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KCTD7


Official Full Name
potassium channel tetramerization domain containing 7
Organism
Homo sapiens
Gene ID
154881
Background
This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]
Synonyms
EPM3; CLN14

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SHH324043 shRNA set against Mouse KCTD7 (NM_172509.3) Inquiry
SHH324039 shRNA set against Human KCTD7 (NM_153033.4) Inquiry
SHL193440 shRNA set against Mouse Kctd7(NM_172509.3) Inquiry
SHW002275 shRNA set against Chicken KCTD7 (NM_001039269) Inquiry
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OE-PNDC000377 Human KCTD7 Nanodisc Inquiry
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MiUTR1M-06287 KCTD7 miRNA 3'UTR clone Inquiry
MiUTR4H-TG04739 KCTD7 miRNA 3'UTR clone Inquiry
CDCB163750 Chicken KCTD7 ORF Clone (NM_001039269) Inquiry
CDCB171677 Danio rerio KCTD7 ORF Clone (NM_001045333) Inquiry
CDCB190654 Rabbit KCTD7 ORF clone (XM_002722279.2) Inquiry
CDCR271116 Mouse Kctd7 ORF Clone(NM_172509.3) Inquiry
CDCR376716 Rat Kctd7 ORF Clone(NM_001128194.2) Inquiry
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