Article No
GTX01987
Application | IP, WB |
Article No | GTX01987 |
Country Availability | SE, FI, DK, NO, IS, EE, LV, LT |
Clone | 1 |
Clone Type | monoclonal |
Conjugation | Unconjugated |
Description | Galactosidase alpha antibody [001] |
Supplier | GeneTex |
Entrez Gene ID | 2717 |
Gene Symbol | GLA |
Immunogen | Recombinant Human alpha-Galactosidase A / GLA protein |
Isotype | IgG |
Notes | This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq, Jul 2008] |
Product Type | Antibodies Primary |
Protocol | WB: 1:1000-1:5000. IP: 4-6 µl/mg of lysate. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications. |
Purification | Protein A Purified |
Size | 100µl |
Source / Host | rabbit |
Species Reactivity | human |
Storage | 4°C, -80°C |
UniProt Number | P06280 |
Product Page Updated | 2024-01-03T10:31:47.950Z |