Schistosoma circulating antigen detection kit (colloidal gold method)
Description book

[Product name] Schistosoma circulating antigen detection kit (colloidal gold method)
[Packing specifications] 24 servings / box 48 servings / box [Expected use] Used to detect schistosomiasis circulating antigen in test serum.
[Test principle] Use schistosomiasis monoclonal antibody solid phase nitrocellulose membrane and apply the principle of diafiltration indirect method to detect schistosomiasis circulating antigen in serum.
[Main components]
1. 24 or 48 reaction plates
2. Reagent â…  1 bottle of 0.02mol / L PH 7.4 PBS
3. Reagent Ⅱ 1 bottle of colloidal gold marker [storage conditions and expiration date] The product should be stored at 2 ℃ ~ 8 ℃ conditions, can not be frozen; the expiration date is 24 months.
[Sample requirements]
1. Serum samples cannot be hemolyzed, and should be stored in fresh serum or stored at 2 ℃ ~ 8 ℃ for no more than one week.
2. Hyperlipidemia serum cannot be used.
【Testing method】
1. Drop two drops of reagent â…  into the central hole of the reaction plate and wait for complete infiltration;
2. Drip 100µl of serum into the well of the reaction plate, to be completely infiltrated;
3. Add three drops of reagent â…¡ to the well of the reaction plate until it is completely infiltrated;
4. Infiltrate three drops of reagent â…  into the well of the reaction plate and wait for complete infiltration.
[Interpretation of results]
Positive: Red round spots appear on the C end and red round spots on the T end of the reaction plate well, which is positive for schistosomiasis circulating antigen;
Negative: There are red round spots on the C-end and no red round spots on the T-end of the reaction plate well, which is negative for schistosomiasis circulating antigen.
Failure: No red round spots appear on the C-end of the reaction plate well, or no red round spots appear on the C-end and T-end.
[Limitations of inspection methods]
1. This reagent test is used to detect schistosomiasis circulating antigen. The diagnosis of the patient's condition should be combined with the patient's clinical signs and symptoms and the comprehensive analysis of the test results.
2. It is possible that serum samples with low antigen content cannot be detected. At this time, a negative result may be displayed.
3. When the test result is suspicious, use other methods to confirm the diagnosis.
【Product Performance Index】
1. In-batch precision: both the positive coincidence rate and the negative coincidence rate should be ≥95%, and the color depth of the reaction spots should be close.
2. Precision between batches: Both the positive and negative coincidence rates should be ≥95%.
【Precautions】
1. This product has not yet obtained a product registration certificate number, which is for research only and does not require clinical diagnosis.
2. Once the test is started, it should be carried out continuously according to the operation steps until the end.
3. When the kit is removed from the refrigerator, the reagents should be returned to room temperature.

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PRODUCT DESCRIPTION

                                              Design:  Customized Design

                                              Size:       295mm×140mm×100mm
                                                             285mm×140mm×100mm               

                                                             240mm×110mm×85mm

                                               Paper:   Food-grade Greasproof Brown Kraft Paper

                                               Compound Adhesive: Water-based White Adhesive PVA 

                                               Heat Seal Adhesive: PVA Water Soluble (Green)

                                               Side Seam Adhesive: Water Soluble Emulsion(White) 

                                               Ink: MWW (M/W Water Base Carbon Free) 

                                               Individual weight: 11.2g

                                               Oil resistant: â‰¥  kit11

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