PGD (NM_002631) Human 3' UTR Clone

Specifications

Product Data
Product Name	PGD (NM_002631) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	6PGD
ACCN	NM_002631
Insert Size	792 bp
Sequence Data	Insert Sequence (showhide) >SC205308 3’UTR clone of NM_002631 The sequence shown below is from the reference sequence of NM_002631. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACCGTGTCATCCTCGTCATACAATGCCTGATCATGCTGCTCCTGTCACCCTCCACGATTCCACAGACCA GGACATTCCATGTGCCTCATGGCACTGCCACCTGGCCCTTTGCCCTATTTTCTGTTCAGTTTTTTAAAA GTGTTGTAAGAGACTCCTGAGGAAGACACACAGTTTATTTGTAAAGTAGCTCTGTGAGAGCCACCATGC CCTCTGCCCTTGCCTCTTGGGACTGACCAGGAGCTGCTCATGTGCGTGAGAGTGGGAACCATCTCCTTG CGGCAGTGGCTTCCGCGTGCCCCGTGTGCTGGTGCGGTTCCCATCACGCAGACAGGAAGGGTGTTTGCG CACTCTGATCAACTGGAACCTCTGTATCATGCGGCTGAATTCCCTTTTTCCTTTACTCAATAAAAGCTA CATCAGACTGATGCTCTTTCTCCAGATTCTTAGTCTCACCTCGGCCACATGGAGCCATTATCCCCATTG GCAGAAAGATTTTTCTTTAAAAAAAAAGACTAGAATAACACAAGAAACCACATTTAGGATTATGCTTCA CTCAGAGGAGGCAGGCAGGGAGGACACACCAGGGGCTTTAATACACTGGGCATGTTTTCTTTCTCCAAT TGGGCAATGGGTACATGGACGTTCACTGTAACGTGCTTTTTCTTTCGTCTTTTTTTTTTTTTTTTTTTT TTTTGCTCCTGGCAAGCTGTGCGTGACATTCTTTATGGCTTTTTGTATGTCAAATACTTCATACTAAAC TTTCTAGAGAATTAAACTTTAATGATGGGCTCA 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_002631.4
Synonyms	6PGD
Summary	6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
Locus ID	5226
MW	30.1

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