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Rabbit VEGF-A 121 DIY ELISA Kit (KES0169)

SKU:
KES0169
Product Type:
ELISA Kit
Reactivity:
Rabbit
Applications:
ELISA
ELISA Type:
DIY ELISA
Size:
10 Plates
Synonyms:
VEGFA, MVCD1, VEGF, VPF, L VEGFA, VEGF A
€1,259

Description

system_update_altDatasheet

Rabbit VEGF-A 121 DIY ELISA Kit

The Rabbit VEGF-A 121 ELISA Kit is specifically designed for the precise measurement of Vascular Endothelial Growth Factor A (VEGF-A) 121 levels in rabbit serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit delivers dependable and consistent results, making it an indispensable tool for various research applications.VEGF-A 121 is a key factor involved in angiogenesis, the process of forming new blood vessels from pre-existing ones. It plays a vital role in various physiological processes, including wound healing, embryonic development, and tumor growth.

By accurately measuring VEGF-A 121 levels, researchers can gain insights into the mechanisms underlying angiogenesis and potentially develop novel therapeutic strategies for diseases such as cancer, cardiovascular disorders, and retinopathies.Overall, the Rabbit VEGF-A 121 ELISA Kit provides researchers with a reliable and efficient method for studying VEGF-A 121 and its implications in different biological processes and disease states.

Product Name:Rabbit VEGF-A 121 DIY ELISA
Product Code:KES0169
Species:Rabbit
Target:VEGF-A
Synonyms:VEGFA, MVCD1, VEGF, VPF, L VEGFA, VEGF A
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-Rabbit VEGF-A 121 Polyclonal Antibody Capture Antibody 100 µg
Biotinylated Anti-Rabbit VEGF-A 121 Polyclonal Antibody Detection Antibody 50 µg
Rabbit VEGF-A 121 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 Rabbit VEGF-A 121 DIY ELISA kit from Assay Genie can assay for VEGF-A in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues. Rabbit VEGF-A 121 DIY ELISA Kit from Assay Genie allows researchers to develop their own ELISA plates for VEGF-A using our unique combination of capture and detection antibodies.

Each Rabbit VEGF-A 121 DIY ELISA Kit contains capture antibody, standard, and detection antibody for development of an VEGF-A ELISA. VEGF-A antibodies in this kit have been determined to function in an ELISA with the VEGF-A 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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