PGM1 (NM_002633) Human 3' UTR Clone

Specifications

Product Data
Product Name	PGM1 (NM_002633) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDG1T; GSD14
ACCN	NM_002633
Insert Size	600 bp
Sequence Data	Insert Sequence (showhide) >SC207769 3’UTR clone of NM_002633 The sequence shown below is from the reference sequence of NM_002633. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGACGCACTGCACCCACTGTCATCACCTAAGAAGACAGGCCTGATGTGGTACGTCCCTCCACCCCCGGA CCCATCCAAGTCATCTGATTGAAGAGCATGACAGAAACAAAATGTATTCACCAAGCATTTTAGGATTTG ACTTTTTCACTAACCAGTTGACGAGCAGTGCATTTACAAGGCACTGCCAAACAAGATGCCCTTGGGAGC TGTGAGGGAAAGAGGACCTGCGGGCTTAGATCAATCTCAATTCCTTTTCATGCCCTCCTGCATTGCTGC TGCGTGGGTATTTGTCTCCTTAGCCATCAGGTACAGTTTACACTACAATGTAAGCTATAGGTGGAGCAT CAGCAGTGAGTGAGGCCATTCTTCATCCTTAGGATGTGGCAATGAAATGATGGTGCAAGTTCCTTTCTC TTTTGTGAATCTTTCCCCCCATTTCCTGTTTACATGTAACCCAACAAAATGCAATTTCTAGTGCCTTCT GTCCAATCAGTTCTTTCCTCTGAGTGAGACGTACTTGGCTACAGATTTCTGCCTTGTTTTGCGACATTG TCCCATTCACACAGATATTTTGGGATAATAAAGGAAAATAAGCTACAA 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_002633.3
Synonyms	CDG1T; GSD14
Summary	The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]
Locus ID	5236
MW	22.5

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