alpha 1 Glycine Receptor (GLRA1) (NM_000171) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC210390L1V
- LentiORF®
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Lenti ORF particles, GLRA1 (Myc-DDK tagged) - Human glycine receptor, alpha 1 (GLRA1), transcript variant 2, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | GLRA1 |
Synonyms | HKPX1; STHE |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_000171 |
ORF Size | 1347 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC210390).
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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_000171.1, NP_000162.1 |
RefSeq Size | 1811 bp |
RefSeq ORF | 1350 bp |
Locus ID | 2741 |
Cytogenetics | 5q33.1 |
Protein Families | Druggable Genome, Ion Channels: Cys-loop Receptors, Transmembrane |
Protein Pathways | Neuroactive ligand-receptor interaction |
MW | 51.7 kDa |
Gene Summary | 'The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found. [provided by RefSeq, Dec 2015]' |
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