NHP2 (NM_017838) Human 3' UTR Clone

Specifications

Product Data
Product Name	NHP2 (NM_017838) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DKCB2; NHP2P; NOLA2
ACCN	NM_017838
Insert Size	280 bp
Sequence Data	Insert Sequence (showhide) >SC203286 3’UTR clone of NM_017838 The sequence shown below is from the reference sequence of NM_017838. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGGTGCAGTCCCTGCCCCTACCCCTATGAGGGGCTCCGGTAGCACCTGGGCACCTGCCGCTGGAAGCT ATTGGGCTGGCAGCAGGACGACTGGCTGTCCTCCTGCCCACCCACACTGACGGCATCTTCCCAGTTCCC CAAGGCACGCCTTCTTCCCAGGCAGCTCTAACAGCCCTTTCATGAAGGTAATGCTAGTCTTCTGTCCAT CAGTGCCATTTCCTGTAGAACTAAAGGCTGTTCCAAGAATGTGGGGTGGGGAAAGTAAATGCTAAGACT AAAA 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_017838.4
Synonyms	DKCB2; NHP2P; NOLA2
Summary	This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA1 and NOLA3 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. The four H/ACA snoRNP proteins are also components of the telomerase complex. This gene encodes a protein related to Saccharomyces cerevisiae Nhp2p. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008]
Locus ID	55651
MW	9.7

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