Products/Services Used | Details | Operation |
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PCR Cloning and Subcloning> | DNA from resistant plants was collected and stored using Whatman™ FTA™ paper (GE Healthcare; gehealthcare.com) and genotyped using Genscript Taq polymerase and a combination of vector and insert-specific primers (Supplementary Table 1).Genscript Taq polymerase (Genscript; genscript.com) was used for PCR. The second round PCR products were shotgun cloned using the TOPO®-TA system (Thermo-Fisher Scientific). Individual clones were isolated, plasmids extracted (Plasmid Extraction Kit, BioBasic; store.biobasic.com) and the inserts sequenced (Genscript; genscript.com) using universal vector primers. | Get A Quote |
The Arabidopsis seed coat-specific promoter fragment described is an important tool for basic and applied research in Brassicaceae species. During differentiation, the epidermal cells of the Arabidopsis seed coat produce and secrete large quantities of mucilage. On hydration of mature seeds, this mucilage becomes easily accessible as it is extruded to form a tightly attached halo at the seed surface. Mucilage is composed mainly of pectin, and also contains the key cell wall components cellulose, hemicellulose, and proteins, making it a valuable model for studying numerous aspects of cell wall biology. Seed coat-specific promoters are an important tool that can be used to assess the effects of expres... More