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Bovine LIF DIY ELISA Kit

SKU:
KES0108
Product Type:
ELISA Kit
Reactivity:
Bovine
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
LIF, CDF, DIA, HILDA, MLPLI
€1,259
Frequently bought together:

Description

system_update_altDatasheet

Bovine LIF DIY ELISA Kit

The Bovine LIF (Leukemia Inhibitory Factor) ELISA Kit is specially designed for the precise measurement of LIF levels in bovine serum, plasma, and cell culture supernatants. With exceptional sensitivity and specificity, this kit delivers accurate and consistent results, making it an invaluable tool for a broad range of research applications.LIF is a critical cytokine that plays a crucial role in various biological processes, including embryonic development, immune response, and hematopoiesis.

It is also involved in maintaining pluripotency in stem cells and promoting cell differentiation. Dysregulation of LIF has been linked to several diseases, making it a key biomarker for studying these conditions and developing potential therapeutic interventions.Overall, the Bovine LIF ELISA Kit provides researchers with a reliable and efficient method for exploring the functions of LIF in bovine physiology and pathology, ultimately advancing our understanding of this important cytokine.

Product Name:Bovine LIF DIY ELISA
Product Code:KES0108
Species:Bovine
Target:LIF
Synonyms:LIF, CDF, DIA, HILDA, MLPLI
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 LIF Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Bovine LIF Polyclonal Antibody Detection Antibody 50 µg
Bovine LIF 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 LIF DIY ELISA kit from Assay Genie can assay for LIF in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Bovine LIF DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for LIF using our unique combination of capture and detection antibodies.

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