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The expression region of this recombinant Human FUCA2 covers amino acids 29-465. The theoretical molecular weight of the FUCA2 protein is 77.7 kDa. This protein is generated in a e.coli-based system. The N-terminal GST tag was fused into the coding gene segment of FUCA2, making it easier to detect and purify the FUCA2 recombinant protein in the later stages of expression and purification.Human plasma alpha-L-fucosidase, encoded by the FUCA2 gene, is an enzyme involved in the hydrolysis of alpha-L-fucosidic linkages in various glycoconjugates. This lysosomal enzyme plays a crucial role in the degradation of complex carbohydrates, including glycoproteins and glycolipids containing terminal fucose residues, contributing to cellular homeostasis. Deficiencies in human FUCA2 are associated with fucosidosis, a lysosomal storage disorder characterized by the accumulation of fucose-containing substances. The study of FUCA2 contributes to understanding lysosomal function, glycoprotein metabolism, and the pathological mechanisms underlying fucosidosis, providing insights into potential therapeutic strategies for lysosomal storage disorders.
The expression region of this recombinant Human FUCA2 covers amino acids 29-465. The theoretical molecular weight of the FUCA2 protein is 77.7 kDa. This protein is generated in a e.coli-based system. The N-terminal GST tag was fused into the coding gene segment of FUCA2, making it easier to detect and purify the FUCA2 recombinant protein in the later stages of expression and purification.Human plasma alpha-L-fucosidase, encoded by the FUCA2 gene, is an enzyme involved in the hydrolysis of alpha-L-fucosidic linkages in various glycoconjugates. This lysosomal enzyme plays a crucial role in the degradation of complex carbohydrates, including glycoproteins and glycolipids containing terminal fucose residues, contributing to cellular homeostasis. Deficiencies in human FUCA2 are associated with fucosidosis, a lysosomal storage disorder characterized by the accumulation of fucose-containing substances. The study of FUCA2 contributes to understanding lysosomal function, glycoprotein metabolism, and the pathological mechanisms underlying fucosidosis, providing insights into potential therapeutic strategies for lysosomal storage disorders.
| Cat.No | ACP02643 | Target Name | FUCA2 |
|---|---|---|---|
| Form | Liquid or Lyophilized powder | Expression System | E.coli |
| Expression Range | 29-465aa | Mol Weight | 77.7 kDa |
| Protein Length | Partial | Purity | Greater than 85% as determined by SDS-PAGE. |
| Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q9BTY2 |
|---|
Uniprot Id
Q9BTY2
Target Species
Human
Target Name
FUCA2
Target Full Name
Plasma alpha-L-fucosidase
Target Function
Alpha-L-fucosidase is responsible for hydrolyzing the alpha-1,6-linked fucose joined to the reducing-end N-acetylglucosamine of the carbohydrate moieties of glycoproteins.
Target Subcellular Location
Secreted.
Target Protein Families
Glycosyl hydrolase 29 family
Target Research Area
Metabolism
Target Synonyms
Alpha L fucosidase 2; Alpha L fucosidase fucohydrolase 2; Alpha-L-fucosidase 2; Alpha-L-fucoside fucohydrolase 2; dJ20N2.5; FUCA 2; FUCA2; FUCO2; FUCO2_HUMAN; Fucosidase alpha L 2 plasma; Fucosidase; alpha-L; plasma; MGC1314; Plasma alpha L fucosidase; Plasma alpha-L-fucosidase; RP1 20N2.5
Target Background
This gene encodes a plasma alpha-L-fucosidase, which represents 10-20% of the total cellular fucosidase activity. The protein is a member of the glycosyl hydrolase 29 family, and catalyzes the hydrolysis of the alpha-1, 6-linked fucose joined to the reducing-end N-acetylglucosamine of the carbohydrate moieties of glycoproteins. This enzyme is essential for Helicobacter pylori adhesion to human gastric cancer cells.
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