Blood Quantitative Total IgE FIA test kit
Production information
| Model Number | Total IgE | Packing | 25 Tests/ kit, 30kits/CTN |
| Name | Diagnostic Kit for Total IgE | Instrument classification | Class II |
| Features | High sensitivity, Easy opeation | Certificate | CE/ ISO13485 |
| Accuracy | > 99% | Shelf life | Two Years |
| Methodology | Fluorescence Immunochromatographic Assay |
OEM/ODM service | Avaliable |
Summary
Immunoglobulin E (IgE) is the least abundant antibody in serum .The concentration of IgE in serum is associated with age, with the lowest values being measured at birth. Generally，adult lgE leavels are avhieved by 5 to 7 years of age .Between the ages of 10 and 14 years, IgE levels may be higher than those in adults. After age 70 years, IgE levels may decline slightly and be lower than the levels observed in adults younger than 40 years.
However, the normal level of IgE cannot exclude allergic diseases. Therefore, in the differential diagnosis of allergic and non-allergic diseases, quantitative detection of human serum IgE level is only of practical significance when used in combination with other clinical tests.
Feature:
• High sensitive
• result reading in 15 minutes
• Easy operation
• Factory direct price
• need machine for result reading
Intended Use
This kit is applicable to in vitro quantitative detection of Total Immunoglobulin E (T-IgE) in human serum/plasma/whole blood samples and used for Allergic diseasea. The kit only provides test result of Total Immunoglobulin E (T-IgE). The obtained result shall be analyzed in combination with other clinical information. It must only be used by healthcare professionals.
Test procedure
| 1 | Use of portable immune analyzer |
| 2 | Open the aluminum foil bag package of reagent and take out the test device. |
| 3 | Horizontally insert the test device into the slot of immune analyzer. |
| 4 | On home page of operation interface of immune analyzer, click “Standard” to enter test interface. |
| 5 | Click “QC Scan” to scan the QR code on inner side of the kit; input kit related parameters into instrument andselect sample type.Note: Each batch number of the kit shall be scanned for one time. If the batch number has been scanned, then skip this step. |
| 6 | Check the consistency of “Product Name”, “Batch Number” etc. on test interface with information on the kit label. |
| 7 | Start to add sample in case of consistent information:Step 1: take out sample diluents, add 80µL of serum/plasma/whole blood sample, and mix well
Step 2: Add 80µL of above mixed solution into the sample hole of test device. Step 3: After complete sample addition, click “Timing” and remaining test time will be automatically displayed on the interface |
| 8 | After complete sample addition, click “Timing” and remaining test time will be automatically displayed on theinterface. |
| 9 | Immune analyzer will automatically complete test and analysis when test time is reached. |
| 10 | After test by immune analyzer is completed, test result will be displayed on test interface or can be viewed through“History” on home page of operation interface. |
Factory
Exhibition
