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Species | Human |
Cat.No | ABC-KC0726 |
Product Category | Transfected Stable Cell Lines |
Size/Quantity | 100ug |
Shipping Info | Ice Pack |
Growth Conditions | 37 ℃, 5% CO2 |
Storage | Store GAA KO Cell Lysate At -20℃. Please Avoid Repeated Freeze-Thaw Cycles. |
Product Type | CRISPR Knockout Cell Lysate |
Host Cell | HEK293T |
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe’s disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
For research use only