Mumps virus enzyme-linked assay kit
A mumps virus and detection kit technology, applied in the biological field, can solve problems such as uneven quality, high price, and restrictions on widespread use, and achieve high consistency, broad application prospects, and good specificity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0027] Such as figure 1 and figure 2 As shown, a mumps virus enzyme-linked detection kit provided by the present invention includes a box body (15), 8 concave bottle positions (4) built in the box body, 8 bottles of reagent bottle sets, and an enzyme-labeled reaction plate (1) Three sheets of plate sealing film (3) The 8 concave bottle positions are respectively placed with sample diluent (8), enzyme marker (11), concentrated washing solution (12), substrate Solution A (9), Substrate Solution B (7), Stop Solution (5), Negative Control (6), Positive Control (10) each bottle, the enzyme-labeled reaction plate is located behind the reagent bottle, the The sealing film is adjacent to the enzyme-labeled reaction plate; and the size of the sealing film is the same as that of the enzyme-labeled reaction plate; the enzyme-labeled reaction plate includes a support frame (13), and is placed on the support frame There are several detachable micro-well reaction strips (16); 96 micro-re...
Embodiment 2
[0066] Example 2: Using the above kit to detect mumps IgG antibodies in serum by ELISA
[0067] 1. Before the experiment, take the kit out of the refrigerator and leave it at room temperature for 30 minutes before use;
[0068] 2. Dilute the concentrated washing solution 20 times with distilled water before use;
[0069] 3. For each test, set 1 well for positive control and negative control, add 100ul of control solution to each well; 1 blank well (no serum sample diluent, sample and enzyme-labeled antibody, only add substrate A, B and stop solution) ; The rest are sample wells, add serum sample diluent 100ul and sample 1ul to each well. Paste the parafilm and incubate at 37°C for 30 minutes;
[0070] 4. Discard the liquid in the well, pat dry, add 350ul of washing solution to each well, let it stand for 5-10 seconds, discard, pat dry, repeat washing 5 times, and pat dry;
[0071] 5. Add 100ul of enzyme markers, stick a parafilm, and incubate at 37°C for 30 minutes;
[007...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 