FARS2 (NM_006567) Human 3' UTR Clone

Specifications

Product Data
Product Name	FARS2 (NM_006567) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	COXPD14; FARS1; HSPC320; mtPheRS; PheRS; SPG77
ACCN	NM_006567
Insert Size	184 bp
Sequence Data	Insert Sequence (showhide) >SC201458 3’UTR clone of NM_006567 The sequence shown below is from the reference sequence of NM_006567. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCTGTTGGGTGTGGAGGGCAGGTTCTGATGTCACCACTTCACTCAGGCTGCAGCCCTCTTGGGGCTC CAGGATTTGCTGAAAGAGAAAAAGATATGGTTTGTGAACTGGGGCATCAATCATCTTTTGATAAATGGA TCAGTTTTAGGACTTTCAGAAAATAAAAGATCGCTCTTGAAAAGCT 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_006567.5
Synonyms	COXPD14; FARS1; HSPC320; mtPheRS; PheRS; SPG77
Summary	This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Locus ID	10667
MW	6.9

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