A method and system for simulating macrophages to improve acute kidney injury experiments in mice
A technology of acute kidney injury and macrophages, applied in the field of experimental teaching, can solve the problems of high cost, time-consuming reproduction, inconvenient teaching of popular science, etc., and achieve the effect of improving experimental skills, improving sense of substitution, and reducing experimental errors
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[0051] S2.5, formulate and identify the steps of the induced differentiation product.
[0055] CD86 and CD206 are markers for M1 and M2 macrophages, respectively. The results of flow phenotyping showed that: M0 and M2
[0065] After both kidneys were continuously clamped for 30 min, the arterial clamp was removed.
[0067] S3.3, simulate the experimental process of constructing ischemia-reperfusion-induced acute kidney injury model.
[0080] S5, obtain the pathological tissue detection data of the mouse sample, and provide an experimental summary.
[0081] Specifically, the pathological tissue detection data of the mouse sample is displayed by means of pictures, audio and text.
[0087] M2 promotes metatubular regenerative repair in ischemia-reperfusion-induced acute kidney injury.
[0094] M2 promotes hypoxia-reoxygenation-induced proliferation of mouse primary renal tubular epithelial cells.
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