NAGLU (NM_000263) Human 3' UTR Clone

Specifications

Product Data
Product Name	NAGLU (NM_000263) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CMT2V; MPS-IIIB; MPS3B; NAG; UFHSD
ACCN	NM_000263
Insert Size	241 bp
Sequence Data	Insert Sequence (showhide) >SC202669 3’UTR clone of NM_000263 The sequence shown below is from the reference sequence of NM_000263. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TACCCCCGCTGGGTGGCCGGCTCTTGGTGATAGATTCGCCACCACTGGGCCTTGTTTTCCGCTAATTCC AGGGCAGATTCCAGGGCCCAGAGCTGGACAGACATCACAGGATAACCCAGGCCTGGGAGGAGGCCCCAC GGCCTGCTGGTGGGGTCTGACCTGGGGGGATTGGAGGGAAATGACCTGCCCTCCACCACCACCCAAAGT GTGGGATTAAAGTACTGTTTTCTTTCCACTTAAA 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_000263.4
Synonyms	CMT2V; MPS-IIIB; MPS3B; NAG; UFHSD
Summary	This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate. [provided by RefSeq, Jul 2008]
Locus ID	4669
MW	8.7

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