Thermo Fisher Scientific alpha Galactosidase Recombinant Rabbit Monoclonal Antibody (30H11)
Human alpha-Galactosidase를 인식하는 Recombinant Rabbit Monoclonal Antibody입니다. IHC, Flow Cytometry, ELISA 등 다양한 응용에 적합합니다. HEK293 세포에서 발현되며, 고순도 Affinity chromatography로 정제되었습니다. 연구용으로만 사용 가능합니다.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Flow Cytometry (Flow) | 1:50–1:200 |
| ELISA | Assay-dependent |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | 30H11 |
| Immunogen | A synthesized peptide derived from Human GLA |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1.23 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C or -80°C if preferred |
| Shipping Conditions | Wet ice |
| RRID | AB_3092551 |
Target Information
This gene encodes a homodimeric glycoprotein that hydrolyzes the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. The enzyme predominantly hydrolyzes ceramide trihexoside and catalyzes the hydrolysis of melibiose into galactose and glucose. Mutations in this gene can affect the synthesis, processing, and stability of the enzyme, leading to Fabry disease — a rare lysosomal storage disorder caused by failure to catabolize alpha-D-galactosyl glycolipid moieties.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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