GALT (NM_000155) Human 3' UTR Clone

Specifications

Product Data
Product Name	GALT (NM_000155) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_000155
Insert Size	616 bp
Sequence Data	Insert Sequence (showhide) >SC201242 3’UTR clone of NM_000155 The sequence shown below is from the reference sequence of NM_000155. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGGACAGGGAGACAGCAACCATCGCCTGACCACGCCGACCACAGGGCCTTGAATCCTTTTTTGTTTTC AACAGTCTTGCTGAATTAAGCAGAAAGGGCCTTGAATCCTGGCCTGGAATTTGGGCAGATATAGCATTA ATAAAACTGTGCATCTCAAACTTTTATCACATACTCTAATATCAGAGGAGTGTGAACCTTCAGAGATCT AGGGTTAAAAGCTAAAGGCATAGCTCCAGCTACAACTTTTCTTTGTCTACAGATGTGTAAAATCTTGAT GCAAAAATCTACCCCAAATTTCTGAACAAAATTAATATTCAGTATTATATCTAGCCTATAGATTCTCTT ACTCTTGGTGTAATGACAGCATTCCCAGTTTAGGAAACTGTTTTAAAATCTTGTGTCTTGGTTGTGGCT GAGGCTTTGGGAAGGCCAGAGCCCCCTTTGCCACCACCCCTAGGGTGTCAGCTCCAAGCCTGGGCCTGA GGGTTTGATGGGGAGCGGGTGAGCTGGATCCTGATCCCAGTGGTCAGTGGCCAGATCCTGGGCTGCTGG CCAGAACCCTGGCTTTGTGAGTGGCTGCAGCTTGGCTCTGCTCCAGCCCACAGGGGCTAAAGGG 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_000155.4
Summary	Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Locus ID	2592
MW	23.1

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