FUCA1 Polyclonal Antibody

Background:
The protein encoded by this gene is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. Mutations in this gene are associated with fucosidosis (FUCA1D), which is an autosomal recessive lysosomal storage disease. A pseudogene of this locus is present on chr 2.

Research Area: Metabolism, Signal Transduction

Synonyms:
Alpha L fucosidase I, Alpha L fucoside fucohydrolase, Alpha-L-fucosidase 1, Alpha-L-fucosidase I, Alpha-L-fucoside fucohydrolase 1, FUCA, FUCA1, FUCO, fucosidase, alpha-L, tissue, fucosidase, alpha-L- 1, tissue, Tissue alpha L fucosidase, Tissue alpha-L-fucosidase

Immunogen: Recombinant protein of human FUCA1

Swissprot: P04066
Gene Accession: BC017338

Calculated MW: 54 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.7 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:50-1:200

Storage:
Store at -20°C. Avoid freeze / thaw cycles.