Abstract: The present application relates to a test strip process device. The test strip process device includes an inner cylinder, an outer cylinder, a mounting cover and a liquid supply assembly. One end of the outer cylinder is open, and the other end of the outer cylinder is closed. Both ends of the inner cylinder are open, and the inner cylinder is located in the outer cylinder. An end of the inner cylinder away from the open end of the outer cylinder is hermetically connected to the inner side wall of the outer cylinder, and a test strip chamber is formed between an outer peripheral wall of the inner cylinder and an inner peripheral wall of the outer cylinder. The mounting cover is detachably connected to an end wall of the open end of the outer cylinder, and the liquid supply assembly is provided on the mounting cover.

Abstract: The present application relates to a test strip process device. The test strip process device includes an inner cylinder, an outer cylinder, a mounting cover and a liquid supply assembly. One end of the outer cylinder is open, and the other end of the outer cylinder is closed. Both ends of the inner cylinder are open, and the inner cylinder is located in the outer cylinder. An end of the inner cylinder away from the open end of the outer cylinder is hermetically connected to the inner side wall of the outer cylinder, and a test strip chamber is formed between an outer peripheral wall of the inner cylinder and an inner peripheral wall of the outer cylinder. The mounting cover is detachably connected to an end wall of the open end of the outer cylinder, and the liquid supply assembly is provided on the mounting cover.

Abstract: The present invention discloses a CRISPR/LpCas9 gene editing system and application thereof, the CRISPR/LpCas9 gene editing system includes a complex of LpCas9 protein and sgRNA, which can accurately locate a target DNA sequence and cleave DNA double strands. The LpCas9 protein has an amino acid sequence shown in SEQ ID NO:1; and the sgRNA has a nucleotide sequence shown in SEQ ID NO:2, or a modified sgRNA sequence based on SEQ ID NO: 2. The present invention can effectively solve the problems of heterologous codon bias and cytotoxicity in the application of SpCas9 in Lactobacillus paracasei. The gene editing is performed in cells or in vitro by introducing artificially designed CRISPR RNA and a repair template, which solves the problem of low electroporation efficiency caused by the strains' characteristics or relatively large carried plasmids, and has broad application prospects in the field of gene editing.

Abstract: A light guide plate, a backlight module and a display device are provided. The light guide plate comprises at least one light incident surface having at least one first light incident surface, a light emitting surface adjacent to the light incident surface, and a plurality of lateral faces adjacent to the light emitting surface. At least one lateral face adjacent to the light emitting surface is disposed with a plurality of reflective microstructures.

Abstract: The present invention relates to a novel hyaluronan receptor protein involved in cell locomotion or motility and in cell proliferation and transformation and to DNA sequences encoding this protein. The protein is designated Receptor for Hyaluronic Acid Mediated Motility or RHAMM.