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SMC-394

VGLUT1 Antibody, Clone N28/9

Eine Lieferung in diese Region ist nicht möglich.

SKU:
SMC-394
Zusätzliche Namen:
VGLUT1, Vesicular Glutamate Transporter 1, SLC17A7, BNPI, Solute Carrier Family 17 Member 7, Brain-specific Na(+)-dependent Inorganic Phosphate Cotransporter, Solute Carrier Family 17 (Sodium-Dependent Inorganic Phosphate Cotransporter), Member 7, Solute Carrier Family 17 (Vesicular Glutamate Transporter), Member 7, VGluT1, VGLUT 1
Anwendung:
IHC, WB
Konzentration:
1 mg/ml
Spezies-Reaktivität:
Rat
Aufreinigung:
Protein G Purified
Lagerbedingungen:
-20[o]C
Hersteller:
StressMarq Biosciences
Host:
Mouse
Reaktivitäten:
Human, Mouse, Rat
ABP:
IMP-GEN-2015-06 < 10% Serum <100ml
Buffer:
PBS pH7.4, 50% glycerol, 0.09% sodium azide
Immunogen:
Fusion protein amino acids 493-560 (cytoplasmic C-terminus) of rat VGlut1
Klon:
N28/9 (Formerly sold as S28-9)
Uniprot:
Q62634
Synonyme:
BNPI;brain-specific Na-dependent inorganic phosphate cotransporter;brain-specific Na(+)-dependent inorganic phosphate cotransporter;solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7;solute carrier family 17 (vesicular glutamate transporter), member 7;Solute carrier family 17 member 7;vesicular glutamate transporter 1;Vglut1
Weitere Details:
Vesicular glutamate transporter 1 (VGLUT1) plays a critical role in glutamatergic neurotransmission by packaging glutamate into synaptic vesicles for release at excitatory synapses. Expressed in a specific subset of glutamatergic neurons, VGLUT1 exhibits a unique chloride conductance that is inhibited by glutamate, highlighting its dual role in vesicle loading and ion homeostasis. Unlike high-affinity plasma membrane excitatory amino acid transporters (EAATs), VGLUT1 operates with a lower apparent affinity, with a Km of approximately 2 mM-comparable to native synaptic vesicle transport kinetics. Importantly, VGLUT1 demonstrates substrate specificity by selectively transporting glutamate, but not aspartate, distinguishing it from EAATs that recognize both. This specificity underscores VGLUT1's essential function in maintaining synaptic fidelity and excitatory signaling precision. Emerging evidence links dysregulation of VGLUT1 expression and function to several neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS). Altered glutamate homeostasis, driven by impaired vesicular transport, contributes to excitotoxicity-a key pathological mechanism in these conditions. As a result, VGLUT1 has become a focal point in neuroscience and neurodegenerative disease research, offering potential as both a biomarker and a therapeutic target. Understanding its molecular properties and regulatory mechanisms is essential for developing strategies to modulate glutamatergic signaling in disease contexts.
Versandbedingungen:
Blue Ice