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LYAG KO Cell Line
SPL-01447
| Size | Price |
| 1 Unit | Online Inquiry |
| Description |
|---|
| LYAG KO |
| Target Information | |
|---|---|
| Target Name | GAA |
| Gene Abbr. | GAA |
| Gene ID | 2548 |
| Full Name | alpha glucosidase |
| Alias | LYAG |
| Species | Human |
| Genomic Locus | chr17:80105855 |
| Introduction | 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]. |
| Product Details | |
|---|---|
| Cell Line Model | HAP1 |
| Genotype | LYAG KO |
| Description | LYAG KO |
| Parental Cell Line | C631 |
| Handling Specifications | |
|---|---|
| Culture Medium | IMDM + 10% FCS |
| Disclaimer | This product is classified under IATA regulations as a GMMO (genetically modified micro-organism) and will ship as UN3245. If applicable, ensure facility meets all requirements per local and country regulations. |
For research use only. Not intended for any clinical use. No products from CD BioSciences may be resold, modified for resale or used to manufacture commercial products without prior written approval from CD BioSciences.