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Horse CCL3 (MIP-1 alpha) DIY ELISA Kit

SKU:
KES0035
Product Type:
ELISA Kit
Reactivity:
Horse
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Horse CCL3 (MIP-1 alpha)DIY ELISA Kit

The Equine CCL3/MIP-1 Alpha ELISA Kit is specifically designed for the precise quantification of C-C motif chemokine 3 (CCL3), also known as Macrophage Inflammatory Protein 1 Alpha (MIP-1 Alpha), in equine serum, plasma, and cell culture supernatants. This kit offers high sensitivity and specificity, ensuring accurate and dependable results for a variety of research purposes.CCL3/MIP-1 Alpha is a key chemokine involved in the inflammatory response, playing a crucial role in recruiting immune cells to sites of infection or injury.

Dysregulation of CCL3/MIP-1 Alpha has been linked to various inflammatory conditions in horses, making it a valuable biomarker for studying equine health and developing potential treatments.Overall, the Equine CCL3/MIP-1 Alpha ELISA Kit is an essential tool for researchers looking to investigate the role of CCL3/MIP-1 Alpha in equine physiology and pathology, providing valuable insights into immune responses and inflammatory processes in horses.

Product Name:Horse CCL3 (MIP-1 alpha) DIY ELISA
Product Code:KES0035
Species:Horse
Target:CCL3
Synonyms:CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3
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 CCL3 (MIP-1 alpha) Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Horse CCL3 (MIP-1 alpha) Polyclonal Antibody Detection Antibody 50 µg
Horse CCL3 (MIP-1 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 Horse CCL3 (MIP-1 alpha) DIY ELISA kit from Assay Genie can assay for CCL3 in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Horse CCL3 (MIP-1 alpha) DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for CCL3 using our unique combination of capture and detection antibodies.

Each Horse CCL3 (MIP-1 alpha) DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an CCL3 ELISA. CCL3 antibodies in this kit have been determined to function in an ELISA with the CCL3 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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