Kir6.2 (KCNJ11) (NM_000525) Human Untagged Clone

CAT#: SC321488

KCNJ11 (untagged)-Human potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11), transcript variant 1


  "NM_000525" in other vectors (6)

Reconstitution Protocol

USD 760.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol KCNJ11
Synonyms BIR; HHF2; IKATP; KIR6.2; MODY13; PHHI; PNDM2; TNDM3
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>OriGene sequence for NM_000525.3 GGCAGGGTTGGGGGCTCCCTAGGCGCCAGGCAGGTGGGCTCAAGGGTGAGGCTGTTTTTT
TGTTTTGTTTTTTGTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTG
GCGTGATCTTGGCTCACTGCAACCTCCGCCTCTCGGGTTCAAGCGATTCTCCTGCCTCAG
CTTCCTGAGTAGCTGGGATTACAGGTGCGCACCACCATGCCCGGCTAACTTTTGTATTTT
TAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTAGTGAT
CTGCCCTCCTCAGCCTCCCAACGTACTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCT
GAGGCTGGTATTAAGAAGTGAAGTGGGACCCAGGTGGAGGTAAGGAAGAGTCTGGTGGGG
AGTTATCTCAGAAGTGAGGCCAGCACAGGCTGAGTGCAGCCCCAGGGTGAGAAGGTGCCC
ACCGAGAGGACTCTGCAGTGAGGCCCTAGGCCACGTCCGAGGGGTGCCTCCGATGGGGGA
AGCCCCTCCCTGGGGGTCACCGGAGCCATGCTGTCCCGCAAGGGCATCATCCCCGAGGAA
TACGTGCTGACACGCCTGGCAGAGGACCCTGCCGAGCCCAGGTACCGTGCCCGCCAGCGG
AGGGCCCGCTTTGTGTCCAAGAAAGGCAACTGCAACGTGGCCCACAAGAACATCCGGGAG
CAGGGCCGCTTCCTGCAGGACGTGTTCACCACGCTGGTGGACCTCAAGTGGCCACACACA
TTGCTCATCTTCACCATGTCCTTCCTGTGCAGCTGGCTGCTCTTCGCCATGGCCTGGTGG
CTCATCGCCTTCGCCCACGGTGACCTGGCCCCCAGCGAGGGCACTGCTGAGCCCTGTGTC
ACCAGCATCCACTCCTTCTCGTCTGCCTTCCTTTTCTCCATTGAGGTCCAAGTGACTATT
GGCTTTGGGGGGCGCATGGTGACTGAGGAGTGCCCACTGGCCATCCTGATCCTCATCGTG
CAGAACATCGTGGGGCTCATGATCAACGCCATCATGCTTGGCTGCATCTTCATGAAGACT
GCCCAAGCCCACCGCAGGGCTGAGACCCTCATCTTCAGCAAGCATGCGGTGATCGCCCTG
CGCCACGGCCGCCTCTGCTTCATGCTACGTGTGGGTGACCTCCGCAAGAGCATGATCATC
AGCGCCACCATCCACATGCAGGTGGTACGCAAGACCACCAGCCCCGAGGGCGAGGTGGTG
CCCCTCCACCAGGTGGACATCCCCATGGAGAACGGCGTGGGTGGCAACAGCATCTTCCTG
GTGGCCCCGCTGATCATCTACCATGTCATTGATGCCAACAGCCCACTCTACGACCTGGCA
CCCAGCGACCTGCACCACCACCAGGACCTCGAGATCATCGTCATCCTGGAAGGCGTGGTG
GAAACCACGGGCATCACCACCCAGGCCCGCACCTCCTACCTGGCCGATGAGATCCTGTGG
GGCCAGCGCTTTGTGCCCATTGTAGCTGAGGAGGACGGACGTTACTCTGTGGACTACTCC
AAGTTTGGCAACACCATCAAAGTGCCCACACCACTCTGCACGGCCCGCCAGCTTGATGAG
GACCACAGCCTACTGGAAGCTCTGACCCTCGCCTCAGCCCGCGGGCCCCTGCGCAAGCGC
AGCGTGCCCATGGCCAAGGCCAAGCCCAAGTTCAGCATCTCTCCAGATTCCCTGTCCTGA
GCCATGGTCTCTCGGGCCCCCCACACGCGTGTGTACACACGGACCATGTGGTATGTAGCC
CAGCCAGGGCCTGGTGTGAGGCTGGGCCAGCCTCAGCTCAGCCTCCCCCTGCTGCTCATC
CAGGGTGTTACAAGGCACTTGTCACTATGCTATTTCTGGCCTCAGCAGGAACCTGTACTG
GGTTATTTTTGTCCCTGCTCCTCCCAACCCAATTTAGGACTGGCTCACCCCTCTCCCCCG
CCCAAGGCTGCAGAGGCTGTGGGAGGTACTGGGCCCTAGAGCTGTGCGTCCAGCCAGTCC
TGGGTCCCCACGATTGACCAGCCACACTCTGGGCCGGTGGCTGGGGAAGAACAATCCCCG
AGGGCTGCTGCTTTGCGTCTGTGGCTCCAAGAAGTGCCTGTGGTCAGGCCCCAGCTCTAC
TTGGTCCCTGAAAAAGCACCCGGCTAAGGGCTGGGCCTGGCCAGCAGGGAGGGCAGTTGA
TGAGAGAGGGTGTTCCCGCTGGAGGGTTGGTGCTGTGGAGCCTACACCGGCAGGGACAGC
CTGGGGCTGACAGGGCTCCCCTCCGAGGGCCAGTTTCAGGTCTGGAAGGGGAGGAAGCAG
GGGAAGGTGACCTGAGGAGGCTCGGCTTTGTAGAGCCCCGCTCAGGCACAGGGAGGAGGA
GATGCCAGGGCTCCTGCCTTTTGCCACATCGGCCTCGTGCAGTGAGGGCTCTGTGGGCTG
GGGCTGCTGCCCCTGCCTACCTCCTGCCTGTCCCCAGAGGCTGAGGAGAGGGGGTACTGT
GCCCACCACACATGATTAGGCCTCAGACCCAACTCTGGTCCTGGCTCCACAACAGTGGCT
GCCACTCACTTTGTCCAGAAGGTGGCTTGGGGGTGGATATCTTTGGGTTGCTGGAAAAGG
TGTGGGAAGGTTCAGGATGGTGGGAGGGACTGAGGTCCCTGAGGTGAAGAGGCCCTTGGT
CCTGACGGGTTTGACCCGTGCCTGGACCCTTGGAGCAGTGTTGTGTGAACTTGCCTAGAA
CTCTGCCTTCTCCGTTGTCAATAAAGCCTCCCCCTCATGAAAAAAAAAAAAAAAAAA
Restriction Sites Please inquire     
ACCN NM_000525
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
OTI Annotation This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.
Product Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_000525.3, NP_000516.3
RefSeq Size 3418 bp
RefSeq ORF 1173 bp
Locus ID 3767
Cytogenetics 11p15.1
Protein Families Druggable Genome, Ion Channels: Potassium, Transmembrane
Protein Pathways Type II diabetes mellitus
Gene 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]'
Transcript Variant: This variant (1) encodes the longer protein (isoform 1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The extent of this transcript is supported by transcript alignments.

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