DNA Polymerase gamma (POLG) (NM_001126131) Human 3' UTR Clone

Specifications

Product Data
Product Name	DNA Polymerase gamma (POLG) (NM_001126131) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MDP1; MIRAS; MTDPS4A; MTDPS4B; PEO; POLG1; POLGA; SANDO; SCAE
ACCN	NM_001126131
Insert Size	461 bp
Sequence Data	Insert Sequence (showhide) >SC206237 3’UTR clone of NM_001126131 The sequence shown below is from the reference sequence of NM_001126131. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTGGAAAAACGAAGCCAGCCTGGACCATAGCACTGCCTGGAGGCTCTGTATTTGCTCCCGTGGAGCTTC ATCGGGGTGGTGCAGGCTCCCAAACTCAGGCTTTCAGCTGTGCTTTTTGCAAAAGGGCTTGCCTAAGGC CAGCCATTTTTCAGTAGCAGGACCTGCCAAGAAGATTCCTTCTAACTGAAGGTGCAGTTGAATTCAGTG GGTTCAGAACCAAGATGCCAACATCGGTGTGGACTACAGGACAAGGGGCATTGTTGCTTGTTGGGTAAA AATGAAGCAGAAGCCCCAAAGTTCACATTAACTCAGGCATTTCATTTATTTTTTCCTTTTCTTCTTGGC TGGTTCTTTGTTCTGTCCCCCATGCTCTGATGCAGTGCCCTAGAAGGGGAAAGAATTAATGCTCTAACG TGATAAACCTGCTCCAAGGCAGTGGAAATAAAAAGAAGGAAAAAAAA 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_001126131.2
Synonyms	MDP1; MIRAS; MTDPS4A; MTDPS4B; PEO; POLG1; POLGA; SANDO; SCAE
Summary	Mitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N-terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO), Alpers-Huttenlocher syndrome (AHS), and mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID	5428
MW	17.2

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