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Molecular mass of solubilized CipA and CipB was determined by <t>SEC-MALS.</t> Light scattering (left axis) and molecular mass (right axis) are plotted by black dots and red dots in each panel. (A) CipA at pH 3.5. (B) CipA at pH 10.6. (C) CipB at pH 3.5. (D) CipB at pH 10.6.
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Molecular mass of solubilized CipA and CipB was determined by SEC-MALS. Light scattering (left axis) and molecular mass (right axis) are plotted by black dots and red dots in each panel. (A) CipA at pH 3.5. (B) CipA at pH 10.6. (C) CipB at pH 3.5. (D) CipB at pH 10.6.

Journal: bioRxiv

Article Title: Demixing of bacterial CipA and CipB proteins in mammalian cell cytosol provides an orthogonal self-assembly platform for producing isolable multi-phase intracellular crystals

doi: 10.64898/2026.05.10.724141

Figure Lengend Snippet: Molecular mass of solubilized CipA and CipB was determined by SEC-MALS. Light scattering (left axis) and molecular mass (right axis) are plotted by black dots and red dots in each panel. (A) CipA at pH 3.5. (B) CipA at pH 10.6. (C) CipB at pH 3.5. (D) CipB at pH 10.6.

Article Snippet: SEC–MALS was performed using an Agilent 1290 UPLC system interfaced with a Wyatt DAWN MALS detector and an Optilab refractive index detector.

Techniques:

Journal: bioRxiv

Article Title: Demixing of bacterial CipA and CipB proteins in mammalian cell cytosol provides an orthogonal self-assembly platform for producing isolable multi-phase intracellular crystals

doi: 10.64898/2026.05.10.724141

Figure Lengend Snippet:

Article Snippet: SEC–MALS was performed using an Agilent 1290 UPLC system interfaced with a Wyatt DAWN MALS detector and an Optilab refractive index detector.

Techniques: Sequencing