RNASEH2B (NM_001142279) Human 3' UTR Clone

Specifications

Product Data
Product Name	RNASEH2B (NM_001142279) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AGS2; DLEU8
ACCN	NM_001142279
Insert Size	542 bp
Sequence Data	Insert Sequence (showhide) >SC206953 3’UTR clone of NM_001142279 The sequence shown below is from the reference sequence of NM_001142279. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCAGCACAAAGACAGAAAAGGGGCAAGTGATGGTGGTGGCTCCACGCAAGGCTTGGCGGTTTTCCCTGC AACTTCAGACACTCCCAGAGGACTCGGACTTTTTCTTCTGCACTTTTTTGGAAAATCGCCAGGTGCCAA AAGGTGCATTTTAAAGCGCTGACTGTAAATGCTTTATTTCTTTGATTAGTACCACTAGTCTATGTGGGC AGCGGCATTCCTCCCTGGAGCACTCAGCTAGGCGGTTCCGTCCAGGAGCTTGAAAGCATCCCAGCGGTG CACCTGTTCAGTCTGAGGACCTCAAGCTTGGGTCAGGCCAGCATGTTTTAGGTATGGATGTGGTGACTT AAAGTACTTGATTGTCTTGATTTCACCCTGAAAGCTTTGGCAAACCAAGTTTCAACCCTTACTTTAAAA ATCTGACACTGCTTTACTCCATATCAATTTGGAAGCTTCTAATTCATAAATATACCTAAACGTTGGCAT TTTATCTCTCCAGGAGTTATTAAACATTTCTTCCTTTTTAGAAAAAAAAAAAAAAAAAA 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_001142279.2
Synonyms	AGS2; DLEU8
Summary	RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]
Locus ID	79621
MW	20.9

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