RNASEH2B (NM_001142279) Human 3' UTR Clone
CAT#: SC206953
3`UTR clone of ribonuclease H2 subunit B (RNASEH2B) transcript variant 2 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | RNASEH2B |
Synonyms | AGS2; DLEU8 |
ACCN | NM_001142279 |
Insert Size | 508 |
Sequence Data |
>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. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CCATCAAAGATGGCAGCACAAAGACAGAAAAGGGGCAAGTGATGGTGGTGGCTCCACGCAAGGCTTGGCG GTTTTCCCTGCAACTTCAGACACTCCCAGAGGACTCGGACTTTTTCTTCTGCACTTTTTTGGAAAATCGC CAGGTGCCAAAAGGTGCATTTTAAAGCGCTGACTGTAAATGCTTTATTTCTTTGATTAGTACCACTAGTC TATGTGGGCAGCGGCATTCCTCCCTGGAGCACTCAGCTAGGCGGTTCCGTCCAGGAGCTTGAAAGCATCC CAGCGGTGCACCTGTTCAGTCTGAGGACCTCAAGCTTGGGTCAGGCCAGCATGTTTTAGGTATGGATGTG GTGACTTAAAGTACTTGATTGTCTTGATTTCACCCTGAAAGCTTTGGCAAACCAAGTTTCAACCCTTACT TTAAAAATCTGACACTGCTTTACTCCATATCAATTTGGAAGCTTCTAATTCATAAATATACCTAAACGTT GGCATTTTATCTCTCCAG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_001142279.1 |
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 |
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