mProX™ Human GRIN1/GRIN2A Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Ion Channel Cell Lines
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Published Data
Fig.1 Subcellular distribution of GRIN1 and Goα.
Following SDS-PAGE resolution, subcellular fractions were immunoblotted using the designated antibodies. COS cells that were transfected to express Goα and GRIN1.There are five lanes: one for untransfected COS cells (1000 × g supernatant); another for transfected COS cells (1000 × g supernatant); a fourth for transfected cells (10,000 × g supernatant); and a fifth for transfected cells (100,000 × g pellet).
Ref: Chen, Linda T., Alfred G. Gilman, and Tohru Kozasa. "A candidate target for G protein action in brain." Journal of Biological Chemistry 274.38 (1999): 26931-26938.
Pubmed: 10480904
DOI: 10.1074/jbc.274.38.26931
Research Highlights
Changes in the N-methyl-d-aspartate receptor (NMDAR) component GluN2A, which is encoded by GRIN2A, have been linked to a variety of neurodevelopmental diseases, including epilepsy and illnesses with strong speech-related symptoms.
Strehlow, Vincent, et al. "GRIN2A-related disorders: genotype and functional consequence predict phenotype." Brain 142.1 (2019): 80-92.
Pubmed:
30544257
DOI:
10.1093/brain/awy304
Research employing a diverse range of techniques, including molecular cytogenetics, next-generation sequencing technologies, and functional assays, has enabled the detection and confirmation of genetic mutations in the GRIN2A gene that may be directly responsible for a number of EAS illnesses.
Lesca, Gaetan, et al. "Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations." Epileptic Disorders 21 (2019): S41-S47.
Pubmed:
31149903
DOI:
10.1684/epd.2019.1056