CACNG3 (NM_006539) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC207373L3V
- LentiORF®
Lenti ORF particles, CACNG3 (Myc-DDK-tagged)-Human calcium channel, voltage-dependent, gamma subunit 3 (CACNG3), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | CACNG3 |
Synonyms | Cacng2; calcium channel, voltage-dependent, gamma subunit 3; neuronal voltage-gated calcium channel gamma-3 subunit; voltage-dependent calcium channel gamma-3 subunit; voltage-gated calcium channel gamma subunit |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_006539 |
ORF Size | 945 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC207373).
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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_006539.2, NP_006530.1 |
RefSeq Size | 2710 |
RefSeq ORF | 948 |
Locus ID | 10368 |
Domains | PMP22_Claudin |
Protein Families | Druggable Genome, Ion Channels: Other, Transmembrane |
Protein Pathways | Arrhythmogenic right ventricular cardiomyopathy (ARVC), Cardiac muscle contraction, Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM), MAPK signaling pathway |
MW | 35.5 kDa |
Gene Summary | The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family. This gene is a susceptibility locus for childhood absence epilepsy. [provided by RefSeq, Dec 2010] |
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