Kcnip2 (NM_145704) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR223584L4V
- LentiORF®
Lenti ORF particles, Kcnip2 (GFP-tagged) - Mouse Kv channel-interacting protein 2 (Kcnip2), transcript variant c, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Mouse Tagged ORF Clone |
Tag | mGFP |
Symbol | Kcnip2 |
Synonyms | KChI; KChIP2 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_145704 |
ORF Size | 660 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR223584).
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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_145704.1, NP_663750.1 |
RefSeq Size | 663 bp |
RefSeq ORF | 663 bp |
Locus ID | 80906 |
UniProt ID | Q9JJ69 |
Cytogenetics | 19 38.75 cM |
Gene Summary | This gene encodes a member of the voltage-gated potassium channel-interacting protein (KCNIP) family. KCNIP family members are small calcium binding proteins that commonly exhibit unique variation at their N-termini, and which modulate A-type potassium channels. This gene is predominantly expressed in the adult heart, and to a lesser extent in the brain. Disruption of this gene is associated with susceptibility to cardiac arrhythmias and lack of transient outward potassium current in ventricular myocytes, and downregulated expression is associated with cardiac hypertrophy. The encoded protein has also been implicated as a repressor of immune response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013] |
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