KCNQ3 (NM_004519) Human 3' UTR Clone

Specifications

Product Data
Product Name	KCNQ3 (NM_004519) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BFNC2; EBN2; KV7.3
ACCN	NM_004519
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC203132 3’UTR clone of NM_004519 The sequence shown below is from the reference sequence of NM_004519. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTATGGACCCCTTCCAATAAGCCCATTTAAAAGAGGTCACTGGCTGACCCCTCCTTGTAATGTAGACAG ACTTTGTATAGTTCACTTACTCTTACACCCGACGCTTACCAGCGGGGACACCAATGGCTGCATCAAATG CATGCGTGTGCGTGGTGGCCCCACCCAGGCAGGGGCTTCCCACAGCCTCTTCCTCCCCATGTCACCACA ACAAAGTGCTTCCTTTTCAGCATGGTTTGCATGACTTTACACTATATAAATGGTTCCGCTAATCTCTTC TAGGATACACATTTATCTGCTGTTCTTACTTTTAATCACGATTGGACCAGTACAGGGAGAAATTACTGA TGAGCCATGCTATTTGTCTGTTTGGTTGGCTGGTTTGGGTTTTGGTTTGGTAAGCAGAGAAAGTAGTTT AAGTTATTTCTAGGATCACTGCCCTCTTGTGTAAAACGCTCCAGCAATTAACTGTTTTTGAAAGCAAGG AAATAATTTTCTCAACAAAACCACATTGTGTATCAGTGGGGCTGCCTACTGAGCTAACATTAGGAAAGG AATGAGATAGTCATTGTGTCTCTAAAACAAAGAATTTAAACAAATATTTAAGGCAAAACCTTTTAAAAG CTCTCCAAAAGACCTCACTTGGCCTGATGTTACTTAGTATCATGCCTCAGTTTCCTTATCTGTAAAAAG TGGTGGTAATCCCAAGTGTAGCATTTCTGATGAGTTATGAATTGGCAGGGAGAAAACACACACACACAC ACACACACACACACACACACACACATACACAAAGTTAAAATAGTTTCCAATTTATGTAGCCAAGGACAA TGGAATTTATCAGAAGTGAAGTGCCCCTCTGGGCAGGAGCTGAGTTCAGTGCCTTTAAAATGAATTTCC AACTCTCATTTCTTCCCATGATACTGAAGTACAAAATATCCATCTAAAATAGAAATTAAAGTCAAGAAG GCACACAGAAATTTTCTAGTCCAAGGACTTCCTTTTATAAATGAAGAATCTTAGGCTCAGGTAAAGTGA CATACCCAGAGTCACTCAGTTGTCCCATAGAGAACCAGGACTCAAAAGTCAGGTCTGCCCACTCTCCCT GACCTTGTTTCCCCTCACCACACCATTCTTCCATTTATATAATGCATCCTAGAGATTGTGTCAAGATAT ATGACTTTGTGTCGCGTGGAAAGCACCCAGTTTATCCAGCAGGAGGGGGATTTCCACTTTTATTGCAAA ACATGCTTGCTTGATGCAATGCATTTCAGATCTAGAAAAAAATAATGCAAGCAAGCTACATTTACAGAT GTGTAAACAGGCAAAATTTCCAGAACCGTCCAATTTTACTTTTCCAAATTTATGGAACCAACCCAGATT TTTTAAATGAAAATACTAAAACCATATGTAACCGTAAGACAAGCTAAAATGTAAGCAGACAGCCTGGGA AGCACTGCCCTACTGTACAGGTGTGATATTAAGCACAAGCCATCCTCTGGCCTCTTATGAGATGTTGTT ATTCTCTGAAAAACTTTGATGGAAAAGGTTTCTGTTAGGCTTAGACTGAATTAGCTAAATGACCATGCC ACAGTATTATTGTATCACTCTTCTCACACACCTAGGCACTGGTTGTGGATAGTTGCCATGGTGACAATC AAGATAATCCAGATGACCTAAACAAATGTCTGTATGCAGCTGACACTGCTATTCTCCCTCACAGTCTTG TCAAGAGCCACAGTAGCTATGGCAGACATTTGGTTGATGGTTTCATCATTTCCTAATACGAGAGTCTGG CACTATGTTGGAGAGAGGAATCACTTCCTCAGAGATAGGTTCCTTTCAACTCACATGTCAACAGTTACT GTACAAAAAGCTCAGAATACAGTAATGATTAGAGCTTGACCCCTGACTTTAGGAACTTAGAACCAAAGC CCAAAGTCCCAGGCCAAGGGCAGACATTGTGAGCAGCAGAAGGGTGTTTTTTATGGAGAGCCCCATAA 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_004519.4
Synonyms	BFNC2; EBN2; KV7.3
Summary	This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]
Locus ID	3786
MW	77

*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.