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GAP43 Recombinant Rabbit mAb (SDT-3733-16)

GAP43 Recombinant Rabbit mAb (SDT-3733-16)

Catalog Number: S0B3775 Application: Sandwich ELISA Reactivity: Hu Conjugation: Unconjugated Brand: Starter
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Product Details

Product Specification


Host Rabbit
Antigen GAP43
Synonyms Neuromodulin; Axonal membrane protein GAP-43; Growth-associated protein 43; Neural phosphoprotein B-50; pp46; GAP43
Immunogen Recombinant Protein
Accession P17677
Clone Number SDT-3733-16
Antibody Type Recombinant mAb
Isotype IgG
Application Sandwich ELISA
Reactivity Hu
Predicted Reactivity Ms, Rt
Cross Reactivity

No cross reactivity against GFAP

Purification Protein A
Concentration 2mg/ml
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS pH7.4, 0.09% sodium azide

Stability & Storage

12 months from date of receipt, 2 to 8 °C as supplied

Background

GAP43 protein, also known as growth-associated protein 43, is a crucial molecule in the nervous system. It is predominantly expressed in neurons and plays a vital role in axonal growth and regeneration. During the development of the nervous system, GAP43 is highly expressed in growth cones at the tips of growing axons, where it helps to mediate the interactions between the axon and its surrounding environment, guiding the direction of axonal extension. In the adult nervous system, its expression can be upregulated in response to injury, facilitating the repair and reconnection of damaged neural circuits. Additionally, GAP43 is involved in synaptic plasticity, contributing to the strengthening and remodeling of synapses, which is essential for learning and memory processes. Its phosphorylation and dephosphorylation states can regulate its function, and alterations in GAP43 levels or activity have been implicated in various neurological disorders, making it an important target for research in neuroregeneration and neurodegenerative diseases.

For IVD, elevated CSF or plasma GAP-43 reflects impaired synapses and correlates with tau pathology in Alzheimer’s disease, helping identify at-risk mild cognitive impairment patients and predict cognitive decline. It also indicates axonal regeneration after neural injury and altered plasticity in epilepsy and neuropsychiatric disorders. Its measurement supports early differential diagnosis, disease staging, and therapeutic monitoring in neurodegeneration, complementing established AD biomarkers for synaptic loss evaluation.

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