Enzyme

Initiates the repair of damaged proteins by catalyzing methyl esterification of L-isoaspartyl and D-aspartyl residues produced by spontaneous isomerization and

Carbonic Anhydrase 2 Protein, Human, Recombinant (His) is expressed in E.

Protein-Tyrosine Phosphatase 1C (PTP1C) belongs to the protein-tyrosine phosphatase family.which is known to be signaling molecules that regulate a variety of

SVMP Protein, Bothrops atrox, Recombinant (His & Myc) is expressed in E.

Removes the formyl group from the N-terminal Met of newly synthesized proteins.

Carbonic Anhydrase 4 Protein, Human, Recombinant (His) is expressed in CHO mammalian cells with His tag.

SMYD3 Protein, Human, Recombinant (His & Myc) is expressed in E. coli.

NIMA (never in mitosis gene a)-related kinase 7, NEK7 belongs to the NIMA subfamily, NEK Ser/Thr protein kinase family, protein kinase superfamily.

Converts O-phosphoseryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis.

CKM, also known as CK-MM, is mainly expressed in skeletal muscle.

Catalyzes the removal of sialic acid (N-acetylneuraminic acid) moieties from glycoproteins, oligosaccharides and gangliosides.

Peptidyl-prolyl cis-trans isomerase A is a cytoplasm protein which belongs to the cyclophilin-type PPIase family and PPIase A subfamily.

Catalyzes oxygen-dependent 5-hydroxyuridine (ho5U) modification at position 34 in tRNAs.

Butyrylcholinesterase Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag.

L-saccharopine oxidase Protein, S.

Hydrolyzes galactooligomers with a degree of polymerization higher than 3.

Plasma membrane-anchored serine protease that participates in proteolytic cascades of relevance for the normal physiologic function of the prostate.

HNMT (Histamine N-methyltransferase) is a Protein Coding gene.

EIF4A2 Protein, Human, Recombinant (GST) is expressed in E.

Sialic acid aldolase - Aqueous solution is an enzyme preparation used extensively in biochemical and biotechnological applications. It is derived from microbial sources, where it is expressed and purified to high levels for research purposes. Sialic acid aldolase acts by catalyzing the reversible aldol reaction between N-acetylneuraminic acid (sialic acid) and pyruvate, facilitating the cleavage or synthesis of sialic acid. This enzyme is instrumental in the study of sialic acid metabolism and is employed in various applications, including the synthesis of sialic acid derivatives and the structural analysis of complex carbohydrates. Its ability to catalyze the formation and breakdown of sialic acid makes it a valuable tool in the investigation of glycoproteins and glycolipids, which are critical components of cellular communication and pathogen-host interactions. Additionally, the enzyme's application extends to the development of novel therapeutic agents and diagnostic techniques, highlighting its significance in advancing scientific understanding and innovation.