PRMT5 (NM_001039619) Human 3' UTR Clone

Specifications

Product Data
Product Name	PRMT5 (NM_001039619) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HRMT1L5; HSL7; IBP72; JBP1; SKB1; SKB1Hs
ACCN	NM_001039619
Insert Size	405 bp
Sequence Data	Insert Sequence (showhide) >SC205104 3’UTR clone of NM_001039619 The sequence shown below is from the reference sequence of NM_001039619. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACAGGCCGCTCATATACCATTGGCCTCTAGCCCTGCGTGCCAAGTGTCCAGAGCCTTGGAAGCAGCTTC AGGTTCTGCTCCTGTAGTACAGAAGGTGCAGTACATCTATGGGCTGTGATTCCCCTTGCCCATCAGAGA GGAGCATTTCAATCTGCTTTCCTGCCTTACATCAAGGTGGGCAAGGGATTATAATTAATTGCAGGGCTC AAGCCACCAATCTATGAAGACCTCAGGCCAGGGGGTGAGGAATTAGTGCTGGATTTGAAGCTACGCACT CAGCCTCAAGAACTCCCTGGAATATCCCTGAGAACATGGGGTTTGAACGGATTTTCAGCCTTTTTCTGT TCTTGTTTTGATGGTTTTGTGTAAGAGGAAATACAAATAAAGTTATAGCCCTTTACTGCA 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_001039619.3
Synonyms	HRMT1L5; HSL7; IBP72; JBP1; SKB1; SKB1Hs
Summary	This gene encodes an enzyme that belongs to the methyltransferase family. The encoded protein catalyzes the transfer of methyl groups to the amino acid arginine, in target proteins that include histones, transcriptional elongation factors and the tumor suppressor p53. This gene plays a role in several cellular processes, including transcriptional regulation, and the assembly of small nuclear ribonucleoproteins. A pseudogene of this gene has been defined on chromosome 4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]
Locus ID	10419
MW	14.8

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