Rabbit PD-L1 DIY ELISA Kit
- SKU:
- KES0162
- Product Type:
- ELISA Kit
- Reactivity:
- Rabbit
- Applications:
- ELISA
- ELISA Type:
- DIY ELISA
- Size:
- 10 Plates
- Synonyms:
- B7-H, B7H1, PDL1, PD-L1, PDCD1L1, PDCD1LG1, CD274
Description
Rabbit PD-L1 DIY ELISA Kit
The Rabbit PD-L1 (Programmed Death Ligand 1) ELISA Kit is a powerful tool for the precise measurement of PD-L1 levels in rabbit samples, including serum, plasma, and cell culture supernatants. With its exceptional sensitivity and specificity, this kit ensures accurate and consistent results, making it ideal for various research purposes.PD-L1 is a key immune checkpoint protein that plays a critical role in regulating immune responses and maintaining immune tolerance. Dysregulation of PD-L1 expression is implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases.
As a result, studying PD-L1 levels can provide valuable insights into disease pathogenesis and potential therapeutic targets.The Rabbit PD-L1 ELISA Kit from Assay Genie offers researchers a reliable and efficient solution for quantifying PD-L1 levels in rabbit samples, enabling in-depth investigations into the role of PD-L1 in different physiological and pathological processes. Trust in this kit to deliver accurate and reproducible data for advancing your research endeavors.
| Product Name: | Rabbit PD-L1 DIY ELISA |
| Product Code: | KES0162 |
| Species: | Rabbit |
| Target: | PD-L1 |
| Synonyms: | B7-H, B7H1, PDL1, PD-L1, PDCD1L1, PDCD1LG1, CD274 |
| Application: | ELISA |
| ELISA Type: | DIY ELISA Kit |
| Size: | 10 Plates |
| Shipping: | Room temperature |
| Storage: | Stable for up to twelve months from date of receipt at 2-8°C. |
| Description | Usage | Quantity |
| Anti-Rabbit PD-L1 Polyclonal Antibody | Capture Antibody | 100 µg |
| Biotinylated Anti-Rabbit PD-L1 Polyclonal Antibody | Detection Antibody | 50 µg |
| Rabbit PD-L1 Recombinant Protein | Standard | 5 µg |
| Reagent | Suggested Formulation |
| DPBS: | 0.008M sodium phosphate, 0.002M potassium phosphate, 0.14M sodium chloride, 0.01M potassium chloride, pH 7.4 |
| 96-well ELISA Plate: | Clear, flat-bottom, high-binding 96-well plate, 8-wells per strip, 350 µL per well (ELISA Plates: KESAP003) |
| Standard and Sample Diluent: | The optimal Standard and Sample Diluent will need to be determined for each sample type to obtain optimal recovery and linearity. The appropriate Standard and Sample Diluent will mimic the sample's response to a known quantity of protein standard and will provide linear results when diluted. Often a 1:4 dilution of the sample in Reagent Diluent will provide acceptable recovery and linearity. |
| Reagent Diluent and Blocking Buffer: | 4% BSA in DPBS, 0.2 µm filtered |
| Wash Buffer: | 0.05% Tween®-20 in DPBS |
| Streptavidin-HRP: | Enzymatic reagent to react with biotinylated detection antibody (Streptavidin-HRP: KESAP002) |
| Substrate: | 3,3',5,5'-tetramethylbenzidine (TMB) Substrate (ELISA Accessory Pack: KESAP001) |
| Stop Solution: | 0.18 M Sulfuric Acid (ELISA Accessory Pack: KESAP001) |
| Plate Sealer: | Adhesive film to prevent evaporation |
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
| Step | Procedure |
| 1. | Prepare Capture Antibody in DPBS at desired working concentration. |
| 2. | Add 100 µL of Capture Antibody Working Solution to appropriate wells. |
| 3. | Cover plate with Plate Sealer and incubate at room temperature (20-25°C) for 12-24 hours. |
| 4. | Empty Capture Antibody Working Solution from plate. Blot plate onto paper towels or other absorbent material. |
| 5. | Add 100 µL of Blocking Buffer to appropriate wells. |
| 6. | Cover plate with Plate Sealer and incubate at room temperature for 1-3 hours. |
| 7. | Empty Blocking Buffer from plate. Blot plate onto paper towels or other absorbent material. |
| 8. | Prepare Standard and sample as desired with Standard and Sample Diluent. |
| 9. | Add 100 µL of Standard or sample to appropriate wells. Note: Run each Standard or sample in duplicate. |
| 10. | Cover plate with Plate Sealer and incubate at room temperature for 1 hour. |
| 11. | Wash plate FOUR times with Wash Buffer. Note: Gently squeeze the long sides of plate frame before washing to ensure all strips remain securely in the frame. Empty plate contents. Use a squirt wash bottle to vigorously fill each well completely with 1X Wash Buffer, then empty plate contents. Repeat procedure three additional times for a total of FOUR washes. Blot plate onto paper towels or other absorbent material. |
| 12. | Prepare Detection Antibody in Reagent Diluent at desired working concentration. |
| 13. | Add 100 µL of Detection Antibody Working Solution to each well. |
| 14. | Cover plate with Plate Sealer and incubate at room temperature for 1 hour. |
| 15. | Wash plate FOUR times with Wash Buffer as described in step 11. |
| 16. | Prepare Streptavidin-HRP in Reagent Diluent at desired working concentration. |
| 17. | Add 100 µL of Streptavidin-HRP Working Solution to each well. |
| 18. | Cover plate with Plate Sealer and incubate at room temperature for 30 minutes. |
| 19. | Wash plate FOUR times with Wash Buffer as described in step 11. |
| 20. | Add 100 µL of TMB Substrate Solution to each well. |
| 21. | Develop the plate in the dark at room temperature for 30 minutes or as desired. Note: Do NOT cover plate with Plate Sealer. |
| 22. | Stop reaction by adding 100 µL of Stop Solution to each well. |
| 23. | Measure absorbance on a plate reader at 450 nm. |
The Rabbit PD-L1 DIY ELISA kit from Assay Genie can assay for PD-L1 in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Rabbit PD-L1 DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for PD-L1 using our unique combination of capture and detection antibodies.
Each Rabbit PD-L1 DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an PD-L1 ELISA. PD-L1 antibodies in this kit have been determined to function in an ELISA with the PD-L1 standard provided. Optimal buffers, concentrations, incubation times, incubation temperatures, and methods for the ELISA have not been determined and require optimisation for the development of this kit. A working knowledge of ELISA is strongly recommended.
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