A method for establishing a biological model on joint toxicity of Caenorhabditis elegans and an application thereof are provided. The method for establishing the biological model includes adding the L1-stage Caenorhabditis elegans to a mixed system of working solution of mycotoxins containing tenuazonic acid and penicillin, K-medium solution and E. coli OP50 to obtain L1-stage Caenorhabditis elegans. The biological model indicates that TeA and PAT have a synergistic effect on the growth, development and reproductive ability of Caenorhabditis elegans, and their toxicity mechanism is related to inducing nematodes and stimulating transcriptional factors of Daf-16 genes. The biological model and detection method are simple to operate and its test period is short.

Described are Caenorhabditis elegans (C. elegans) strains exhibiting an RNA toxicity phenotype. The C. elegans strains comprise a detectable reporter gene expressed in one or more cell types, with the expressed reporter gene RNA having in instance of at least fifty oligonucleotide repeats (e.g., trinucleotide repeats). Exemplary C. elegans reporter strains are generated that exhibit phenotypes characteristic of the human disorder Myotonic Dystrophy 1. The C. elegans strains are amenable for high-throughput screening applications, for both gene target as well as small molecule identification.

A cancer detection method characterised in that a nematode is bred in the presence of bio-related material originating from a test subject, or a processed product of same, and cancer is detected using the chemotaxis due to the sense of smell of the nematode as an indicator.

The present disclosure provides transgenic nematode systems for assessing function of heterologous genes, their variants and drug discovery. The transgenic nematodes contain a heterologous gene that is inserted via homologous recombination at the native locus replacing and removing the nematode ortholog, wherein expression of the heterologous gene rescues function of the removed nematode ortholog and a transgenic control animal is provided. The heterologous gene may be further modified to provide a variant, such as a human clinical variant, whereby a transgenic test animal is provided. Those transgenic test animals are used in methods to assess function of the heterologous variant and drug screens to find therapeutic candidates reversing deviant activity back to wildtype.

The present disclosure provides transgenic nematode systems for assessing function of heterologous genes, their variants and drug discovery. The transgenic nematodes contain a heterologous gene that is inserted via homologous recombination at the native locus replacing and removing the nematode ortholog, wherein expression of the heterologous gene rescues function of the removed nematode ortholog and a transgenic control animal is provided. The heterologous gene may be further modified to provide a variant, such as a human clinical variant, whereby a transgenic test animal is provided. Those transgenic test animals are used in methods to assess function of the heterologous variant and drug screens to find therapeutic candidates reversing deviant activity back to wildtype.

The present invention refers to a method for generating a binodal curve of a polymer in a system by determining accurate values of both concentration of dilute and condensed phases of a polymer, in particular, protein or polynucleic acid, under different condition, such as at different temperatures and salt concentrations. Furthermore, the present invention refers to an assay method for identify bioactive compound(s), comprising the inventive method for generating a binodal curve of a polymer in a system.

A cancer detection method characterised in that a nematode is bred in the presence of bio-related material originating from a test subject, or a processed product of same, and cancer is detected using the chemotaxis due to the sense of smell of the nematode as an indicator.

The present invention includes a system and method for analyzing animals including: a media reservoir and a media pump in fluid communication with the media reservoir; a food reservoir and a food pump in fluid communication with the food reservoir; an input port in fluid communication with the media pump and the food pump; a microfluidic device in fluid communication with the input port including: a micropillar arena or a plurality of micropillar chambers; an outlet port in fluid communication with the microfluidic device; a light source positioned outside the micropillar arena to illuminate the interior of the micropillar arena; an imager positioned outside the micropillar arena to image the interior of the micropillar arena; and a controller coupled to the media pump, the food pump, the microfluidic device, the light source, and the imager.