Gxene Biotech has been working on recombinant protein expression and antibody development, and has maintained high-quality requirement to produce clean and reproducible results for purification. You have access to customized protein purification services, including tag/tag-free recombinant proteins, purification and separation of natural proteins. Our laboratory has more than a dozen GE purification resins that enable simultaneous large-scale scanning protein purification and separation, saving you time and money.
Gxene Biotech can provide natural and recombinant proteins purification services:
Natural Protein Purification Service:
Project Name |
Protocol |
Separation and purification of natural macromolecular proteins |
* Separation and purification proteins using molecular sieves of appropriate pore size, combined with anion and cation adsorption columns and HLPC, identify and collect corresponding elution peaks. |
Separation and purification of natural small molecular proteins |
* Multi-layer separation and filtration combined with molecular sieve to remove macromolecular impurities, combined with macroporous resin or reverse resin to purify small molecular proteins, purified by HPLC and MS. |
Separation and purification of mixed unknown protein samples |
* Separation and purification were carried out by Gxene Biotech, and identified by mass spectrometry, activity identification, etc. |
Recombinant Protein Purification Services:
Project Name |
Protocol |
Deproteinization, separation and purification of recombinant proteins |
* Commercially purified resin, such as Ni column, GST-Beads, etc., and purified with 6xHis, GST, SUMO, MBP to obtain a fusion protein with a purity > 90%. |
Tag free recombinant protein purification |
* Antibody affinity purification; also can be selected similar to the natural protein purification method, depending on the project. |
Inclusion body denaturation and renaturation purification |
* According to the different properties of the protein, urea, guanidine hydrochloride, detergent, extreme pH, etc. can be selected to ensure the monomeric state's maximum denaturation. |