IDS 抗体
(Iduronate 2-Sulfatase (IDS))
Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence similarity with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Oct 2009].
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Latest Publications for our IDS 抗体
: "FGF signaling deregulation is associated with early developmental skeletal defects in animal models for mucopolysaccharidosis type II (MPSII)." in: Human molecular genetics, Vol. 27, Issue 13, pp. 2262-2275, (2019) (PubMed).: "Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome." in: Journal of inherited metabolic disease, Vol. 31 Suppl 2, pp. S303-11, (2011) (PubMed).
Aliases for IDS 抗体
iduronate 2-sulfatase (IDS) 抗体iduronate 2-sulfatase (CpipJ_CPIJ004938) 抗体
iduronate 2-sulfatase (ids) 抗体
iduronate 2-sulfatase (Ids) 抗体
AW214631 抗体
mps2 抗体
MPS2 抗体
sids 抗体
SIDS 抗体
zgc:158245 抗体
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