Recommended
product-img
  • Products
  • Discover MP Targets
  • Discover Research Areas
  • mProX™ Human GRIN1/GRIN2A Stable Cell Line

    [CAT#: S01YF-1123-KX70]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Ion Channel Cell Lines

    Datasheet MSDS Request COA

    Certificate of Analysis Lookup
    To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
    Lot Number

    Made to Order Inquiry

    Inquiry
    Host Cell Type:
    Membrane Protein Engineering:
    Fluorescent Marker:
    Resistance:
    Deliverable:

    Product Information

    Target Protein
    GRIN1/GRIN2A
    Target Family
    Glutamate Receptor
    Target Protein Species
    Human
    Host Cell Type
    COS-M6; CHO-K1; HEK293
    Target Classification
    Ion Channel Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Neurodevelopmental Disorder
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The human GRIN2A gene encodes the protein glutamate [NMDA] receptor subunit epsilon-1. The conventional GluN2A subunit isoform has a considerable length of 1464 amino acids. Alternative splicing can generate the monkey-specific GluN2A-short isoforms, which have 1281 amino acids. Ionotropic glutamate receptors include the N-methyl-D-aspartate (NMDA) receptor class. Long-term potentiation, an activity-dependent improvement in synaptic transmission efficiency believed to underpin some forms of memory and learning, has been linked to the NMDA channel. The main receptor subunit NMDAR1 (GRIN1) and one or more of the four NMDAR2 subunits-NMDAR2A (GRIN2A), NMDAR2B (GRIN2B), NMDAR2C (GRIN2C), and NMDAR2D (GRIN2D)-compose heteromers that make up NMDA receptor channels. The customized GRIN1/GRIN2A stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

    Protocols

    Please visit our protocols page.

    Customer Reviews

    There are currently no Customer reviews or questions for mProX™ Human GRIN1/GRIN2A Stable Cell Line (S01YF-1123-KX70). Click the button above to contact us or submit your feedback about this product.

    FAQ

    chat Sharon (Verified Customer)

    What host cells are typically used for the GRIN1/GRIN2A stable cell line? Aug 17 2020

    chat Sherry Smith (Creative Biolabs Scientific Support)

    Mammalian cells such as HEK293 or CHO-K1. Aug 17 2020

    chat Amy (Verified Customer)

    What is the BSL of the GRIN1/GRIN2A cell line? Dec 13 2022

    chat Sherry Smith (Creative Biolabs Scientific Support)

    The BSL of the GRIN1/GRIN2A cell line is Level 1. Dec 13 2022

    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

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
    Send Inquiry Send Inquiry
    Inquiry Basket
    compare

    Go to compare