Methods for isolating proteins from a honey sample are provided. The methods include contacting the honey sample with a substrate functionalized with one or more reactive dyes and recovering proteins associated with the substrate. Methods for detecting proteins in a honey sample and assessing the risk of colony collapse disorder are also provided.

Chromatography resins having mixed mode ligands and methods of using such resins are provided.

The invention relates to an affinity resin functionalized with small molecule inhibitors of glycoside-cleaving enzymes, e.g., -galactosidase A (-Gal A), glucocerebrosidase (GCB), -galactosidase, and acid alpha-glucosidase (GAA), and a method for purifying glycoside-cleaving enzymes produced in a cell line using the small molecule inhibitor-functionalized affinity resin.

There is provided a deodorizing material having particularly high deodorization capabilities for ammonia, acetaldehyde, and toluene. The deodorizing material of the present invention comprises fibrous activated carbon; and (A) an aromatic amine and a sulfate of the aromatic amine or (B) an aromatic amine, a sulfate of the aromatic amine, and sulfuric acid, supported on the fibrous activated carbon, wherein a total substance amount of the aromatic amine and the sulfate of the aromatic amine supported per gram of the fibrous activated carbon is 0.85 to 1.35 mmol, and a ratio of the total substance amount (mmol) of the aromatic amine and the sulfate of the aromatic amine supported per gram of the fibrous activated carbon relative to a total substance amount (mmol) of the sulfate of the aromatic amine and the sulfuric acid supported per gram of the fibrous activated carbon ([total substance amount of the aromatic amine and the sulfate of the aromatic amine][total substance amount of the sulfate of the aromatic amine and the sulfuric acid]) is 5.0 to 7.5.

Chromatography resins having anionic exchange-hydrophobic mixed mode ligands and methods of using such resins are provided.

This invention relates to a hybrid ligand, a hybrid biomimetic chromedia and a preparing method and a use thereof, wherein the hybrid biomimetic chromedia takes hydrophilic porous microsphere as a substrate in chromatography, activated with allyl bromide and undergoing bromo-alcoholization with N-bromosuccinimide, then coupled with the hybrid ligands. The sequence of the hybrid ligand is phenylalanine-tyrosine-glutamine-5-aminobenzimidazole. The hybrid biomimetic chromedia has both of the two functional groups of phenylalanine-tyrosine-glutamine tripeptide and aminobenzimidazole, while maintaining the high antibody selectivity of polypeptide ligand, hydrophobic electric charge inductive ligand is introduced to achieve more moderate elution requirement, realizing effective antibody separation.

Chromatography resins having anionic exchange-hydrophobic mixed mode ligands, that are useful for purifying target biomolecules using anionic exchange (i.e., where the ligand is positively charged) and hydrophobic mixed mode chromatography. The chromatography resins allow for efficient purification of target biomolecules (e.g., recombinant proteins, antibodies, antibody-drug conjugates, or antibody derivatives including, but not limited to, antibody fragments and antibody fusions) from a sample, and have been found to be useful in purifying monomeric target biomolecules from aggregate target biomolecules. In an embodiment, the chromatography resins are useful for separating antibodies from one or more components (e.g., contaminants) in the sample.

The invention discloses a separation matrix which comprises a plurality of separation ligands, defined by the formula R.sub.1-L.sub.1-N(R.sub.3)-L.sub.2-R, immobilized on a support, wherein R.sub.1 is a five- or six-membered, substituted or non-substituted ring structure or a hydroxyethyl or hydroxypropyl group; L.sub.1 is either a methylene group or a covalent bond; R.sub.2 is a five-or six-membered, substituted or non-substituted ring structure; L.sub.2 is either a methylene group or a covalent bond; R.sub.3 is a methyl group; and wherein if R.sub.1 is a hydroxyethyl group and L.sub.1 is a covalent bond, R.sub.2 is a substituted aromatic ring structure or a substituted or non-substituted aliphatic ring structure.

A method for solid-phase extraction is disclosed. The method includes fabricating a solid-phase extraction medium by incorporating a plurality of modified mesoporous silica particles within pores of a cotton fabric matrix, putting the solid-phase extraction medium in contact with a fluid containing metal ions including one of immersing the solid-phase extraction medium in the fluid containing metal ions or passing the fluid containing metal ions through the solid-phase extraction medium by continuously circulating the fluid through the solid-phase extraction medium, and extracting the metal ions from the fluid by adsorbing the metal ions onto the solid-phase extraction medium responsive to a contact between the solid-phase extraction medium and the fluid containing metal ions.

The present invention relates to a chromatography ligand defined by the following formula R.sub.1R.sub.2N(R.sub.3)R.sub.4R.sub.5 wherein R.sub.1 is a substituted or non-substituted phenyl group; R.sub.2 is a hydrocarbon chain comprising 0-4 carbon atoms; R.sub.3 is a hydrocarbon chain comprising 1-3 carbon atoms; R.sub.4 is a hydrocarbon chain comprising 1-5 carbon atoms; and R.sub.5 is OH or H. The invention also comprises a separation matrix, comprising the described ligands coupled to a porous support, such as particles or a membrane. The ligand and matrix according to the invention is useful for purification of biomolecules or organic compounds, such as proteins, polypeptides, DNA etc. An advantageous use according to the invention is the purification of antibodies.