Webpolypeptide fusion partner, termed affinity tag, to facil-itate the purification of the target polypeptides are widely used. Many different proteins, domains, or peptides can be fused with the target protein. The advantages of using fusion proteins to facilitate purification and detection of recombinant proteins are well-recognized. Nevertheless, WebGenScript Anti-DYKDDDDK G1 Affinity Resin (Cat. No. L00432) is designed for the purification of DYKDDDDK-tagged protein from commonly used protein expression systems including bacteria, yeast and mammalian cells. The DYKDDDDK-tagged protein in the cell lysate can specifically bind to the anti-DYKDDDDK monoclonal antibodies …
Immunoprecipitation of FLAG Fusion Proteins Using Monoclonal …
WebApr 13, 2024 · The affinity-purified biotinylated RNA corresponding to NAD-capped RNA was eluted from streptavidin beads and visualized using IRDye® 800CW as in ( d ). Full … WebOct 30, 2001 · When covalently attached to a solid support, the anti-Flag M1 antibody can be used for the rapid purification of FLAG™ fusion proteins in a mild, calcium-dependent affinity chromatography procedure [1], [12], [27]. FLAG™ fusion proteins are typically purified to homogeneity in a single step, starting from a crude cell homogenate or ... shut d0wn all n0w n0w
Interactome study suggests multiple cellular functions of …
WebWe adapted a simple protocol for FLAG-based affinity purification of TET enzymes from Sf9 cells; the volumes below are for purification from a 500 mL culture. Resuspend the cell pellet in 10 mL of lysis buffer (50 m M HEPES, pH 7.5, 300 m M NaCl, 0.2% (v/v) NP-40) with cOmplete, EDTA-free Protease Inhibitor Cocktail (Roche, 1 tablet/10 mL) and ... WebAnti-DYKDDDDK tag Affinity Beads (Binds to FLAG ® tag sequence) (ab270704) is an affinity chromatography medium designed for easy, one-step purification or immunoprecipitation of DYKDDDDK (flag) at N-terminal, C-terminal and internal locations of a fusion protein. WebThe standard FLAG ® peptide (sequence: DYKDDDDK) is a small tag that can be incorporated with minimal risk of steric hindrance or negative impact on protein solubility. … shut d0wn all n0w f0r me