ARD1A (NAA10) (NM_003491) Human 3' UTR Clone

Specifications

Product Data
Product Name	ARD1A (NAA10) (NM_003491) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ARD1; ARD1A; ARD1P; DXS707; hARD1; MCOPS1; NATD; OGDNS; TE2
ACCN	NM_003491
Insert Size	792 bp
Sequence Data	Insert Sequence (showhide) >SC200566 3’UTR clone of NM_003491 The sequence shown below is from the reference sequence of NM_003491. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCTCAGAGGCCTCCGACTCAGCCTCCTAGAGCCTGCCCCATCCCCTCCTCACCCCACGAGCTTTCACA ATAAATTCGCTCCGTGGCACTGGGGAACTTTGTGTGTGAGCGCGCGCACATTTAGAGGGTGTGTTTCTC CAGGTCCTCTGGTGGGGATGTGAGCCTTGGCCTTTTGACCCAGAGCATCCTGCCAGGCCCGAGTACAAG GAAAGAGCTTTGGAGGTGGGACTCCCTAGTCTCATGACCTTCAGCAGCTGTGGCCCCGGGGAAGGAGGC CCTGGACTTATGGGAGAGACCCTGCCTTGGAGGTCTGCTTGGCCACGCTGAATGTGTTTTGTGGCACAA GCCGGGGCTGCTCAGGCTCAAAGCTCAACAGCAGGGCTCCCACTCTTGGTGGCCTTCAGTTCTCTTCCC ACCTTCACCTTCAGACTTTCTCTCCCTAATCACACCTGCTTCGGGCTACAGCAGCTCCCCAGCATACCC GTGGGCTCCAGATGTGGACATCCAACTGCTCATTGGGCTTATCTACAAATGTCCTGTCTGAGTAATGAC CCAGCCAGATGCCCCATCAACAGTCCTTGAGTCCTCCCTCCCCTGCCACCCTAATGGTCAGTGAGTCCA TGATACCTCTTGAGTCTACTCCCTAACCTGAGTTTGCATTTGAAAATAATTTATTTTTAGTACAATTCC CCGCGTTTCCCCATTGACATTTTGTATTAGTTGGTGTATTTGTTATTGTTGATGCGCCAATACTGATAA GTTATTGTAAACTACAGCCCATGGTTTACAGTA 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_003491.4
Synonyms	ARD1; ARD1A; ARD1P; DXS707; hARD1; MCOPS1; NATD; OGDNS; TE2
Summary	N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Locus ID	8260
MW	29.2

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