| 產(chǎn)品詳情 |
| Edit |   |
| Product Name | Glucosylsphingosine Analysis |
| Description | Gaucher disease is an autosomal recessive lysosomal storage disease caused by a deficiency of glucosylceramidase (β-glucosidase), which results in the abnormal accumulation of glucosylceramide (GlcCer) in tissues. The accumulation of glucosylsphingosine (GlcSph), a derivative of GlcCer devoid of fatty acids, has been demonstrated in the affected tissues of patients with Gaucher disease. |
| Size | n/a |
| Concentration | n/a |
| Applications | n/a |
| Other Names | n/a |
| Gene, Accession, CAS # | n/a |
| Catalog # | n/a |
| Price | |
| Order / More Info | Glucosylsphingosine Analysis from CREATIVE PROTEOMICS |
| Product Specific References | n/a |
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