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Porcine CD40 Ligand DIY ELISA Kit

SKU:
KES0134
Product Type:
ELISA Kit
Reactivity:
Porcine
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
CD154, CD40L, HIGM1, IGM, IMD3, T-BAM, TNFSF5, TRAP, gp39, hCD40L, CD40LG
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Porcine CD40 Ligand DIY ELISA Kit

The Swine CD40 Ligand ELISA Kit is specifically designed for the precise measurement of CD40 Ligand levels in swine serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, guaranteeing consistent and trustworthy results for a variety of research purposes. CD40 Ligand is a key protein involved in immune response regulation, playing a crucial role in the activation of immune cells and the coordination of inflammatory processes. Its dysregulation has been linked to various diseases, including autoimmune disorders and inflammatory conditions, making it a valuable biomarker for exploring disease mechanisms and potential therapeutic targets.

The Swine CD40 Ligand ELISA Kit is a valuable tool for researchers studying immunology, inflammation, and related fields, providing a reliable method for quantifying CD40 Ligand levels in swine samples. With its ease of use and accurate results, this kit is essential for advancing our understanding of immune system function and disease pathology in swine models.

Product Name:Porcine CD40 Ligand DIY ELISA
Product Code:KES0134
Species:Porcine
Target:CD40 Ligand
Synonyms:CD154, CD40L, HIGM1, IGM, IMD3, T-BAM, TNFSF5, TRAP, gp39, hCD40L, CD40LG
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 CD40 Ligand Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Porcine CD40 Ligand Polyclonal Antibody Detection Antibody 50 µg
Porcine CD40 Ligand 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 CD40 Ligand DIY ELISA kit from Assay Genie can assay for CD40 Ligand in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Porcine CD40 Ligand DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for CD40 Ligand using our unique combination of capture and detection antibodies.

Each Porcine CD40 Ligand DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an CD40 Ligand ELISA. CD40 Ligand antibodies in this kit have been determined to function in an ELISA with the CD40 Ligand 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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