KCNH2 (NM_172056) Human 3' UTR Clone
CAT#: SC206549
3' UTR clone of potassium voltage-gated channel subfamily H (eag-related) member 2 (KCNH2) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | KCNH2 (NM_172056) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ERG-1; ERG1; H-ERG; HERG; HERG1; Kv11.1; LQT2; SQT1 |
ACCN | NM_172056 |
Insert Size | 520 bp |
Sequence Data |
>SC206549 3’UTR clone of NM_172056
The sequence shown below is from the reference sequence of NM_172056. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAACAGACACTTTTTGCTTCCTTAAAGTAGGATCAAATCTAGATCCTCTAGCCTGGGCAGTAGAGGAAG AAATGCTAGCCTGGAAGCTCGGCATTTGGTTTCACTAAGGGCCATGTGGTTCCCTGCAGCCTCATGCCT GGCCCCTTGACACATCCAAAGCAAAGGGAGTCCTGCCCCCTCCCCCCACTTCCTTTCTACCCTGCCTGT GCACAGTGGGTGGGTTGGTGTGTCTGGACACTGAGGACTTCCTCCCCCTTTGCCTGTCCTTCCCTCGGC CCTGTGTGCCTCAGGGCAGATATAGCAAGCTCTTTCGACCATAGTTGATGGTAGGACATTTTAGACTTT GTTTCTCAGCTCTGTACAAACACAAATACACACCCCCACAAAACTAAAATCAAAGTTTCACTACATAAC ACTGGGCCTTACTGCATGTGGTTCATTCTAGCATTTCTGTTCTGTGCTGTGCTAAGCTATACTACTGTA TGTTCTTTCAGTAAAAAAAAAAAAAAAAAAAAAAAAA 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_172056.2 |
Synonyms | ERG-1; ERG1; H-ERG; HERG; HERG1; Kv11.1; LQT2; SQT1 |
Summary | This gene encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008] |
Locus ID | 3757 |
MW | 19.4 |
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