<p>CotH-His was bound to a Ni-NTA column and the flowthrough (FT<sub>CotH</sub>) and washes (W1-W3, here only W3 is shown) were collected. Untagged CotE was then added, and flow through (FT<sub>CotE</sub>), washed (W1—W8, here only W8 is shown), and eluted (E1—E4) proteins collected as described in Materials and Methods. Proteins were fractionated on 12.5% polyacrylamide gels, electrotransferred to membranes, and reacted with anti-CotH (A), anti-CotE (B) antibodies. The same experiment was also performed without CotH-His (C).</p
Most mechanisms of cell development, physiology, and signal transduction are controlled by protein-p...
<p>(A) Co-immunoprecipitation pulldown assay (co-IP) with heterologously purified BEAF32 and Chromat...
<p>A. Schematic showing features of procyclic cell lines generated. B–D. Immunoprecipitation (IP) wa...
<p>(A) Western blot of proteins extracted from the forespore compartment of sporulating cells of a w...
<p>Proteins extracted from mature spores of a wild type strain or from isogenic strains over-produci...
<p>Western blot with anti-CotG (A) and anti-CotB (B) antibodies of proteins extracted from mature sp...
<p>Strains bearing versions of CotE lacking nine (A) or six (B) C-terminal amino acids were modified...
<p>(A) The amino acid sequences of the C termini of CotE and various mutant versions. To the left of...
<p>A) Pull-Down assay. The rEhCFIm25 immobilized on Ni<sup>2+</sup>-NTA column was incubated with NE...
<p>Proteins extracted from sporulating cells (forespores and mother cells) at various times during s...
<p>Co-immunoprecipitation was performed using the lysates of CSIAN cells, transiently expressing fla...
Coimmunoprecipitation is one of the most useful techniques for revealing protein-protein interaction...
<p>ELISA based protein-protein interaction study of PfMLH with PfUDN, PfUDC1, and PfUDC2. The protei...
<p>Although an extremely low amount of OsCYN proteins was detected in the input samples, an identica...
<p>Proteins for western blot analysis were extracted from: (A) mature spores of a wild type strain (...
Most mechanisms of cell development, physiology, and signal transduction are controlled by protein-p...
<p>(A) Co-immunoprecipitation pulldown assay (co-IP) with heterologously purified BEAF32 and Chromat...
<p>A. Schematic showing features of procyclic cell lines generated. B–D. Immunoprecipitation (IP) wa...
<p>(A) Western blot of proteins extracted from the forespore compartment of sporulating cells of a w...
<p>Proteins extracted from mature spores of a wild type strain or from isogenic strains over-produci...
<p>Western blot with anti-CotG (A) and anti-CotB (B) antibodies of proteins extracted from mature sp...
<p>Strains bearing versions of CotE lacking nine (A) or six (B) C-terminal amino acids were modified...
<p>(A) The amino acid sequences of the C termini of CotE and various mutant versions. To the left of...
<p>A) Pull-Down assay. The rEhCFIm25 immobilized on Ni<sup>2+</sup>-NTA column was incubated with NE...
<p>Proteins extracted from sporulating cells (forespores and mother cells) at various times during s...
<p>Co-immunoprecipitation was performed using the lysates of CSIAN cells, transiently expressing fla...
Coimmunoprecipitation is one of the most useful techniques for revealing protein-protein interaction...
<p>ELISA based protein-protein interaction study of PfMLH with PfUDN, PfUDC1, and PfUDC2. The protei...
<p>Although an extremely low amount of OsCYN proteins was detected in the input samples, an identica...
<p>Proteins for western blot analysis were extracted from: (A) mature spores of a wild type strain (...
Most mechanisms of cell development, physiology, and signal transduction are controlled by protein-p...
<p>(A) Co-immunoprecipitation pulldown assay (co-IP) with heterologously purified BEAF32 and Chromat...
<p>A. Schematic showing features of procyclic cell lines generated. B–D. Immunoprecipitation (IP) wa...