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CACNB4 (NM_000726) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC210440L1V
- LentiORF®
-
Lenti ORF particles, CACNB4 (Myc-DDK tagged) - Human calcium channel, voltage-dependent, beta 4 subunit (CACNB4), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | CACNB4 (NM_000726) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CAB4; CACNLB4; EA5; EIG9; EJM; EJM4; EJM6 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_000726 |
| ORF Size | 1560 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC210440).
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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_000726.2 |
| RefSeq Size | 7979 bp |
| RefSeq ORF | 1563 bp |
| Locus ID | 785 |
| Domains | Ca_channel_B, SH3, GuKc |
| Protein Families | Druggable Genome, Ion Channels: Other |
| Protein Pathways | Arrhythmogenic right ventricular cardiomyopathy (ARVC), Cardiac muscle contraction, Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM), MAPK signaling pathway |
| MW | 58.2 kDa |
| Gene Summary | This gene encodes a member of the beta subunit family of voltage-dependent calcium channel complex proteins. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Various versions of each of these subunits exist, either expressed from similar genes or the result of alternative splicing. The protein encoded by this locus plays an important role in calcium channel function by modulating G protein inhibition, increasing peak calcium current, controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation. Certain mutations in this gene have been associated with idiopathic generalized epilepsy (IGE), juvenile myoclonic epilepsy (JME), and episodic ataxia, type 5. [provided by RefSeq, Aug 2016] |
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