GCN2 (EIF2AK4) (NM_001013703) Human 3' UTR Clone

Specifications

Product Data
Product Name	GCN2 (EIF2AK4) (NM_001013703) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GCN2; PVOD2
ACCN	NM_001013703
Insert Size	537 bp
Sequence Data	Insert Sequence (showhide) >SC207148 3’UTR clone of NM_001013703 The sequence shown below is from the reference sequence of NM_001013703. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGAGATGACTACTACAGAATCTTATTTTAACCCTAAAGAACTGTCGTTAACCTCATTCAAACAGACAGA GGCTTATACTGGAATAATGGAATGTTGTACATTCATCATAATTTAAAATTAAATTCTAAGAAGAGGCTG GGTGCAGTGGCTCACACCTTTAATCCCAGCACTTTGGGAAGCCAAGGCAGGAAGACTGCTTGAAACCAG GAGTTTGAGACCAGCCTGAGCAACAAAGCAAGACCCCATCTCTATAAAAACTAAAAAAATTAGTTGGGC ATGGTGGCACATGCCTGTAGTCCCAGCTACTCCAGAGGCTGAGATGGATCATCTGAGCCTCAGGAGGTT GAGGCTGCAGTGAGCTGTGACTGCGCCACTGCACTCCAGTCTGGGACAACAGAGCAAGACCCTGTCTTA AAAAAAAAAAGAAAAAAAAAATTTTTTTCTAAGAAGCTGTCCTACAAAGTTGAGCTTTGTTAGTTTTTC ATGTGTAATATATTATAAATTTATCTTTTGGGATATAATAAATGCTTTCATATA 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_001013703.4
Synonyms	GCN2; PVOD2
Summary	This gene encodes a member of a family of kinases that phosphorylate the alpha subunit of eukaryotic translation initiation factor-2 (EIF2), resulting in the downregulaton of protein synthesis. The encoded protein responds to amino acid deprivation by binding uncharged transfer RNAs. It may also be activated by glucose deprivation and viral infection. Mutations in this gene have been found in individuals suffering from autosomal recessive pulmonary venoocclusive-disease-2. [provided by RefSeq, Mar 2014]
Locus ID	440275
MW	20.5

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