TMPY-00518
SBDS Protein, Human, Recombinant (His)
TargetMol
DESCRIPTION
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.
DETAILS
- Purity: 98%
- Category: Compound
- Molecular Weight: Approxiamtely 31 kDa
Lead Time: 4 - 5 weeks
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