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Table S1

January 2013

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Georgia Institute of Technology

Georgia Institute of Technology

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Primers used to analyze the STMV RNA. (PDF)

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In Vitro Secondary Structure of the Genomic RNA of Satellite Tobacco Mosaic Virus

Article

January 2013

Shreyas S Athavale · J Jared Gossett · Jessica Bowman · Nicholas Hud · Stephen C Harvey

Data

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Table S4

March 2012

Forward and Reverse primer sequences used for QPCR for each target RNA. The list of forward and reverse primers used in this study. (DOCX)

Data

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Figure S4

January 2012

V-ATPase, V-PPase, PM-ATPase Activity and RT-PCR analyses of AtAHA1, AtSOS1, AtAVP1, AtNHX1, AtNHX2 and AtNHX5. Young leaves of 4-week-old plants of Col-0, fad2 and fad2/FAD2 (fad2/FAD2-1) treated with or without 250 mM NaCl for 3 days were used. A-C, Tonoplast and plasma membrane fractions were isolated and enzyme activity assays were performed. D, RT-PCR assays. Total RNA was isolated and ... [Show full abstract] RT-PCR was performed with gene specific primers (Table S1). Expression of ACTIN2 was employed as an internal control. (TIF)

Data

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Supplementary Material 10

August 2015

Table S3. Primers used for RACE, RT‐qPCR and RNA in situ hybridization.

Data

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Figure S3

September 2011

Gene expression of a set of cellulases in a wild type strain (FGSC 2489). A culture of FGSC 2489 was grown for 16 hours in MM-sucrose and subsequently transferred to MM-Avicel. RNA was extracted at different time points (noted above), and subjected to quantitative RT-PCR using primers to an intracellular β-glucosidase (NCU00130) or gh5-1 (NCU00762) or cbh-1 (NCU07340) or gh61-4 (NCU07898) or ... [Show full abstract] gh6-2 (NCU009682) (see Materials and Methods). Primer sequences are listed in Table S1. Expression was normalized to that of the N. crassa actin gene (NCU04173). Expression levels were verified by subsequent microarray analyses. (TIF)