Gene: GRID2
Official Full Name: glutamate ionotropic receptor delta type subunit 2provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans. [provided by RefSeq, Apr 2014]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA15601 | GRID2 Knockout cell line (AC16) | Human | GRID2 | 1:3-1:4 | negative | Online Inquiry |
| KOA31048 | GRID2 Knockout cell line (BEAS-2B) | Human | GRID2 | 1:3~1:4 | negative | Online Inquiry |
| KOA46469 | GRID2 Knockout cell line (U-2932) | Human | GRID2 | 1:2-1:4 | negative | Online Inquiry |
| KOA61861 | GRID2 Knockout cell line (TPC-1) | Human | GRID2 | 1:5-1:8 | negative | Online Inquiry |
| KOA77288 | GRID2 Knockout cell line (NCM460) | Human | GRID2 | 1:2~1:3 | negative | Online Inquiry |
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