Pathogen treatments were performed using 4-week old plants that were syringe-infiltration with Psm ES4326/avrRpm1 (OD600nm = 0.1), spray inoculated with Pst DC3000 (OD600nm = 0.2, 0.02% Silwet L-77) or Pst DC3118 (OD600nm = 0.2, 0.02% Silwet L-77). Untreated root, shoot leaf, shoot, and flower tissues were collected to determine the basal levels of tarnscripts. We extracted total RNA from the collected samples using RiboZol (AMRESCO). Possible genomic DNA contamination was eliminated using DNase I (Ambion). Formaldehyde agarose gel preparation, quantification, electrophoresis and samples prepration/loading were done following the RNeasy Plant Mini® Kit QIAGEN protocol. SuperScript III first-strand RT-PCR kit (Invitrogen) was used to convert mRNA into cDNA. We used GoTaq qPCR Master Mix (Promega) to perform qRT-PCR using gene-specific primers in a RealPlex S MasterCycler (Eppendorf). Primers used in this study are listed in the Supplementary Table 1.
Elf18
Elf18 is a lab equipment product manufactured by GenScript. It serves as a tool for researchers and scientists in their laboratory work. The core function of Elf18 is to provide a reliable and accurate measurement of various parameters in the laboratory environment.
Lab products found in correlation
2 protocols using elf18
Arabidopsis Immune Response to Pathogens
Pathogen treatments were performed using 4-week old plants that were syringe-infiltration with Psm ES4326/avrRpm1 (OD600nm = 0.1), spray inoculated with Pst DC3000 (OD600nm = 0.2, 0.02% Silwet L-77) or Pst DC3118 (OD600nm = 0.2, 0.02% Silwet L-77). Untreated root, shoot leaf, shoot, and flower tissues were collected to determine the basal levels of tarnscripts. We extracted total RNA from the collected samples using RiboZol (AMRESCO). Possible genomic DNA contamination was eliminated using DNase I (Ambion). Formaldehyde agarose gel preparation, quantification, electrophoresis and samples prepration/loading were done following the RNeasy Plant Mini® Kit QIAGEN protocol. SuperScript III first-strand RT-PCR kit (Invitrogen) was used to convert mRNA into cDNA. We used GoTaq qPCR Master Mix (Promega) to perform qRT-PCR using gene-specific primers in a RealPlex S MasterCycler (Eppendorf). Primers used in this study are listed in the Supplementary Table 1.
Arabidopsis Immune Response Profiling
Total RNA was extracted from collected samples using RiboZol (AMRESCO) and genomic DNA contamination was removed using DNase I (Ambion). mRNA was converted into cDNA using the SuperScript III first-strand RT-PCR kit (Invitrogen). Gene expression analysis was conducted with GoTaq qPCR Master Mix (Promega) using gene-specific primers in a RealPlex S MasterCycler (Eppendorf). Primers used for this study are listed in the Supplementary Table
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