Reagent device and method for detecting anti-Jo-1 antibody

Abstract

The invention provides a reagent device and a method used for detecting anti-Jo-1 antibodies. The reagent device has a long strip shape, and has a base body comprising 8 hole positions and a handle positioned on one end of the base body. From the end proximal to the handle, the 8 hole positions are sequentially a sample hole, an auxiliary agent hole, an enzyme conjugate hole, a substrate hole, a termination liquid hole, a dilution liquid hole, a reaction hole, and a dilution hole. According to the invention, based on a principle of enzyme-linked immunoassay, anti-Jo-1 antibody is detected by using the reagent device. The method is an independent single-person analysis and detection method. The device can be used in cooperation with a corresponding specific analysis instrument. During a detection process, detection reagents or samples are injected by using a full-automatic precise dosing device. The device and the method have the advantages of automatic operation, precise dosing, high detection result accuracy, high detection result precision, and wide application prospect.

Description

technical field [0001] The application of the present invention relates to a reagent device and method for detecting anti-Jo-1 antibody, belonging to the technical field of clinical immunology detection. Background technique [0002] Primary polymyositis is a systemic disease that usually starts insidiously and progresses slowly over weeks, months, or years. Patients may have morning stiffness, fatigue, loss of appetite, weight loss, fever, and joint pain , a small number of patients have Raynaud's phenomenon. The incidence of this disease can reach one million people every year, and the male to female incidence ratio is 1:3. The age of onset is mostly in two stages of 10-14 years old or 45-50 years old. [0003] Jo-1 antibody is a kind of histidyl-tRNA synthetase antibody. This cytoplasmic enzyme catalyzes the esterification reaction of histidine and tRNA, which exists in the form of homodimer in the cytoplasm, and the molecular weight of the subunit is about 50kD. The e...

AI Technical Summary

Problems solved by technology

[0007] (1) Only qualitative and semi-quantitative analysis can be carried out, and the specific amount of the tested substance cannot be obtained

[0008] (2) The operation steps are cumbersome and the test takes a long time

[0009] (3) The detection sensitivity needs to be improved

[0014] (1) Non-specific recognition cannot be distinguished according to the size of the molecular weight when analyzing the results;

[0015] (2) The operation is relatively complicated and requires expensive fluorescence microscopes, which are difficult to popularize in many primary hospitals and are not suitable for laboratories with a large number of specimens;

[0016] (3) The background in the fluorescence measurement is relatively high, and it is difficult to use the fluorescence immunoassay technique for quantitative determination;

[0017] (4) Experienced professionals are required to determine the results, and the objectivity of the analysis results is insufficient;

[0018] (5) Only qualitative detection can be carried out, and quantitative measurement cannot be carried out

[0021] (1) Use 12×8 type, 6×8 type, 8×12 type or full-plate type 96-well special microwell plate as antigen coating equipment and reaction container, which can only be divided into 12 batches and 6 batches when used , 8 batches or the whole board can be used at one time, and independent and single-person testing cannot be carried out;

[0022] (2) There are many kinds of reagents used in quantitative determination, and each detection reagent must be contained in a reagent bo...

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