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Mouse Anti-GRIN1 Monoclonal Antibody (54.1) (CBMAB-1422-YC)

Provided herein is a mouse monoclonal antibody against Human GRIN1. The antibody, clone 54.1, can be used for immunoassay techniques, such as IHC-P, IP, ELISA and WB.
See all GRIN1 antibodies
Published Data
Fig.1 NR1 is up-regulated in diabetic kidney and podocytes incubated in high glucose.
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Fig.2 NR1 is up-regulated in diabetic kidney and podocytes incubated in high glucose.
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Fig.3 NMDARs participate in DKD progression.
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Summary

Host Animal
Mouse
Specificity
Human, Rat, Hamster, Fish, Mouse
Clone
54.1
Antibody Isotype
IgG2a
Application
IHC-P, IP, ELISA, WB

Basic Information

Immunogen
Fusion protein containing sequence from the intracellular loop between transmembrane regions III and IV of NMDAR1.
Specificity
Human, Rat, Hamster, Fish, Mouse
Antibody Isotype
IgG2a
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Purity
>95%, as determined by SDS-PAGE analysis
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Glutamate Ionotropic Receptor NMDA Type Subunit 1
Introduction
GRIN1 is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. GRIN1 play a role in the plasticity of synapses, which is believed to underlie memory and learning.
Entrez Gene ID
Human2902
Mouse14810
Rat24408
Hamster100770880
UniProt ID
HumanQ05586
MouseP35438
RatP35439
HamsterA0A1U7R901
Alternative Names
NR1; MRD8; GluN1; NMDA1; NDHMSD; NDHMSR; NMD-R1; NMDAR1
Function
Component of NMDA receptor complexes that function as heterotetrameric, ligand-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Channel activation requires binding of the neurotransmitter glutamate to the epsilon subunit, glycine binding to the zeta subunit, plus membrane depolarization to eliminate channel inhibition by Mg2+ (PubMed:7685113, PubMed:28126851, PubMed:26919761, PubMed:26875626, PubMed:28105280).

Sensitivity to glutamate and channel kinetics depend on the subunit composition (PubMed:26919761).
Biological Process
Brain development Source: ARUK-UCL
Calcium ion homeostasis Source: UniProtKB
Calcium ion transmembrane import into cytosol Source: UniProtKB
Cation transport Source: UniProtKB
Chemical synaptic transmission Source: GO_Central
Excitatory chemical synaptic transmission Source: ARUK-UCL
Excitatory postsynaptic potential Source: UniProtKB
Ionotropic glutamate receptor signaling pathway Source: UniProtKB
Positive regulation of calcium ion transport into cytosol Source: ARUK-UCL
Positive regulation of cysteine-type endopeptidase activity Source: ARUK-UCL
Positive regulation of excitatory postsynaptic potential Source: BHF-UCL
Positive regulation of reactive oxygen species biosynthetic process Source: ARUK-UCL
Positive regulation of transcription by RNA polymerase II Source: UniProtKB
Propylene metabolic process Source: BHF-UCL
Protein heterotetramerization Source: UniProtKB
Regulation of membrane potential Source: UniProtKB
Regulation of synaptic plasticity Source: ARUK-UCL
Response to ethanol Source: UniProtKB
Response to glycine Source: UniProtKB
Visual learning Source: UniProtKB
Cellular Location
Cell membrane; Postsynaptic cell membrane; Postsynaptic density. Enriched in postsynaptic plasma membrane and postsynaptic densities.
Involvement in disease
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant (NDHMSD):
An autosomal dominant neurodevelopmental disorder characterized by severe mental retardation and developmental delay, absent speech, muscular hypotonia, dyskinesia, and hyperkinetic movements. Cortical blindness, cerebral atrophy, and seizures are present in some patients.
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive (NDHMSR):
An autosomal recessive neurodevelopmental disorder characterized by severe mental retardation and psychomotor developmental delay, involuntary and stereotypic movements, spasticity, and inability to walk without support. Intractable seizures manifest in some patients.
Topology
Extracellular: 19-559
Helical: 560-580
Cytoplasmic: 581-602
Discontinuously helical: 603-624
Cytoplasmic: 625-630
Helical: 631-647
Extracellular: 648-812
Helical: 813-833
Cytoplasmic: 834-938
PTM
NMDA is probably regulated by C-terminal phosphorylation of an isoform of NR1 by PKC. Dephosphorylated on Ser-897 probably by protein phosphatase 2A (PPP2CB). Its phosphorylated state is influenced by the formation of the NMDAR-PPP2CB complex and the NMDAR channel activity.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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