size exclusion chromatography sec buffer Search Results


90
Anatrace size exclusion chromatography purification buffer
Size Exclusion Chromatography Purification Buffer, supplied by Anatrace, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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size exclusion chromatography purification buffer - by Bioz Stars, 2026-04
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90
Fisher Scientific size-exclusion chromatography-multi-angle light scattering buffer
Pot1-DBD forms primarily a 1:1 complex at low concentrations and can form a larger complex at high concentrations in the presence of 12mer, but not 15mer. Amino acid mutation or base substitution can switch between these two binding modes. ( A ) RI traces (lines) and molar masses calculated by MALS (markers) of 34 μM Pot1-DBD+15mer and 34 μM Pot1-DBD+12mer complexes in <t>20</t> <t>mM</t> Tris–HCl pH 8.0, 50 mM NaCl. ( B ) Increasing the concentration of NaCl to 400 mM causes Pot1-DBD+12mer to elute earlier than Pot1-DBD+15mer and with a variable but larger average molar mass. Protein and DNA are both at 34 μM. ( C ) Increasing the concentration of Pot1-DBD to 170 μM and increasing the molar ratio to 2:1, Pot1-DBD:oligonucleotide pushes the 12mer-binding mode toward the 2:1 complex. This 12mer-binding mode can be forced to form a 1:1 complex upon 12mer_T9A substitution. Conversely, Pot1-DBD_Y224A mutation or 15mer_G13C substitution can switch the 15mer-binding mode to the 12mer-binding mode. All complexes were injected at 170 μM protein + 85 μM DNA.
Size Exclusion Chromatography Multi Angle Light Scattering Buffer, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/size-exclusion chromatography-multi-angle light scattering buffer/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
size-exclusion chromatography-multi-angle light scattering buffer - by Bioz Stars, 2026-04
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90
CANTEST Ltd buffer for size exclusion chromatography
Pot1-DBD forms primarily a 1:1 complex at low concentrations and can form a larger complex at high concentrations in the presence of 12mer, but not 15mer. Amino acid mutation or base substitution can switch between these two binding modes. ( A ) RI traces (lines) and molar masses calculated by MALS (markers) of 34 μM Pot1-DBD+15mer and 34 μM Pot1-DBD+12mer complexes in <t>20</t> <t>mM</t> Tris–HCl pH 8.0, 50 mM NaCl. ( B ) Increasing the concentration of NaCl to 400 mM causes Pot1-DBD+12mer to elute earlier than Pot1-DBD+15mer and with a variable but larger average molar mass. Protein and DNA are both at 34 μM. ( C ) Increasing the concentration of Pot1-DBD to 170 μM and increasing the molar ratio to 2:1, Pot1-DBD:oligonucleotide pushes the 12mer-binding mode toward the 2:1 complex. This 12mer-binding mode can be forced to form a 1:1 complex upon 12mer_T9A substitution. Conversely, Pot1-DBD_Y224A mutation or 15mer_G13C substitution can switch the 15mer-binding mode to the 12mer-binding mode. All complexes were injected at 170 μM protein + 85 μM DNA.
Buffer For Size Exclusion Chromatography, supplied by CANTEST Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/buffer for size exclusion chromatography/product/CANTEST Ltd
Average 90 stars, based on 1 article reviews
buffer for size exclusion chromatography - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

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Pot1-DBD forms primarily a 1:1 complex at low concentrations and can form a larger complex at high concentrations in the presence of 12mer, but not 15mer. Amino acid mutation or base substitution can switch between these two binding modes. ( A ) RI traces (lines) and molar masses calculated by MALS (markers) of 34 μM Pot1-DBD+15mer and 34 μM Pot1-DBD+12mer complexes in 20 mM Tris–HCl pH 8.0, 50 mM NaCl. ( B ) Increasing the concentration of NaCl to 400 mM causes Pot1-DBD+12mer to elute earlier than Pot1-DBD+15mer and with a variable but larger average molar mass. Protein and DNA are both at 34 μM. ( C ) Increasing the concentration of Pot1-DBD to 170 μM and increasing the molar ratio to 2:1, Pot1-DBD:oligonucleotide pushes the 12mer-binding mode toward the 2:1 complex. This 12mer-binding mode can be forced to form a 1:1 complex upon 12mer_T9A substitution. Conversely, Pot1-DBD_Y224A mutation or 15mer_G13C substitution can switch the 15mer-binding mode to the 12mer-binding mode. All complexes were injected at 170 μM protein + 85 μM DNA.

Journal: Nucleic Acids Research

Article Title: The telomeric protein Pot1 from Schizosaccharomyces pombe binds ssDNA in two modes with differing 3′ end availability

doi: 10.1093/nar/gku680

Figure Lengend Snippet: Pot1-DBD forms primarily a 1:1 complex at low concentrations and can form a larger complex at high concentrations in the presence of 12mer, but not 15mer. Amino acid mutation or base substitution can switch between these two binding modes. ( A ) RI traces (lines) and molar masses calculated by MALS (markers) of 34 μM Pot1-DBD+15mer and 34 μM Pot1-DBD+12mer complexes in 20 mM Tris–HCl pH 8.0, 50 mM NaCl. ( B ) Increasing the concentration of NaCl to 400 mM causes Pot1-DBD+12mer to elute earlier than Pot1-DBD+15mer and with a variable but larger average molar mass. Protein and DNA are both at 34 μM. ( C ) Increasing the concentration of Pot1-DBD to 170 μM and increasing the molar ratio to 2:1, Pot1-DBD:oligonucleotide pushes the 12mer-binding mode toward the 2:1 complex. This 12mer-binding mode can be forced to form a 1:1 complex upon 12mer_T9A substitution. Conversely, Pot1-DBD_Y224A mutation or 15mer_G13C substitution can switch the 15mer-binding mode to the 12mer-binding mode. All complexes were injected at 170 μM protein + 85 μM DNA.

Article Snippet: Pot1-DBD and the Y224A mutant were buffer exchanged and concentrated in size-exclusion chromatography-multi-angle light scattering (SEC-MALS) buffer (20 mM Tris–HCl pH 8.0 and 50/400 mM NaCl) using 10 000 MWCO Vivaspin Turbo concentrators pre-rinsed with water (Fisher Scientific).

Techniques: Mutagenesis, Binding Assay, Concentration Assay, Injection