plate can be stored at 4°C for a week. |
| 7. | Add 100 µL of Quenching Buffer and incubate for 20 minutes at room temperature. |
| 8. | Wash the plate 3 times with 1x Wash Buffer for 5 minutes each time. |
| 9. | Add 200 µL of Blocking Buffer and incubate for 1 hour at room temperature. |
| 10. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 11. | Add 50 µL of 1x primary antibodies (Anti-IL-13R/CD213alpha1 Antibody and/or Anti-GAPDH Antibody) to the corresponding wells, cover with Parafilm and incubate for 16 hours (overnight) at 4°C. If the target expression is known to be high, incubate for 2 hours at room temperature. |
| 12. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 13. | Add 50 µL of 1x secondary antibodies (HRP-Conjugated AntiRabbit IgG Antibody or HRP-Conjugated Anti-Mouse IgG Antibody) to corresponding wells and incubate for 1.5 hours at room temperature. |
| 14. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 15. | Add 50 µL of Ready-to-Use Substrate to each well and incubate for 30 minutes at room temperature in the dark. |
| 16. | Add 50 µL of Stop Solution to each well and read OD at 450 nm immediately using the microplate reader. |
(Additional Crystal Violet staining may be performed if desired – details of this may be found in the kit technical manual.)
