EAAT2 (SLC1A2) (NM_001195728) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC230852L3V
- LentiORF®
Lenti ORF particles, SLC1A2 (Myc-DDK-tagged)-Human solute carrier family 1 (glial high affinity glutamate transporter), member 2 (SLC1A2), transcript variant 2, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK mGFP mGFP w/ Puro
Product Images
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | EAAT2 |
Synonyms | DEE41; EAAT2; EIEE41; GLT-1; HBGT |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001195728 |
ORF Size | 1722 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC230852).
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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_001195728.2, NP_001182657.1 |
RefSeq Size | 11659 bp |
RefSeq ORF | 1698 bp |
Locus ID | 6506 |
UniProt ID | P43004 |
Cytogenetics | 11p13 |
Protein Families | Transmembrane |
Protein Pathways | Amyotrophic lateral sclerosis (ALS) |
MW | 62.1 kDa |
Gene Summary | This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Improper regulation of this gene is thought to be associated with several neurological disorders. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2017] |
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