ã€Precautions】 [Limitations of inspection methods] The non-invasive/high-flow integrated ventilator (BPAP-HE) is a non-invasive ventilator, a high-flow respiratory humidifier, or a high-performance humidifier. BPAP HE,Non Invasive Vent,Niv Breathing Machine,Non Invasive Ventilation Machine Shenyang RMS MEDICAL TECH CO.,LTD , https://www.medicalrms.com
[Package Specification] 24 person/box 48 person/box [intended use] for detecting genital mycoplasma antibody (IgM/IgG) in test serum
[Test principle] Using the genital mycoplasma antigen solid phase nitrocellulose membrane, the principle of percolation indirect method is applied to detect the genital mycoplasma antibody in serum.
[main components]
Reaction plate 24 parts or 48 parts reagent I 1 bottle 0.02mol/L PH 7.4 PBS
Reagent II 1 bottle of colloidal gold label [Storage conditions and expiration date] The product should be stored in the condition of 2 ° C ~ 8 ° C, can not be frozen; effective period of 24 months.
[sample requirements]
Serum samples should not be hemolyzed and should be stored in fresh serum or at 2 ° C ~ 8 ° C for no more than one week.
Hyperlipidemia serum cannot be used.
ã€Testing method】
Drop two drops of reagent I into the central well of the reaction plate, to be completely infiltrated;
100 μl of serum was instilled into the wells of the reaction plate until completely infiltrated;
Add three drops of reagent II to the well of the reaction plate, to be completely infiltrated;
Three drops of reagent I were infiltrated into the wells of the reaction plate to be completely infiltrated.
[product performance indicators]
In-batch precision: positive coincidence rate and negative coincidence rate should be ≥95%, and the depth of reaction spots should be close.
Inter-assay precision: positive coincidence rate and negative coincidence rate should be ≥95%.
This product has not yet obtained the product registration number, only for research, without clinical diagnosis.
Once the test is started, it should be carried out continuously according to the operation steps until the end.
When the kit is removed from the refrigerator, the reagent should be returned to room temperature.
This reagent test is only used to detect genital mycoplasma antibodies rather than directly detecting genital mycoplasma antigens, so the positive result is not confirmed to be a Mycoplasma genitalium infection. The diagnosis of the patient's condition should be combined with a comprehensive analysis of the patient's clinical signs and symptoms and test results.
It is possible that serum samples with low antibody content cannot be detected. Some patients with genital mycoplasma infection do not produce antibodies or produce small amounts of antibodies. At this point, a negative result may be displayed.
When the test results are suspicious, the culture method is used to confirm the diagnosis.
The non-invasive ventilator mode of this product can be used for adult patients who do not rely on invasive ventilation support, such as respiratory dysfunction, to provide ventilation assistance and respiratory support;
Products with high-flow heating and humidification mode can be used for humidification and oxygen therapy for adult patients with spontaneous breathing.
Protozoa mycoplasma antibody elisa detection kit instructions
Detailed introduction:
[product name] genital mycoplasma antibody detection kit (colloidal gold method)