Kir6.2 (KCNJ11) (NM_000525) Human 3' UTR Clone
CAT#: SC215940
3`UTR clone of potassium inwardly-rectifying channel subfamily J member 11 (KCNJ11) transcript variant 1 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | KCNJ11 |
Synonyms | BIR; HHF2; IKATP; KIR6.2; MODY13; PHHI; PNDM2; TNDM3 |
ACCN | NM_000525 |
Insert Size | 1689 bp |
Sequence Data |
>SC215940 3'UTR clone of NM_000525
The sequence shown below is from the reference sequence of NM_000525. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CCAAGTTCAGCATCTCTCCAGATTCCCTGTCCTGAGCCATGGTCTCTCGGGCCCCCCACACGCGTGTGTA CACACGGACCATGTGGTATGTAGCCCGGCCAGGGCCTGGTGTGAGGCTGGGCCAGCCTCAGCTCAGCCTC CCCCTGCTGCTCATCCAGGGTGTTACAAGGCACTTGTCACTATGCTATTTCTGGCCTCAGCAGGAACCTG TACTGGGTTATTTTTGTCCCTGCTCCTCCCAACCCAATTCAGGACTGGCTCACCCCTCTCCCCCGCCCAA GGCTGCAGAGGCTGTGGGAGGTACTGGGCCCTAGAGCTGTGCGTCCAGCCAGTCCTGGGTCCCCACGATT GACCAGCCACACTCTGGGCCGGTGGCTGGGGAAGAACAATCCCCGAGGGCTGCTGCTTTGCGTCTGTGGC TCCAAGAAGTGCCTGTGGTCAGGCCCCAGCTCTACTTGGTCCCTGAAAAAGCACCTGGCTAAGGGCTGGG CCTGGCCAGCAGGGAGGGCAGTTGATGAGAGAGGGTGTTCCCGCTGGAGGGTTGGTGCTGTGGAGCCTAC ACCGGCAGGGACAGCCTGGGGCTGACAGGGCTCCCCTCCGAGGGCCAGTTTCAGGTCTGGAAGGGGAGGA AGCAGGGGAAGGTGACCTGAGGAGGCTCGGCTTTGTAGAGCCCCGCTCAGGCACAGGGAGGAGGAGATGC CAGGGCTCCTGCCTTTTGCCACATCGGCCTCGTGCAGTGAGGGCTCTGTGGGCTGGGGCTGCTGCCCCTG CCTACCTCCTGCCTGTCCCCAGAGGCTGAGGAGAGGGGGTACTGTGCCCACCACACATGATTAGGCCTCA GACCCAACTCTGGTCCTGGCTCCACAACAGTGGCTGCCACTCACTTTGTCCAGAAGGTGGCTTGGGGGTG GATATCTTTGGGTTGCTGGAAAAGGTGTGGGAAGGTTCAGGATGGTGGGAGGGACTGAGGTCCCTGAGGT GAAGAGGCCCTTGGTCCTGACGGGTTTGACCCGTGCCTGGACCCTTGGAGCAGTGTTGTGTGAACTTGCC TAGAACTCTGCCTTCTCCGTTGTCAATAAAGCCTCCCCCTCATGACCTAAACTCTGGGCTTTTCTTGCTG GGGAGGCAGCAAGCATGCTGGTGGGAAGGGAGGCAGGGACTGGCAGCTGCCACCCCCTTCAAGAGGCGCC ATAGACCCTAGCGGGGAGGGCAGGGGAGGGACGGAAGGCTGGCACCTCTTCCACCAGTTCAGGGGGACTT TCCCCTCTCCTGTCTCAGGTGGCCCAGCCCTGTCAGCCTGTCTGGCCAACTCAGCCTTTGGGCACTCACC AGGCTTTGCAGCCCTGGGCTCTGTCTCTACTCCCAGGGACCTGCTGGAAGGCTGGAGTGCCCAGGGAGAG GTATAGAGGTGTCATAGGCATTAGTGTAGTAATTGGAGCACTAACTCTCGAGCCAACTGCCTGGGTTCGA ATCCTGGCTCTAGCTGTATGACTTTTGTCAAGTAACTTAGCCTCTCTGTGTCTCAGTTGCCTCTTCTATA ACATGGATGCTAATAGTACCTACCTCATAGAATTGTTTTGGAAGTAAATGAAAAATATGTAAAATGCTGA AGTGCCTGGTCTACAGTAAGTGCTCAATAAATGTTAACTATTGTGATTGCTGCTGAATCAGCTACATGCT GAGGAAACG CGGACCGTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
Restriction Sites | SgfI-RsrII |
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). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data | |
RefSeq | NM_000525.3 |
Summary | 'Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2009]' |
Locus ID | 3767 |
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