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ADAM23 Recombinant Rabbit mAb (SDT-3115-27)

ADAM23 Recombinant Rabbit mAb (SDT-3115-27)

Catalog Number: S0B3682 Application: Sandwich ELISA Reactivity: Hu Conjugation: Unconjugated Brand: Starter
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Regular price $1,170 USD
Regular price Sale price $1,170 USD
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Product Details

Product Specification


Host Rabbit
Antigen ADAM23
Synonyms Metalloproteinase-like, disintegrin-like, and cysteine-rich protein 3 (MDC-3)
Accession O75077
Clone Number SDT-3115-27
Antibody Type Recombinant mAb
Isotype IgG
Application Sandwich ELISA
Reactivity Hu
Predicted Reactivity Ms
Cross Reactivity

No cross-reactivity against ADAM22

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

PBS pH7.4, 0.03% Proclin 300

Stability & Storage

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

Background

ADAM23 is a member of the ADAM (A Disintegrin and Metalloproteinase) family of transmembrane proteins. Unlike many ADAMs, it is considered a "silent" or non-proteolytic member because its metalloproteinase domain is catalytically inactive due to key mutations. Its primary biological function stems from its disintegrin and extracellular domains, which mediate cell-cell and cell-matrix interactions by binding to integrins and other surface proteins, particularly within the nervous system.Biologically, ADAM23 is predominantly expressed in the brain and is crucial for neuronal development and synaptic function. It interacts with proteins like LGI1 (leucine-rich glioma-inactivated 1) to regulate synaptic transmission and neuronal excitability. Mutations in the ADAM23 gene have been linked to inherited epileptic disorders, highlighting its role in maintaining normal brain circuitry.The significance of ADAM23 extends to oncology, where it is frequently identified as a tumor suppressor. Its expression is often downregulated or silenced via promoter hypermethylation in various cancers, including glioblastoma, breast, and lung carcinomas. This loss is associated with increased tumor progression, metastasis, and poor patient prognosis. The protein's adhesive functions are believed to suppress malignancy by promoting stable cellular interactions and inhibiting migration. Furthermore, research suggests ADAM23 may influence signaling pathways that control cell proliferation and survival. Its role as a diagnostic or prognostic biomarker is being investigated, and understanding its precise mechanisms could inform novel therapeutic strategies for both neurological diseases and cancer, making it a protein of considerable translational interest.

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