An antibody chip kit for diagnosis of various tumors
A technology of antibody chips and kits, applied in the field of biomedicine, can solve the problems of single detection index, cumbersome operation, low sensitivity, etc., and achieve the effect of optimized dot matrix, uniform distribution, and easy operation
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Embodiment 1
[0024] Example 1: Determination of antibody chip spotting conditions.
[0025] 1. Spotting concentration of the capture antibody: put the capture antibody in different buffers (sterile water, PBS buffer, PBS containing different concentrations of bovine albumin, PBS buffer containing different concentrations of glycerol, etc.) at a concentration of 2x Dilute it, spot it on the surface of the chip with a non-contact spotter, and compare its activity and stability with a sandwich ELISA method. Experiments show that diluting the capture antibody with PBS buffer containing 0.01-10g / 100ml bovine albumin has the best linear rate and stability.
[0026] 2. Condition control of spotting: when the capture antibody is directly spotted on the surface of the slide at room temperature, the spot of the capture antibody is likely to produce hollow spots, and the activity of different antibody spots is quite different, and it is often found that there will be some spots in the final generated...
Embodiment 2
[0027] Example 2: Preparation of the antibody chip kit for diagnosis of various tumors according to the present invention.
[0028] In order to detect whether there are corresponding tumor markers in the sample, prepare slides immobilized with specific antibodies against the following tumor markers: alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), cancer antigen CA125, cancer antigen CA19 -9, cancer antigen CA153, prostate-specific antigen (fPSA and tPSA), neuron-specific enolase (NSE), calcitonin (PCT), iron-binding protein (Ferritin), β2-microglobulin (beta2- Microglobin), beta human chorionic gonadotropin (HCGb), pepsinogen (Pepsinogen1 and 2), thyroglobulin (Thyroglobulin), prolactin (Prolactin) and human epididymis secretory protein 4 (HE4).
[0029] 1. The source of the antibody:
[0030] Specific antibodies against the proteins listed in Table 1 were used, and the use, source, and concentration of the antibodies are detailed in Table 1. All detection antibodie...
Embodiment 3
[0042] Example 3: An experiment of quantitative detection of tumor markers using the kit of the present invention.
[0043] 1. Complete drying of the slide chip
[0044] Take the slide chip out of the box, and after equilibrating at room temperature for 20-30 minutes, open the packaging bag, peel off the sealing strip, and then place the chip in a vacuum desiccator or dry at room temperature for 1-2 hours.
[0045] 2. Gradient dilution of tumor marker standards
[0046] 2.1 Add 500 μl of sample diluent to the vial of the tumor marker standard mixture and redissolve the standard. Before opening the vial, give it a quick centrifuge and gently pipet up and down to dissolve the powder. Label this vial as Std1.
[0047] 2.2 Mark six clean centrifuge tubes as Std2, Std3 to Std7 respectively, and add 200 μl of sample diluent to each small tube.
[0048] 2.3 Take 100 μl of Std1 and add it to Std2 and mix gently, then take 100 μl from Std2 and add it to Std3, and then dilute it to S...
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