A vector for introducing a desired gene into a plant, which comprises the desired gene and at least one morphological abnormality induction (MAI) gene as a marker gene, or which comprises the desired gene, at least one MAI gene and a removable element.
A cloned DNA that codes for a plant-derived phospholipase D, and a cloned DNA that controls the expression of a plant-derived phospholipase D gene.
A fused gene has been prepared which comprises the streptavidin gene fused to a gene encoding the human LDL receptor.
Among the ORFs thus obtained, a gene homologous with a known GPCR gene (preferably a gene showing the highest homology with a GPCR gene or a GPCR-associated gene in homology searching) is searched for.
The fusion gene to be detected includes a fusion gene between an ALK gene and another gene.
For example, for the gene that determines eye color, you may inherit a brown allele from your mother and a blue allele from your father.
Sickle Hemoglobin-D Disease: Through research, hemoglobin D, which is a different substitution of the beta globin gene, has been found to interact with the sickle hemoglobin gene.
A recombinant DNA segment which contains a SUC2 promoter linked to an interferon gene for directing the expression of the gene within a yeast cell.
OXA-48: Family of Oxacillinase-48 (Class D) genes.
OXA-48: Family of Oxacillinase-48 (Class D) genes.
Encompassed by the invention is also a method for diagnosing a mutation in an isocitrate dehydrogenase (IDH) gene or in a (D)-2- hydroxyglutarate (D2HG) dehydrogenase enzyme gene in a subject.
For example, for the gene that determines eye colour, you may inherit a brown-eye gene from your mother and a blue-eye gene from your father.
Still further, methods to identify a D. melanogaster gene which modifies the function of, and/or functions in a signaling pathway with an insulin-like gene are provided.
Large deletions
The gene being assayed for in the bodily sample is the TGFB-4 gene (hereinafter referred to as the endometrial bleeding associated factor (ebaf) gene).
A bacterial hemoglobin (Vitreoscilla hemoglobin) gene and a D-amino acid oxidase gene are fused to each other by PCR and the fused DNA fragment is cloned and expressed in E. coli.
To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product.
The elements are associated with a fructose 1,6-bisphosphatase gene, a chlorophyll a/b binding protein gene, a ubiquitin gene, a nopaline synthase gene, and/or a heat shock gene.
The markers are based upon the presence or absence of polymorphisms in the pig estrogen receptor gene.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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