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Porcine IFN beta DIY ELISA Kit

SKU:
KES0110
Product Type:
ELISA Kit
Reactivity:
Porcine
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
IFNB1, IFB, IFF, IFN-beta, IFNB
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Porcine IFN beta DIY ELISA Kit

The Swine IFN-Beta ELISA Kit (KES0110) is specifically designed for the accurate measurement of interferon-beta levels in swine samples such as serum, plasma, and cell culture supernatants. This kit offers high sensitivity and specificity, ensuring precise and reproducible results for a variety of research applications.Interferon-beta is a key cytokine involved in the immune response, particularly in the defense against viral infections. It plays a crucial role in regulating the immune system and has been implicated in various diseases such as autoimmune disorders and viral infections.

As such, monitoring interferon-beta levels can provide valuable insights into the immune response and aid in the development of potential therapeutic interventions.Overall, the Swine IFN-Beta ELISA Kit (KES0110) is a valuable tool for researchers studying the immune system in swine models and investigating the role of interferon-beta in various disease processes. With its high sensitivity and reliability, this kit is an essential component for advancing research in immunology and virology.

Product Name:Porcine IFN beta DIY ELISA
Product Code:KES0110
Species:Porcine
Target:IFN beta
Synonyms:IFNB1, IFB, IFF, IFN-beta, IFNB
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-Porcine IFN beta Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Porcine IFN beta Polyclonal Antibody Detection Antibody 50 µg
Porcine IFN beta 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 Porcine IFN beta DIY ELISA kit from Assay Genie can assay for IFN beta in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Porcine IFN beta DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for IFN beta using our unique combination of capture and detection antibodies.

Each Porcine IFN beta DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an IFN beta ELISA. IFN beta antibodies in this kit have been determined to function in an ELISA with the IFN beta 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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