KCNH7 (NM_173162) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC207714L4V

Lenti ORF particles, KCNH7 (mGFP-tagged)-Human potassium voltage-gated channel, subfamily H (eag-related), member 7 (KCNH7), transcript variant 2, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: KCNH7
• Synonyms: ERG3; HERG3; Kv11.3
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_173162
• ORF Size: 2196 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC207714).
• OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.

Reference Data

• RefSeq: NM_173162.1
• RefSeq Size: 2488 bp
• RefSeq ORF: 2199 bp
• Locus ID: 90134
• UniProt ID: Q9NS40
• Cytogenetics: 2q24.2
• Protein Families: Druggable Genome, ES Cell Differentiation/IPS, Ion Channels: Other, Transmembrane
• MW: 82.7 kDa
• Gene Summary: Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. There are at least two alternatively spliced transcript variants derived from this gene and encoding distinct isoforms. [provided by RefSeq, Jul 2008]