KCTD1 (NM_001142730) Human 3' UTR Clone

Specifications

Product Data
Product Name	KCTD1 (NM_001142730) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	C18orf5
ACCN	NM_001142730
Insert Size	841 bp
Sequence Data	Insert Sequence (showhide) >SC210359 3' UTR clone of NM_001142730 The sequence shown below is from the reference sequence of NM_001142730. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CGGATAAAGCAAGAGCCTCTGGACTAAATGGACATATTTCTTATGCAAAAAGGAAAACACACACAACCAA TAACTCAAACAAAAAAGGGACATTTATGTGCAGTTGGGACAGCAAACCAAGTCCTGGACGTAAAATCGAA TAAAAGACACATTTATATCCAATAGAGACCACACCTGTATTCATATGGGAACAATTGGAATAGTGATATC CTCAAGGTGTAAAAAATATATAAATATATATATATATGTCAAAAGGTAGGAAATGCAAAAAAGAAAAAAA AAAAAGGTGACAGCCGCAGTTGGTGCTGTGATGGCCGTGAAGTGTCCTGGGCCTTCCGAGGCCTCTGACA AATAAACAAGCCATGAGTGGTGAGGACACAGTCTCCTTACAGTTTCCATTGCCAACAACAGCCATCCATA TTTCTTTTTTCCTTTGTCTTTCTTTTTCCTTTTTTTTTAAAAAAACAAAACAAACAAAACACCTTGAATC AAGTTTGTTTGTATATGGAGGTTCCACGTCTTTCTTTAGGCAGGGACCAGGCAGGACTTCAGAAAAACCC TCATGAGCACATTGCAAAGATGTTAGACATGAAATTTTAAATGTAGTTTGTACAGAAGTCACACTTTTTT GTCCACCTCACAGATGTGAACTTTACTTTGTTTTAAAACTGATCAGTTTTGCCAAGGGGCCAGAATTATT CCTTGTTAGAATTGCTCCAGTTCAAGTCTGCTGCTTTCCTACAATTTTTCAAATTTTATAATGTATTAAA TACAATAAACTCTGTTTAAAAAATAAGGTCTGTGTGAAACACACATGTGGGGGTGAGGCTGGATTAAAGT G ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_001142730.1
Synonyms	C18orf5
Summary	This gene encodes a protein containing a BTB (Broad-complex, tramtrack and bric a brac), also known as a POZ (POxvirus and zinc finger) protein-protein interaction domain. The encoded protein negatively regulates the AP-2 family of transcription factors and the Wnt signaling pathway. A mechanism for the modulation of Wnt signaling has been proposed in which the encoded protein enhances ubiquitination and degradation of the beta-catenin protein. Mutations in this gene have been identified in Scalp-ear-nipple (SEN) syndrome. [provided by RefSeq, May 2017]
Locus ID	284252

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.