Immunochromatography quantitative detection test paper strip for procalcitonin of terminal blood
A technology of procalcitonin and immunochromatography, which is applied in the field of immunoassay, can solve problems such as difficulty in meeting the minimum sample size of test strips, inability to accurately detect PCT content in peripheral blood, and small amount of peripheral blood sampling, so as to achieve reliable diagnosis Results, beneficial to popularization, and the effect of improving the stability of detection
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Embodiment 1
[0020] Embodiment 1, calcitonin immunochromatographic quantitative detection test strip 1
[0021] Such as figure 1 As shown in the procalcitonin immunochromatographic quantitative detection test strip, the bottom plate 4 is provided with a sample pad 1 , a nitrocellulose membrane 2 and an absorbent pad 3 in sequence. Biotin-labeled PCT monoclonal antibody (concentration: 0.3~1.5mg / mL) and streptavidin-labeled (or avidin) fluorescent protein (using excitation wavelength 530nm and emission wavelength 570nm) were immobilized on sample pad 1 , concentration 0.1~1.0mg / mL); the test line T (concentration 0.5~3mg / mL) composed of a monoclonal antibody recognizing another epitope of PCT immobilized on the nitrocellulose membrane 2 and goat anti-mouse IgG polyclonal antibody Quality control line C (concentration 0.2~2.0mg / mL), quality control line C is used to test the validity of the test strip. The fluorescent protein is one of green fluorescent protein, phycobiliprotein, and the l...
Embodiment 2
[0023] Embodiment two, calcitonin immunochromatography quantitative detection test strip 2
[0024] Compared with the first embodiment, the second embodiment has the following characteristics: the sample pad 1 is composed of a glass cellulose film and a polyester film; anti-human red blood cell antibodies are added to the sample pad 1 .
Embodiment 3
[0025] Embodiment 3. Improvement of Calcitonin Immunochromatography Quantitative Detection Test Strip I
[0026] Such as image 3 As shown, the following improvements are made on the basis of the test strip in Example 2: the sample pad 1 includes a laminated first sample pad 10 and a second sample pad 11, and one end of the first sample pad 10 is placed on the sample pad 1 Below, the second sample pad 11 is overlapped and pressed on one end of the nitrocellulose membrane 2 .
[0027] Further, a positioning bar 12 is set at the end of the first sample pad 10 inserted below the sample pad, and a positioning groove capable of accommodating the positioning bar 22 is provided on the lower end surface of the sample pad 1 .
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