The following RNASEH2C gene sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the RNASEH2C gene which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
||Documents for ORF clone product in dufault vector
||ORF Nucleotide Sequence (Length: 495bp)
||pcDNA3.1+/C-(K)DYK or customized vector
||Document: User manual_GenEZ ORF Clone Products.pdf (pdf)
|Tag on pcDNA3.1+/C-(K)DYK
||C terminal DYKDDDDK tags
||Document: MSDS_GenEZ ORF Clone Products.pdf (pdf)
|ORF Insert Method
||CloneEZ® Seamless cloning technology
||Homo sapiens (human)
||ribonuclease H2 subunit C
||REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AF346606.1, BC023588.2,
AP001266.4 and BC000831.1.
This sequence is a reference standard in the RefSeqGene project.
On Aug 25, 2006 this sequence version replaced gi:38176284.
Summary: This gene encodes a ribonuclease H subunit that can cleave
ribonucleotides from RNA:DNA duplexes. Mutations in this gene cause
Aicardi-Goutieres syndrome-3, a disease that causes severe
neurologic dysfunction. A pseudogene for this gene has been
identified on chromosome Y, near the sex determining region Y (SRY)
gene. [provided by RefSeq, Jul 2008].
Transcript exon combination :: AF346606.1, BX353248.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
COMPLETENESS: complete on the 3' end.