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Protein purification

  • Why Did My Nickel Agarose Beads Lose Their Color?

    Why Did My Nickel Agarose Beads Lose Their Color?

    Ni2+ ions give nickel agarose beads their characteristic blue color. This blue color can fade or disappear completely when loading his-tagged proteins onto the column....

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  • Nickel agarose bead turning brown thumbnail image

    Why Did My Nickel Agarose Beads Turn Black or Brown?

    Nickel agarose beads change from blue to a brown or black color when the nickel ions have been reduced from a Ni2+ to a Ni1+...

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  • Why are nickel agarose beads blue - thumbnail

    Why Are Nickel Agarose Beads Blue?

    The characteristic blue color of nickel agarose beads comes from the 2+ oxidation state of the nickel ions. Color is also a useful indicator for...

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  • IDA vs. Nickel Beads thumbnail and banner image

    What’s the Difference Between Nickel NTA and Nickel IDA Agarose Beads?

    While very similar overall, the fundamental difference between NTA and IDA is that NTA forms 4 bonds with a nickel ion whereas IDA makes 3...

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  • Nickel Agarose Bead Binding capacity article thumbnail and banner

    Understanding Binding Capacity for Nickel Agarose Beads

    The reported binding capacity of GoldBio’s nickel agarose beads ranges from 6 to 80 milligrams (mg) of his-tagged protein per milliliter (mL) of resin. The...

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  • Hydrophobic interaction chart - banner image

    An Overview of Hydrophobic Interaction Chromatography

    Have you ever felt as if all of your contributions in the lab go unseen and unappreciated? That if only someone would pay attention, they...

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  • What is a GST Pull-Down Assay? The Complete Overview with Protocols and Analyses Guides

    What is a GST Pull-Down Assay? The Complete Overview with Protocols and Analyses Guides

    GST pull-down assays are used to identify protein-protein interactions. A GST-tagged protein is immobilized on glutathione agarose beads and used to pull down interacting proteins...

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  • Glutathione columns - article thumbnail and banner

    How to Regenerate Glutathione Resin

    Glutathione agarose beads are cleaned and regenerated by alternating several column volumes of: 1) 0.1M Tris-HCl pH 8.5, 0.5M NaCl, and 2) 0.1M sodium acetate...

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  • insoluble protein  inclusion body - thumbnail

    Insoluble Protein Purification: How To Get Proteins Out of Inclusion Bodies?

    Proteins are extracted from inclusion bodies using solubilizing salts like guanidine and reducing agents like TCEP. The extracted proteins are then purified and refolded. Functional...

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  • Salting in and salting out article banner

    Understanding Salting In and Salting Out: Salt as a Protein Purification Tool

    Salting in is adding salt to a solution to enhance the solubility of a protein, whereas salting out is adding salt to precipitate a protein....

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  •  protein - solubility tags for protein purification

    GST Tag, MBP Tag, and SUMO Tag: 3 Solubility Tags for Protein Affinity Purification

    GST-, MBP-, and SUMO-tags are three affinity tags that help solubilize recombinant proteins. These solubility tags are complete protein domains, so they are much larger...

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  • GST-Tagged Protein Purification

    GST-Tagged Protein Purification

    There are a number of great methods in the researcher’s toolbox for protein purification. Along with the ever popular His-Tagged protein purification, there is also...

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