Detection chip and use method thereof
A detection chip and detection layer technology, applied in biochemical equipment and methods, specific-purpose bioreactors/fermenters, biochemical instruments, etc., can solve problems such as the inability to evaluate multiple samples at the same time, and the inability to evaluate the function of a single islet. Achieve the effect of eliminating liquid flow stagnation, increasing shunt entry, and improving detection efficiency
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Embodiment 1
[0066] This embodiment provides a detection chip, and the detection chip is composed of a detection layer and a carrier plate.
[0067] Such as figure 1 As shown, the detection layer includes a sequentially connected sampling section 1, a reaction section 2 and a sampling section 3, wherein:
[0068] The sample injection section includes four sample inlets 16 with a diameter of 1.4mm, which are divided into two groups on average. The four first gradual change channels 11 are connected one by one to each of the four sample inlets 16. The width of the first gradual change channels 11 is determined by 0.68mm is gradually reduced to 0.13mm, and the angle between the two first gradient channels 11 connected to each group of sample inlets 16 is 120°. After the first gradual transition channels 11 converge, it becomes a serpentine channel 12 with a diameter of 0.1mm A gas storage cavity 14 is set at the end of the serpentine channel 12, and a plurality of sub-injection channels 15 w...
Embodiment 2
[0077] Example 2: Experimental comparison of whether the four sample outlets of the chip can output liquid and the difference in the amount of liquid output
[0078] Whether the four sample outlets of the chip provided by Comparative Example 1 and the chip provided by Comparative Example 1 (the pipeline has no gradient) can simultaneously output liquid and the difference in the amount of liquid at low flow rates, when the flow rates of the inlets are respectively 800μL / min, 400μL / min, 200μL / min and 40μL / min, theoretically the corresponding flow rate of a single sample outlet among the four sample outlets is 200μL / min, 100μL / min, 50μL / min and 10μL / min respectively.
[0079] The method is as follows: inject deionized water into the injection port at a flow rate of 800 μL / min, 400 μL / min, 200 μL / min, and 40 μL / min, and the injection volume is 400 μL, and check whether the four sample outlets can simultaneously output samples, Sample flow rate and sample volume, the results are sh...
Embodiment 3
[0092] This embodiment provides a method for detecting the secretory function of a single pancreatic islet by using the detection chip of Embodiment 1.
[0093] (1) Manually select a single islet differentiated from stem cells and put it into the reaction pool of the secretory function detection chip in Example 1, and seal the reaction pool;
[0094] (2) first feed KRB solution containing 2mM glucose and incubate for one hour, then continuously feed KRB solution containing 2mM glucose, KRB solution containing 20mM glucose, KRB solution containing 2mM glucose and KRB solution containing 2mM glucose and 30mM potassium chloride KRB solution was used for 30 minutes each, the flow rate of the injection port was 10 μL / min, and samples were collected every 6 minutes.
[0095] (3) The sample is collected through the sample outlet;
[0096] (4) The insulin concentration in the sample was determined by using the human islet detection kit (Ultrasensitive Insulin ELISA Jumbo, brand: Alpc...
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Abstract
Description
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Application Information
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