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Horse IL-12 p40 DIY ELISA Kit

SKU:
KES0138
Product Type:
ELISA Kit
Reactivity:
Horse
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
Interleukin-12 subunit beta, IL-12B, Cytotoxic lymphocyte matuRation factor 40 kDa subunit, CLMF p40, IL-12 subunit p40, NK cell stimulatory factor chain 2, NKSF2
€1,259
Frequently bought together:

Description

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Horse IL-12 p40 DIY ELISA Kit

The Equine IL-12 p40 ELISA Kit is specifically designed for the precise measurement of interleukin-12 p40 levels in equine serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit provides accurate and reproducible results, making it an ideal tool for a variety of research applications.Interleukin-12 p40 is a key cytokine involved in regulating the immune response, particularly in Th1 cell differentiation and activation. Its dysregulation has been linked to various inflammatory and autoimmune diseases in horses, making it a valuable biomarker for studying these conditions and exploring potential therapeutic interventions.

Overall, the Equine IL-12 p40 ELISA Kit offers researchers a reliable and efficient method for investigating the role of interleukin-12 p40 in equine health and disease, advancing our understanding of equine immunology and potentially leading to new treatment strategies.

Product Name:Horse IL-12 p40 DIY ELISA
Product Code:KES0138
Species:Horse
Target:IL-12 p40
Synonyms:Interleukin-12 subunit beta, IL-12B, Cytotoxic lymphocyte matuRation factor 40 kDa subunit, CLMF p40, IL-12 subunit p40, NK cell stimulatory factor chain 2, NKSF2
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-Horse IL-12 p40 Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Horse IL-12 p40 Polyclonal Antibody Detection Antibody 50 µg
Horse IL-12 p40 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 Horse IL-12 p40 DIY ELISA kit from Assay Genie can assay for IL-12 p40 in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Horse IL-12 p40 DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for IL-12 p40 using our unique combination of capture and detection antibodies.

Each Horse IL-12 p40 DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an IL-12 p40 ELISA. IL-12 p40 antibodies in this kit have been determined to function in an ELISA with the IL-12 p40 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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