Kir7.1 (KCNJ13) (NM_001172417) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC229820L4V

  • LentiORF®

Lenti ORF particles, KCNJ13 (mGFP-tagged)-Human potassium inwardly-rectifying channel, subfamily J, member 13 (KCNJ13), transcript variant 3, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 880.00

11 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol KCNJ13
Synonyms KIR1.4; KIR7.1; LCA16; SVD
Mammalian Cell Selection Puromycin
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_001172417
ORF Size 840 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC229820).
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_001172417.1, NP_001165888.1
RefSeq Size 3376 bp
RefSeq ORF 843 bp
Locus ID 3769
UniProt ID O60928
Cytogenetics 2q37.1
Protein Families Druggable Genome, Ion Channels: Potassium, Transmembrane
MW 31.1 kDa
Gene Summary This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]

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