Universal ELISA Buffer Set is a comprehensive solution kit containing commonly used buffers and reagents for ELISA procedures, including sandwich ELISA. The set includes coating buffer, blocking buffer, wash buffer, universal dilution buffer, chromogenic substrate, and stop solution, meeting the standard solution requirements for routine ELISA. Users only need to provide the ELISA detection antibodies (and biotin detection reagents if using a biotin system), microplates, and sealing films (and standards if absolute quantification is required) to perform ELISA.
ELISA (Enzyme-Linked Immunosorbent Assay) is a highly sensitive immunological technique that combines the specific reaction between antigen and antibody with the efficient catalytic action of an enzyme on its substrate. It is widely used across many fields in biology and medical science. Common types of ELISA include the double antibody sandwich ELISA (Sandwich ELISA), competitive ELISA, direct ELISA, and indirect ELISA. The double antibody sandwich ELISA, often abbreviated as sandwich ELISA, is one of the most common ELISA formats and can be used to determine the concentration of target molecules, such as specific proteins, in a sample.
Instructions for Use
Refer to the specific ELISA kit instructions for detailed procedural steps. The following describes the general for each solution in this set; conditions can be optimized according to actual experimental needs.
1. Coating Buffer
Use directly without dilution or reconstitution.Dilute the capture antibody to an appropriate concentration using the Coating Buffer.Add 100 µL per well to a blank microplate.Incubate overnight at 4°C, or for 2 hours at 37°C.
2. Blocking Buffer
Use directly without dilution or reconstitution.After coating, wash the plate 3 times with Wash Buffer (1X, preparation see step 3).Add 200 µL of Blocking Buffer per well and incubate at room temperature for 120 minutes.Discard the liquid, blot the plate dry, and proceed directly to subsequent steps such as primary antibody incubation.For preparing pre-coated plates: After room temperature blocking for 2 hours, discard the liquid and blot dry. Invert and dry the plate at 37°C for 90 minutes. Pre-coated plates can be sealed in a moisture-proof bag with desiccant or stored in other suitable conditions. Typically, they can be stored at 4°C for approximately six months.
3. Wash Buffer (10X)
a. Preparation of Working Solution (1X).To prepare 1 liter of Wash Buffer (1X) as an example: Pipette 10 mL of Wash Buffer (10X) into a clean measuring cylinder. Add distilled water, mix, and bring to a final volume of 100 mL. This is now ready-to-use Wash Buffer (1X).Unused prepared Wash Buffer (1X) can be stored at room temperature and is typically stable for 1-2 weeks. For longer storage, keep unused Wash Buffer (1X) at 4°C, where it is typically stable for up to 2 months.Discard the buffer if turbidity or precipitation is observed.
b. Automatic plate washer or manual plate washing: Add 300 μl of washing buffer to each well and allow an interval of 15–30 seconds between dispensing and aspiration. Wash the plate 3–5 times. After the final wash, invert the plate and pat it firmly on thick absorbent paper to dry completely. Proceed with subsequent steps.If the signal value of blank wells in the ELISA remains high under the above washing conditions, appropriately extend the washing time and increase the number of washing cycles. Generally, extending the washing time or increasing the washing frequency will not exert a negative impact on the ELISA results.
4. Color Development Solution
Prepare the working solution by mixing Components A, B at 1:1 volume ratio.
After incubation with SA-HRP or other HRP-conjugated antibodies, wash the plate 3-5 times with Wash Buffer (1X).After the final wash and removal of buffer, add 100 µL of the prepared Color Development Solution per well.ncubate at room temperature for 5-30 minutes, or until the desired color intensity is achieved.Note: This product reacts rapidly. The incubation time can be shortened if necessary.
5. Stop Solution
Use directly without dilution or reconstitution.Add 100 µL of Stop Solution per well to terminate the reaction.Read the absorbance promptly thereafter. The absorbance typically remains stable for up to 1 hour after stopping the reaction.
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