Diagnostic Kit for Antibody to Thyroid peroxidase
Production information
Model Number | TPO-IgG/IgM | Packing | 25 Tests/ kit, 30kits/CTN |
Name | Diagnostic Kit for Antibody to Thyroid peroxidase | 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
Thyroid-specific peroxidase (TPO) is synthesized in the endoplasmic reticulum, where it is folded to its native state and undergoes core glycosylation, before being transported to the apical plasma membrane of thyrocytes. In synergy with thyroglobulin (Tg), thyroid-specific peroxidase (TPO) has an essential function in the iodination of L-tyrosine and the chemical coupling of the resulting mono- and diiodotyrosine to form the thyroid hormones of T4, T3, and rT3. TPO is a potential autoantigen. Elevated serum titers of antibodies to TPO are found in several forms of thyroiditis caused by autoimmunity.
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 antibody to thyroid peroxidase (TPO-Ab) in human whole blood, serum, and plasma sample, which’s suitable for auxiliary diagnosis of autoimmune thyroid diseases. This kit only provides test results of antibody to thyroid peroxidase (TPO-Ab), and results obtained shall be used in combination with other clinical information for analysis. 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
