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| Product Name | Glucosylsphingosine Analysis |
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| 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. |
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| Size | n/a |
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| Gene, Accession, CAS # | n/a |
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| Order / More Info | Glucosylsphingosine Analysis from CREATIVE PROTEOMICS |
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| Product Specific References | n/a |
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