COG2 (NM_001145036) Human 3' UTR Clone

Specifications

Product Data
Product Name	COG2 (NM_001145036) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDG2Q; LDLC
ACCN	NM_001145036
Insert Size	619 bp
Sequence Data	Insert Sequence (showhide) >SC208059 3’UTR clone of NM_001145036 The sequence shown below is from the reference sequence of NM_001145036. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGGACCAGGCAACAGCAGAGCAGCCTTAAGCATCTTGGAAGATCCCGAGGTTAGATTCTTAAGCAAGA GAAGAGTTGGACTTCCAGGCTGAAGGGGAGAAAGTGACTCTGTTCTCTTAGCAACCGTCTGTAGCAAAG AAGTGCTTCCAGCATCACTCCAGCAACACGCCCATGCGTCTTCTCTCAGCGTATTTGGGTCTTCTTTGC CCAAAAGAACACAAAAGCCTTTTTCCATTGTATGGAAGATAGTTTTTAAGACATTTGAAACTTTCTACT ATAGTTTACAGAACAAATTATTTTATTTTTATTGTAAATCTTAGTGTGGAAGAGCTGATTTCTAAAATA TGATTAAAGTAAATATATACCTATGAATATCAAGAGTCGTCTCCCTGAGCCTGTAGTTGGAAGTGACGA CTGTAATGGAATGATGTCTTGTATAGAAATGCCCTTCTCTGAAATAAAGAGAACTCCTGGGCTTTCTAA AGAGGCTGCGGGAAGCCATCCTCCACTCCCACTGTGTGTGAGAGCAGTGCTTCTGATCCTGCTGTCACC CCGACCTCTGGCAGGAGCCGGCGCCAGTAGGAAAGACCTCCTTCCTAAATAAAAGAAGTGTCTCCCA 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_001145036.2
Synonyms	CDG2Q; LDLC
Summary	This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi complex. The encoded protein specifically interacts with the USO1 vesicle docking protein and may be necessary for normal Golgi ribbon formation and trafficking of Golgi enzymes. Mutations of this gene are associated with abnormal glycosylation within the Golgi apparatus. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]
Locus ID	22796
MW	23.6

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