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<title>The Meetingpoint at Slavyanski.net / taxhill37 / Upvoted</title>
<link>https://slavyanski.net/sb2020</link>
<description>Your Source for Social News and Networking</description>
<pubDate>Fri, 28 Aug 2020 07:58:13 +0000</pubDate>
<language>en</language>
<item>
	<title><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-7</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-7"><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></source>
	<description><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 10  [v/v] glycerol, and 1 mg of digitonin) and kept on ice for 30 min. Ten microliters of antibody serum, 50 mL of Protein A-Sepharose, 1  (w/v) BSA, and Complete protease inhibitor (Roche) were added to the mitochondria and incubated for 6 h at 4  on a rotating wheel at 20 rpm. Beads were  ]]></description>
	<pubDate>Fri, 28 Aug 2020 07:58:13 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-7</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Mon, 24 Aug 2020 06:56:14 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-6</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-6"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Fri, 21 Aug 2020 06:57:17 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-6</guid>
</item>

<item>
	<title><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8"><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></source>
	<description><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 10  [v/v] glycerol, and 1 mg of digitonin) and kept on ice for 30 min. Ten microliters of antibody serum, 50 mL of Protein A-Sepharose, 1  (w/v) BSA, and Complete protease inhibitor (Roche) were added to the mitochondria and incubated for 6 h at 4  on a rotating wheel at 20 rpm. Beads were  ]]></description>
	<pubDate>Fri, 21 Aug 2020 06:39:18 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Thu, 20 Aug 2020 12:32:49 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4</guid>
</item>

<item>
	<title><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8"><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></source>
	<description><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 10  [v/v] glycerol, and 1 mg of digitonin) and kept on ice for 30 min. Ten microliters of antibody serum, 50 mL of Protein A-Sepharose, 1  (w/v) BSA, and Complete protease inhibitor (Roche) were added to the mitochondria and incubated for 6 h at 4  on a rotating wheel at 20 rpm. Beads were  ]]></description>
	<pubDate>Thu, 20 Aug 2020 11:33:19 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-9</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-9"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Thu, 20 Aug 2020 11:19:20 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-9</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-2</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-2"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Tue, 18 Aug 2020 12:19:14 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-2</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-3</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-3"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Tue, 18 Aug 2020 11:58:09 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-3</guid>
</item>

<item>
	<title><![CDATA[Es and one proline of the CxxxPxC motif located upstream of]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=es-and-one-proline-of-the-cxxxpxc-motif-located-upstream-of-9</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=es-and-one-proline-of-the-cxxxpxc-motif-located-upstream-of-9"><![CDATA[Es and one proline of the CxxxPxC motif located upstream of]]></source>
	<description><![CDATA[Es and one proline of the CxxxPxC motif located upstream of the CxCxxC clusters did reduce PP2A binding significantly. Additional studies that relied upon peptide inhibition of the tAg-PP2A interaction without destabilizing tAg suggested that the CxCxxC clusters might indeed influence tAg binding to the A subunit [23,25]. Two recent X-ray crystallographic studies indicate the CxCxxC clusters and t ]]></description>
	<pubDate>Mon, 17 Aug 2020 07:52:04 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=es-and-one-proline-of-the-cxxxpxc-motif-located-upstream-of-9</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-7</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-7"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Fri, 14 Aug 2020 12:32:11 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-7</guid>
</item>

<item>
	<title><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8"><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM]]></source>
	<description><![CDATA[Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 10  [v/v] glycerol, and 1 mg of digitonin) and kept on ice for 30 min. Ten microliters of antibody serum, 50 mL of Protein A-Sepharose, 1  (w/v) BSA, and Complete protease inhibitor (Roche) were added to the mitochondria and incubated for 6 h at 4  on a rotating wheel at 20 rpm. Beads were  ]]></description>
	<pubDate>Fri, 14 Aug 2020 11:00:54 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=mitochondrial-pellet-was-resuspended-in-digitonin-buffer-30-mm-hepes-koh-ph-7-4-150-mm-8</guid>
</item>

<item>
	<title><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-5</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-5"><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></source>
	<description><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the reaction, and samples were resolved by SDS-PAGE, dried, and exposed to a phosphor-imaging screen.Plant Material and Growth ConditionsArabidopsis (Arabidopsis thaliana) T-DNA insertional knockout lines for Tric1 (SALK_031707, SALK_112126, and At3g49560) and Tric2 (SALK_136525, SALK_149871, and At5g24650) were obtained from ABRC and sc ]]></description>
	<pubDate>Wed, 12 Aug 2020 18:15:13 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-5</guid>
</item>

<item>
	<title><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7"><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></source>
	<description><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the reaction, and samples were resolved by SDS-PAGE, dried, and exposed to a phosphor-imaging screen.Plant Material and Growth ConditionsArabidopsis (Arabidopsis thaliana) T-DNA insertional knockout lines for Tric1 (SALK_031707, SALK_112126, and At3g49560) and Tric2 (SALK_136525, SALK_149871, and At5g24650) were obtained from ABRC and sc ]]></description>
	<pubDate>Wed, 12 Aug 2020 18:14:43 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-5</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-5"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Tue, 11 Aug 2020 22:00:15 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-5</guid>
</item>

<item>
	<title><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-6</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-6"><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></source>
	<description><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the reaction, and samples were resolved by SDS-PAGE, dried, and exposed to a phosphor-imaging screen.Plant Material and Growth ConditionsArabidopsis (Arabidopsis thaliana) T-DNA insertional knockout lines for Tric1 (SALK_031707, SALK_112126, and At3g49560) and Tric2 (SALK_136525, SALK_149871, and At5g24650) were obtained from ABRC and sc ]]></description>
	<pubDate>Tue, 11 Aug 2020 18:32:14 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-6</guid>
</item>

<item>
	<title><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7"><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the]]></source>
	<description><![CDATA[On kit (Promega); 10 mL of radiolabeled protein was added to the reaction, and samples were resolved by SDS-PAGE, dried, and exposed to a phosphor-imaging screen.Plant Material and Growth ConditionsArabidopsis (Arabidopsis thaliana) T-DNA insertional knockout lines for Tric1 (SALK_031707, SALK_112126, and At3g49560) and Tric2 (SALK_136525, SALK_149871, and At5g24650) were obtained from ABRC and sc ]]></description>
	<pubDate>Tue, 11 Aug 2020 18:31:18 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=on-kit-promega-10-ml-of-radiolabeled-protein-was-added-to-the-7</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Tue, 11 Aug 2020 18:14:55 +0000</pubDate>
	<author>taxhill37</author>
	<category>News</category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-4</guid>
</item>

<item>
	<title><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></title>
	<link>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1</link>
	<source url="https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1"><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha]]></source>
	<description><![CDATA[Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w ]]></description>
	<pubDate>Thu, 06 Aug 2020 22:52:16 +0000</pubDate>
	<author>taxhill37</author>
	<category></category>
	<votes>1</votes>
	<guid>https://slavyanski.net/sb2020/story.php?title=flanked-by-gateway-recombination-cassettes-supplemental-table-s4-and-cloned-intomurcha-1</guid>
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