HCN2 (NM_001194) Human 3' UTR Clone

Specifications

Product Data
Product Name	HCN2 (NM_001194) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BCNG-2; BCNG2; HAC-1
ACCN	NM_001194
Insert Size	715 bp
Sequence Data	Insert Sequence (showhide) >SC209383 3’UTR clone of NM_001194 The sequence shown below is from the reference sequence of NM_001194. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCGCGCTCGCGCCTCTCGTCCAACTTGTGACCCTCGCCGACCGCCCCGCGGGCCCAGGCGGGCCGGGGG CGGGGCCGTCATCCAGACCAAAGCCATGCCATTGCGCTGCCCCGGCCGCCAGTCCGCCCAGAAGCCATA GACGAGACGTAGGTAGCCGTAGTTGGACGGACGGGCAGGGCCGGCGGGGCAGCCCCCTCCGCGCCCCCG GCCGTCCCCCCTCATCGCCCCGCGCCCACCCCCATCGCCCCTGCCCCCGGCGGCGGCCTCGCGTGCGAG GGGGCTCCCTTCACCTCGGTGCCTCAGTTCCCCCAGCTGTAAGACAGGGACGGGGCGGCCCAGTGGCTG AGAGGAGCCGGCTGTGGAGCCCCGCCCGCCCCCCACCCTCTAGGTGGCCCCCGTCCGAGGAGGATCGTT TTCTAAGTGCAATACTTGGCCCGCCGGCTTCCCGCTGCCCCCATCGCGCTCACGCAATAACCGGCCCGG CCCCCGTCCGCGCGCGTCCCCCGGTGACCTCGGGGAGCAGCACCCCGCCTCCCTCCAGCACTGGCACCG AGAGGCAGGCCTGGCTGCGCAGGGCGCGGGGGGGAGGCTGGGGTCCCGCCGCCGTGATGAATGTACTGA CGAGCCGAGGCAGCAGTGCCCCCACCGTGGCCCCCCACGCCCCATTAACCCCCACACCCCCATTCCGCG CAATAAACGACAGCATTGGCGCCAA 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_001194.4
Synonyms	BCNG-2; BCNG2; HAC-1
Summary	The protein encoded by this gene is a hyperpolarization-activated cation channel involved in the generation of native pacemaker activity in the heart and in the brain. The encoded protein is activated by cAMP and can produce a fast, large current. Defects in this gene were noted as a possible cause of some forms of epilepsy. [provided by RefSeq, Jan 2017]
Locus ID	610
MW	24.5

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