Product Specification

                             Anti-ANA IgG ELISA Test Kit

Drug Names

Generic Name:Anti-ANA IgG ELISA Test Kit

INTENDED USE

This kit is a qualitative detection of human serum/plasma of Anti-nuclear IgG antibody. The kit is suitable for clinical screening and diagnosis. Manydiseases may cause anti-nuclear antibody positive results, lupus erythematosus (SLE) is the most common disease. And anti-nuclear antibody can also be found in drug induced lupus erythematosus, overlap syndrome, mixed connective tissue disease, systemic scleroderma, dermatomyositis, sjogren syndrome (SS), rheumatoid arthritis, autoimmune hepatitis (lupoid hepatitis), Hashimoto's thyroiditis (chronic thyroiditis) and myasthenia gravis.

Product details

PRINCIPLE

This kit uses indirect ELISA principle to detect ANA IgG. Purified ANA antigen is pre-coated on the microplate, the anti-nuclear IgG antibody in sample will combine with ANA antigen first, then combine with enzyme-labeled second antibody to form antigen-antibody-anti-antibody complex, and show blue color in the microplate. This kit is used for the specific detection of ANA IgG in human serum/plasma.

TEST PROCEDURE

1. All reagents should be allowed to reach room temperature for 15 minutes before use.

2. Dilute the wash buffer at the rate of 1:40 dilution with distilled water before use.

3. Add 100μL Sample Diluent in the corresponding well, add 5μL sample in the corresponding well (Do not add in the blank well). Mix thoroughly by the pipette. Add 50μL of positive control and cut-off control to the positive control well and cut-off control well. The sample should be corresponding to the number of micro plate, each plate should be provided with cut-off control 2 wells, positive control 1 well and blank control 1 well. Note: Use a separate disposal pipette tip for each specimen, Cut-off and Positive Control to avoid cross-contamination.

4. Shake gently to mix for 30s. Incubate at 37°C for 20 minutes with the sealing plate membrane sealing the plate.

5. At the end of the incubation, remove and discard the plate cover. Take out, add wash buffer to each well for 20 seconds. Repeat 5 times. After the final washing cycle, turn the plate over onto blotting paper or clean towel, and tap it to remove any remainders.

6. Respectively adding Conjugate 50μL (Do not add in the blank well)

7. Incubate at 37°C for 20 minutes with the sealing plate membrane sealing the plate. Repeat the wash step for 5 times as in step 5.

8.Add Substrate A 50µL and Substrate B 50µL (Do not add in the blank well). Incubate at 37°C for 10 minutes with the sealing plate membrane sealing the plate.

9. Add 50μL Stop Solution to each well (Do not add in the blank well). Mix gently by shaking, read the absorbance within 10 minutes after stopping the reaction. Calibrate the plate reader with the Blank well and read the absorbance at 450nm.If a dual filter instrument is used, set the reference wavelength at 630nm. Set no blank wells is allowed if use dual wavelength to detect. Calculate the Cut-off value and evaluate the results.

Important notes

• The kit takes out from the refrigeration environment should be balanced 15-30 minutes in the room temperature then use, ELISA plates coated if has not use up after opened, the plate should be stored in Sealed bag.
• washing buffer will Crystallization separation, it can be heated the water helps dissolve when

dilute . Washing does not affect the result.

• add Sample with sampler Each step, And proofread its accuracy frequently, avoids the experimental error. add sample within 5 min, if the number of sample is much , recommend to use Volley .
• Please make specification curve when you assay, had better make duplicate well, if in the sample the testing material content is excessively high (The sample OD is bigger than the first standard well OD ),please use Sample dilution to dilute certain multiple (n times),then assay. Please multiply total Dilution Times when calculate(×n×5).
• Closure plate membrane only limits the disposable use, in order to avoid the overlapping pollution.
• The substrate please evade the light preservation.
• Please according to use instruction strictly, The test result determination must take the microtiter plate reader as a standard .
• All samples, washing buffer and each kind of reject should according to infective material process.
• This reagent which different batch number component do not mix.
• If it’s different form English instruction, take English instruction as the standard.

Storage and stability

• Store at 2-8℃.

• Seal and return unused reagents to 2-8℃, under which conditions the stability will be retained for 2 months, or until the labeled expiry date, whichever is earlier.