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Catalog Number | orb1959051 |
---|---|
Category | Small Molecules |
Description | SBDS Protein, Human, Recombinant (His) |
Purity | 98.00% |
MW | Approxiamtely 31 kDa |
Biological Activity | The mutation of Shwachman-Bodian-Diamond syndrome (SBDS) gene has been proposed to be a major causative reason for SDS. Shwachman-Diamond syndrome (SDS) is a rare pediatric disease characterized by various systemic disorders, including hematopoietic dysfunction. SBDS deficiency leads to telomere shortening, that SBDS is a telomere-protecting protein that participates in regulating telomerase recruitment. |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
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