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Porcine TNF alpha DIY ELISA Kit

SKU:
KES0071
Product Type:
ELISA Kit
Reactivity:
Porcine
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
TNF, DIF, TNF-alpha, TNFA, TNFSF2, TNLG1F, TNF alpha
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Porcine TNF alpha DIY ELISA Kit

The Swine TNF-alpha ELISA Kit from Assay Genie is specifically designed for the accurate detection of TNF-alpha levels in swine serum, plasma, and cell culture supernatants. With high sensitivity and specificity, this kit ensures reliable and reproducible results, making it an ideal tool for a wide range of research applications.TNF-alpha, or Tumor Necrosis Factor alpha, is a key cytokine involved in inflammatory responses and immune regulation. It plays a crucial role in various physiological and pathological processes, including infection, autoimmune diseases, and cancer.

Monitoring TNF-alpha levels is essential for understanding and studying these conditions, as well as for developing potential therapies. With the Swine TNF-alpha ELISA Kit, researchers can accurately measure TNF-alpha levels in swine samples, providing valuable insights into the role of this important cytokine in various biological processes. This kit is easy to use, with clear instructions and reliable performance, making it a valuable tool for any laboratory conducting research on swine immune responses and inflammatory pathways.

Product Name:Porcine TNF alpha DIY ELISA
Product Code:KES0071
Species:Porcine
Target:TNF alpha
Synonyms:TNF, DIF, TNF-alpha, TNFA, TNFSF2, TNLG1F, TNF alpha
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 TNF alpha Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Porcine TNF alpha Polyclonal Antibody Detection Antibody 50 µg
Porcine TNF alpha 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 TNF alpha DIY ELISA kit from Assay Genie can assay for TNF alpha in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Porcine TNF alpha DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for TNF alpha using our unique combination of capture and detection antibodies.

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