UFD1 (NM_005659) Human 3' UTR Clone

Specifications

Product Data
Product Name	UFD1 (NM_005659) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	UFD1L
ACCN	NM_005659
Insert Size	789 bp
Sequence Data	Insert Sequence (showhide) >SC209327 3’UTR clone of NM_005659 The sequence shown below is from the reference sequence of NM_005659. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCATTGCGTAAAAAGGGAAGAAAGCCCTAAGTGAGGACTGTTGGCTGATTGGAAAATAATAAAAGAATC ATTTGCAACATCTTGGCTTTTAGTTACTGGCACTGACAGGGACGAGCCTCATCAGAGAATACTCTGTTA CTTAAGATTTATTTAGAGTTACCTAAGAATTATTAAGTTTGACTTGGAAGTGGAGCAGCAGGACTTTGT AGTTGTATGCTTGATTTGGGGAAAGACAAAGAGCTGTCCCTGAGGGCCTGTAGATAGCTGCCTCCTCAC CTCTTCACGCTTTCAGCTTGAGGGGAGCTCCCACTGCCTCAGCAGGAGCAATTCTGCATCCCTAATTCT GTCAAAACCTATGAAGGTGACTAAATTGTCTAACATGAAGTGTTCTTTCTTTTTCTTCATTTATCCTTT CTTTTCCTACATCAATTGCATAGGTGTCAGTCTTTGGCCTAAAAAAAGGCTTTAAATAGACATGTGTTC TATAAGTAGTGGCTGTCCCACTACTGTGGCTGCAATTTAAGTATTTGACAAAGAATGTTTCTATTTTTA TTTTACATATTTTTTTCAAAAACACCACTCAGAAGAACCTGATCTGAATGAGTTTGCACTTTTATTCTC ATTTCATATGGACATAACTGGCTCCTTAGTGAACCTGTTCATAGTGAAACAACTCCATGGAGAAGCAAA CATGTGAATGTTAGAATGAACAAATGCTAAAGAGATGTTCCTCTCCTTCTTCCCTACTCCCCAACTCCC AATTTTAATTTATTAAATCATCCAAGCTTC 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_005659.7
Synonyms	UFD1L
Summary	The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Jun 2009]
Locus ID	7353
MW	30.6

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