GTX109821 WB Image
GTX109821 WB Image
LYAG antibody [C2C3], C-term
GTX109821
Product group Antibodies
Overview
- SupplierGeneTex
- Product NameLYAG antibody [C2C3], C-term
- Delivery Days Customer9
- CertificationResearch Use Only
- Concentration1.01 mg/ml
- IsotypeIgG
- Scientific DescriptionThis gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompes disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq]
- Storage Instruction2°C to 8°C,-20°C
- UNSPSC12352203
References
- Efficient therapy for refractory Pompe disease by mannose 6-phosphate analogue grafting on acid alpha-glucosidase. Basile I et al., 2018 Jan 10, J Control ReleaseRead more