Primärantikörper geliefert von Boster Bio
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Die lysosomale Alpha-Glucosidase ist ein Enzym, das beim Menschen durch das GAA-Gen kodiert wird. Dieses Gen kodiert die lysosomale Alpha-Glucosidase, die für den Abbau von Glykogen zu Glukose in Lysosomen unerlässlich ist. Das kodierte Präproprotein wird proteolytisch prozessiert, um mehrere Zwischenformen und die reife Form des Enzyms zu erzeugen. Defekte in diesem Gen sind die Ursache für die Glykogenspeicherkrankheit II, auch bekannt als Morbus Pompe, eine autosomal-rezessive Erkrankung mit einem breiten klinischen Spektrum. Alternatives Spleißen führt zu mehreren Transkriptvarianten.
Fully tested in-house by ABMIUM. Highest confidence. Non-conformities fully supported under the ABMIUM Product Promise.
Quality verified. Independent collaborator or expected-performance data available. Product meets ABMIUM quality standards.
Expected to work based on structural and biochemical data. Not yet directly tested by ABMIUM or a collaborator. No non-conformity support for this combination.
Not recommended for this application or species/sample combination. This may indicate either evidence of unsuitability or that the combination has not been tested and therefore cannot currently be recommended.
Evidence status by application and model.
| Arten | WB | IHC | IHC-P | IHC-F | IF/ICC | Durchflusszytometrie | ELISA | IP |
|---|---|---|---|---|---|---|---|---|
| Human |
This product is manufactured by Boster Bio and sold through ABMIUM without relabelling.
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Yes. Send your target, sample, application and experimental conditions through ABMIUM MATCH or technical support.
Unless the listing expressly states otherwise, ABMIUM products are supplied for research use only and are not for diagnostic or therapeutic use.