{"product_id":"enolase-2-antibody-sc-f0885","title":"Enolase-2 Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eENOLASE-2 is a target of interest in many antibody-based workflows. Enolase is an enzyme found in the cytosol, playing a crucial role in glycolysis by converting 2-phosphoglycerate into phosphoenolpyruvate. It also serves as a moonlighting enzyme, associated with stress and hypoxic conditions, and in certain species, it's overexpressed in acidic environments. Enolase exists in three isoforms: ENO1 (composed of two α subunits), ENO2 (composed of two γ subunits), and ENO3 (composed of two β subunits). Depending on the literature source, ENOLASE-2 may also be discussed as Neuron Specific Enolase and NSE.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell membrane, cytoplasm, and membrane, which can matter when signal is compared across treatments or changing cell states. Following ENOLASE-2 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eENOLASE-2 is commonly interpreted in the context of neuroscience research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cell membrane, cytoplasm, and membrane, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cell membrane, cytoplasm, and membrane across matched conditions\u003c\/li\u003e\n\u003cli\u003ecompartment-specific patterns relevant to neuronal polarity, transport, or synaptic context\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for ENOLASE-2. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in ENOLASE-2 reflect biology rather than handling. When interpreting ENOLASE-2, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep ENOLASE-2 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577548808537,"sku":"F0885-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577548841305,"sku":"F0885-100UL","price":399.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577548874073,"sku":"F0885-2X100UL","price":599.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F0885-IHC1.jpg?v=1773599053","url":"https:\/\/absource-diagnostics.myshopify.com\/products\/enolase-2-antibody-sc-f0885","provider":"Absource Diagnostics","version":"1.0","type":"link"}