{"product_id":"cybb-antibody-sc-f1615","title":"NOX2\/gp91phox Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eCYBB is a target of interest in many antibody-based workflows. NOX2, also known as gp91phox, is a membrane-bound enzyme, the prototypical member of the NADPH oxidase NOX superfamily and produces superoxide (O2•−), a key reactive oxygen species (ROS) that is essential in innate and adaptive immunity. It serves as the catalytic core of the NADPH oxidase complex, predominantly found in phagocytic cells like neutrophils and macrophages. Depending on the literature source, CYBB may also be discussed as NOX2\/gp91phox and gp91-phox.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell membrane, which can matter when signal is compared across treatments or changing cell states. Following CYBB 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\u003eCYBB is commonly interpreted in the context of immunology, infectious disease, and oxidative stress research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cell 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\u003esignal enrichment within cell membrane relative to the broader cellular background\u003c\/li\u003e\n\u003cli\u003econtext differences tied to immune-cell state, activation, or lineage composition\u003c\/li\u003e\n\u003cli\u003ehost-response changes during infection or pathogen-associated stimulation\u003c\/li\u003e\n\u003cli\u003eredox-associated shifts that may alter abundance, localization, or pathway coupling\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 CYBB. 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 CYBB reflect biology rather than handling. When interpreting CYBB, 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 CYBB 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":57577795748185,"sku":"F1615-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577795780953,"sku":"F1615-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577795813721,"sku":"F1615-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1615-wb.gif?v=1773599941","url":"https:\/\/absource-diagnostics.myshopify.com\/products\/cybb-antibody-sc-f1615","provider":"Absource Diagnostics","version":"1.0","type":"link"}