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GABA A Receptor beta 3 (GABRB3) (NM_000814) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201993L2V
- LentiORF®
-
Lenti ORF particles, GABRB3 (mGFP-tagged) - Human gamma-aminobutyric acid (GABA) A receptor, beta 3 (GABRB3), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
| Product Data | |
| Product Name | GABA A Receptor beta 3 (GABRB3) (NM_000814) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | DEE43; ECA5; EIEE43 |
| Vector | pLenti-C-mGFP |
| ACCN | NM_000814 |
| ORF Size | 1419 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201993).
|
| 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_000814.4 |
| RefSeq Size | 5811 bp |
| RefSeq ORF | 1422 bp |
| Locus ID | 2562 |
| Domains | Neur_chan_memb, Neur_chan_LBD |
| Protein Families | Druggable Genome, Ion Channels: Cys-loop Receptors, Transmembrane |
| Protein Pathways | Neuroactive ligand-receptor interaction |
| MW | 54.1 kDa |
| Gene Summary | This gene encodes a member of the ligand-gated ionic channel family. The encoded protein is one the subunits of a multi-subunit chloride channel that serves as the receptor for gamma-aminobutyric acid, a major inhibitory neurotransmitter of the mammalian nervous system. This gene is located on the long arm of chromosome 15 in a cluster with two other genes encoding related subunits of the family. This gene may be associated with the pathogenesis of several disorders including Angelman syndrome, Prader-Willi syndrome, nonsyndromic orofacial clefts, epilepsy and autism. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013] |
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