gel filtration chromatography Search Results


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gel filtration chromatography  (BIOSAXS GmbH)
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BIOSAXS GmbH gel filtration chromatography
(A) Gel <t>filtration</t> <t>chromatography</t> profile of UbV3 V10G construct and UbV3. With the aid of standards, UbV3 V10G was clearly identified as monomer instead of being a dimer like UbV3. (B) Cartoon representation of the UbV3 dimer. (C) Backbone hydrogen bond network near strand β1 that holds the UbV monomer together through strand exchange. (D) β1-β2 loop structure. (E) Substitutions in UbV3 compared to wild type Ub. UbV3 chains are colored as cyan and green, and ubiquitin (PDB ID: 1UBQ) is colored as salmon. Substitutions around strand β1 are described on top panel, and substitutions around β1-β2 loop are described on bottom panel. (F) Hydrophobic sidechains near I36 patch interact with β1-β2 loop region.
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gel filtration chromatography  (IBA GmbH)
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IBA GmbH gel filtration chromatography
(A) Gel <t>filtration</t> <t>chromatography</t> profile of UbV3 V10G construct and UbV3. With the aid of standards, UbV3 V10G was clearly identified as monomer instead of being a dimer like UbV3. (B) Cartoon representation of the UbV3 dimer. (C) Backbone hydrogen bond network near strand β1 that holds the UbV monomer together through strand exchange. (D) β1-β2 loop structure. (E) Substitutions in UbV3 compared to wild type Ub. UbV3 chains are colored as cyan and green, and ubiquitin (PDB ID: 1UBQ) is colored as salmon. Substitutions around strand β1 are described on top panel, and substitutions around β1-β2 loop are described on bottom panel. (F) Hydrophobic sidechains near I36 patch interact with β1-β2 loop region.
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gel filtration column chromatography  (GL Sciences)
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GL Sciences gel filtration column chromatography
(A) Gel <t>filtration</t> <t>chromatography</t> profile of UbV3 V10G construct and UbV3. With the aid of standards, UbV3 V10G was clearly identified as monomer instead of being a dimer like UbV3. (B) Cartoon representation of the UbV3 dimer. (C) Backbone hydrogen bond network near strand β1 that holds the UbV monomer together through strand exchange. (D) β1-β2 loop structure. (E) Substitutions in UbV3 compared to wild type Ub. UbV3 chains are colored as cyan and green, and ubiquitin (PDB ID: 1UBQ) is colored as salmon. Substitutions around strand β1 are described on top panel, and substitutions around β1-β2 loop are described on bottom panel. (F) Hydrophobic sidechains near I36 patch interact with β1-β2 loop region.
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Image Search Results


(A) Gel filtration chromatography profile of UbV3 V10G construct and UbV3. With the aid of standards, UbV3 V10G was clearly identified as monomer instead of being a dimer like UbV3. (B) Cartoon representation of the UbV3 dimer. (C) Backbone hydrogen bond network near strand β1 that holds the UbV monomer together through strand exchange. (D) β1-β2 loop structure. (E) Substitutions in UbV3 compared to wild type Ub. UbV3 chains are colored as cyan and green, and ubiquitin (PDB ID: 1UBQ) is colored as salmon. Substitutions around strand β1 are described on top panel, and substitutions around β1-β2 loop are described on bottom panel. (F) Hydrophobic sidechains near I36 patch interact with β1-β2 loop region.

Journal: PLOS Pathogens

Article Title: Suppressing Tymovirus replication in plants using a variant of ubiquitin

doi: 10.1371/journal.ppat.1012899

Figure Lengend Snippet: (A) Gel filtration chromatography profile of UbV3 V10G construct and UbV3. With the aid of standards, UbV3 V10G was clearly identified as monomer instead of being a dimer like UbV3. (B) Cartoon representation of the UbV3 dimer. (C) Backbone hydrogen bond network near strand β1 that holds the UbV monomer together through strand exchange. (D) β1-β2 loop structure. (E) Substitutions in UbV3 compared to wild type Ub. UbV3 chains are colored as cyan and green, and ubiquitin (PDB ID: 1UBQ) is colored as salmon. Substitutions around strand β1 are described on top panel, and substitutions around β1-β2 loop are described on bottom panel. (F) Hydrophobic sidechains near I36 patch interact with β1-β2 loop region.

Article Snippet: Purified UbV3 dimer from gel filtration chromatography was sent to B21 BioSAXS beamline at Diamond Light Source (Didcot, Oxfordshire, UK).

Techniques: Filtration, Chromatography, Construct, Ubiquitin Proteomics