Iduronate 2 sulfatase (IDS) (NM_006123) Human 3' UTR Clone

Specifications

Product Data
Product Name	Iduronate 2 sulfatase (IDS) (NM_006123) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ID2S; MPS2; SIDS
ACCN	NM_006123
Insert Size	187 bp
Sequence Data	Insert Sequence (showhide) >SC202029 3’UTR clone of NM_006123 The sequence shown below is from the reference sequence of NM_006123. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CATGGTTTCCTCATGAGGACAAATACCTGATTTTGAATAAAGCAGCATTCAGTTGAAATAACCCTTTCT GTGGTAATTCCAAGTGAATATTTTTCTTCTAGGTGATGAGTTTCTACTTCCTCTGGTTTTTACAACAGG AAATGAAATGGTATCTAAAATAAACAAGCTGTGGTATGATGATTATTCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_006123.5
Synonyms	ID2S; MPS2; SIDS
Summary	This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]
Locus ID	3423
MW	7.1

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