Anti-GluN1 Antibody [N308/48]

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SKU:
STMA00124
Antibody Type:
Monoclonal
Applications:
WB
Applications:
IHC
Applications:
ICC/IF
Reactivity:
Human
Reactivity:
Mouse
Reactivity:
Rat
Host Species:
Mouse
Isotype:
IgG1
  • Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-GluN1 Monoclonal Antibody, Clone N308/48 (STMA00124). Tissue: Neuroblastoma cells (SH-SY5Y). Species: Human. Fixation: 4% PFA for 15 min. Primary Antibody: Mouse Anti-GluN1 Monoclonal Antibody (STMA00124) at 1:50 for overnight at 4°C with slow rocking. Secondary Antibody: AlexaFluor 488 at 1:1000 for 1 hour at RT.
  • Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-GluN1 Monoclonal Antibody, Clone N308/48 (STMA00124). Tissue: Neuroblastoma cell line (SK-N-BE). Species: Human. Fixation: 4% Formaldehyde for 15 min at RT. Primary Antibody: Mouse Anti-GluN1 Monoclonal Antibody (STMA00124) at 1:100 for 60 min at RT. Secondary Antibody: Goat Anti-Mouse ATTO 488 at 1:100 for 60 min at RT.
  • Western Blot analysis of Rat brain membrane lysate showing detection of GluN1 protein using Mouse Anti-GluN1 Monoclonal Antibody, Clone N308/48 (STMA00124). Primary Antibody: Mouse Anti-GluN1 Monoclonal Antibody (STMA00124) at 1:1000.
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Description

GluN1 Antibody [N308/48]

GluN1 Antibody [N308/48] is a mouse monoclonal antibody directed against GluN1, offered by Assay Genie for research applications. Reported applications include WB, IHC and ICC/IF. Reported reactivity: Human, Mouse and Rat. Supplied as IgG1, purified by Protein G.

The N-methyl-D-aspartate receptor (NMDA receptor or NMDAR) is a glutamate-gated ion channel essential for synaptic plasticity, learning, and memory. Central to its function is the GluN1 subunit, encoded by the GRIN1 gene, which is an obligatory component of all functional NMDAR complexes. Each receptor is a heterotetramer typically composed of two GluN1 subunits and two regionally expressed GluN2 (A-D) subunits. The GluN1 subunit not only anchors the receptor’s core structure but also modulates its biophysical and pharmacological properties through alternative splicing, generating multiple isoforms with distinct functional profiles. GluN1’s ubiquitous expression and essential role in receptor assembly make it a focal point in neuroscience and neurodegenerative disease research. Dysregulation of GluN1 expression or splicing has been implicated in a range of neurological disorders, including Alzheimer’s disease, Huntington’s disease, and schizophrenia. Additionally, GluN3 subunits (A and B), which can co-assemble with GluN1, exert inhibitory effects on receptor activity, further influencing disease-relevant signaling pathways. Understanding GluN1’s molecular diversity and regulatory mechanisms is critical for developing targeted therapies aimed at restoring NMDAR function in neurodegenerative and neuropsychiatric conditions. This antibody is also available conjugated to ATTO 390, ATTO 488, ATTO 594, APC, Biotin, FITC, HRP, PerCP and RPE. Supplied in 100 µg. For research use only; not for diagnostic or therapeutic procedures.

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