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Bovine CCL4 (MIP-1 beta) DIY ELISA Kit

SKU:
KES0002
Product Type:
ELISA Kit
Reactivity:
Bovine
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
CCL4, ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Bovine CCL4 (MIP-1 beta)DIY ELISA Kit

The Bovine CCL4/MIP-1 Beta ELISA Kit is a powerful tool for accurately measuring levels of CCL4/MIP-1 Beta in bovine serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring dependable and consistent results for a variety of research purposes.CCL4/MIP-1 Beta is a key chemokine involved in immune responses, inflammation, and cell migration. It plays a critical role in various physiological and pathological processes, including infectious diseases, autoimmune disorders, and inflammatory conditions.

By accurately measuring CCL4/MIP-1 Beta levels, researchers can gain valuable insights into these processes and potentially identify new therapeutic targets.Overall, the Bovine CCL4/MIP-1 Beta ELISA Kit is a valuable tool for researchers studying the immune system, inflammatory diseases, and host-pathogen interactions in bovine models. Its high sensitivity and accuracy make it an essential component of any research toolkit.

Product Name:Bovine CCL4 (MIP-1 beta) DIY ELISA
Product Code:KES0002
Species:Bovine
Target:CCL4
Synonyms:CCL4, ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4
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-Bovine CCL4 (MIP-1 beta) Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Bovine CCL4 (MIP-1 beta) Polyclonal Antibody Detection Antibody 50 µg
Bovine CCL4 (MIP-1 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 Bovine CCL4 (MIP-1 beta) DIY ELISA kit from Assay Genie can assay for CCL4 in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Bovine CCL4 (MIP-1 beta) DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for CCL4 using our unique combination of capture and detection antibodies.

Each Bovine CCL4 (MIP-1 beta) DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an CCL4 ELISA. CCL4 antibodies in this kit have been determined to function in an ELISA with the CCL4 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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