Thermo Fisher Scientific AGA Polyclonal Antibody
Rabbit polyclonal antibody against human AGA protein for WB, IHC, and ICC applications. Affinity-purified with >95% purity. Supplied as liquid, unconjugated form at 1 mg/mL concentration. Stored in PBS with glycerol and sodium azide for research use only.
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Thermo Fisher Scientific AGA Polyclonal Antibody
Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:2,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Immunocytochemistry (ICC/IF) | 1:50–1:200 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant full-length Human AGA (UniProt ID: P20933-1, 1–346 aa) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2720638 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum using an epitope-specific immunogen. Purity is >95% as confirmed by SDS-PAGE.
Target Information
Aspartylglucosaminidase (AGA) is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines during lysosomal glycoprotein degradation. Deficiency in AGA causes the lysosomal storage disease aspartylglycosaminuria. Alternatively spliced transcript variants have been identified.
For Research Use Only. Not for use in diagnostic procedures or resale without authorization.
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