VCP (NM_007126) Human 3' UTR Clone

Specifications

Product Data
Product Name	VCP (NM_007126) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDC48; FTDALS6; p97; TERA
ACCN	NM_007126
Insert Size	1083 bp
Sequence Data	Insert Sequence (showhide) >SC212068 3’UTR clone of NM_007126 The sequence shown below is from the reference sequence of NM_007126. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAAGACAATGATGATGACCTGTATGGCTAAGTGGTGGTGGCCAGCGTGCAGTGAGCTGGCCTGCCTGGA CCTTGTTCCCTGGGGGTGGGGGCGCTTGCCCAGGAGAGGGACCAGGGGTGCGCCCACAGCCTGCTCCAT TCTCCAGTCTGAACAGTTCAGCTACAGTCTGACTCTGGACAGGGGGTTTCTGTTGCAAAAATACAAAAC AAAAGCGATAAAATAAAAGCGATTTTCATTTGGTAGGCGGAGAGTGAATTACCAACAGGGAATTGGGCC TTGGGCCTATGCCATTTCTGTTGTAGTTTGGGGCAGTGCAGGGGACCTGTGTGGGGTGTGAACCAAGGC ACTACTGCCACCTGCCACAGTAAAGCATCTGCACTTGACTCAATGCTGCCCGAGCCCTCCCTTCCCCCT ATCCAACCTGGGTAGGTGGGTAGGGGCCACAGTTGCTGGATGTTTATATAGAGAGTAGGTTGATTTATT TTACATGCTTTTGAGTTAATGTTGGAAAACTAATCACAAGCAGTTTCTAAACCAAAAAATGACATGTTG TAAAAGGACAATAAACGTTGGGTCAAAATGGAGCCTGAGTCCTGGGCCCTGTGCCTGCTTCTTTTCCTG GGAACAGCCTTGGGCTACCCACCACTCCCAAGGCATTCTTCCAAATGTGAAATCCTGGAAGTAAGATTG CACCTTCTTCCTCTCCTGATCAACATCGGTATGATGTCTCCTGTTGCCTCACCCTTTGTCTGCAGTATC ACTGGATAGGACTGGTGGAAAGGGAGCAGCCTGACAGAGCTCCAAATGTGGAGAATATGGCATCCCTCC ACCTATATTTGATGTGGACGGTAAGGCTAGGCCTGCAGGATCCCTTATCCTGACCAAAGACTGTGTTGG GGTGCCATTTGAAAATCGCAGGGTTGCAAAAGAATACAATCTTACTTGCAGGTGGATATTCTCTATACT CTCTTTTAATGCATCTAAAAATCCCAAACATCCCCTGGTTGGTGATCACTTACAGTTGTGTCCACCTTT ATTTTATGTACTTTGATTAAAAAAAAAAAACTTTTTGTTAATATAAAA 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_007126.5
Synonyms	CDC48; FTDALS6; p97; TERA
Summary	This gene encodes a member of the AAA ATPase family of proteins. The encoded protein plays a role in protein degradation, intracellular membrane fusion, DNA repair and replication, regulation of the cell cycle, and activation of the NF-kappa B pathway. This protein forms a homohexameric complex that interacts with a variety of cofactors and extracts ubiquitinated proteins from lipid membranes or protein complexes. Mutations in this gene cause IBMPFD (inclusion body myopathy with paget disease of bone and frontotemporal dementia), ALS (amyotrophic lateral sclerosis) and Charcot-Marie-Tooth disease in human patients. [provided by RefSeq, Aug 2017]
Locus ID	7415
MW	39.9

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