{"product_id":"oma1-antibody-overlapping-with-the-m-aaa-protease-1-bha17135355","title":"OMA1 Antibody \/ Overlapping with the m-AAA protease 1","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eOMA1 Antibody \/ Overlapping with the m-AAA protease 1 is a anti-OMA1 Rabbit antibody Polyclonal (rabbit origin) supplied in Lyophilized format. Recommended for workflows such as Western blot (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), Immunofluorescence (IF), Flow cytometry (FACS), ELISA with listed reactivity in Human, Mouse, Rat. Reported localization: Mitochondria in cytoplasm, nucleus.\u003c\/p\u003e\u003ch2\u003eKey elements and design rationale\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eTarget:\u003c\/strong\u003e OMA1\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eAntibody details:\u003c\/strong\u003e Rabbit, Polyclonal (rabbit origin), isotype Rabbit IgG\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormat:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eApplications (as listed):\u003c\/strong\u003e WB, IHC, ICC\/IF, FACS, ELISA\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eBiological background\u003c\/h2\u003e\u003cdiv\u003eOMA1 antibody recognizes Metallopeptidase OMA1, a zinc-dependent mitochondrial protease that plays a critical role in regulating mitochondrial dynamics and quality control. OMA1 cleaves OPA1, an inner mitochondrial membrane GTPase, under stress conditions such as loss of membrane potential or proteotoxic stress. This cleavage promotes mitochondrial fission, facilitating the removal of damaged mitochondria through mitophagy. The OMA1 antibody is widely used in research on mitochondrial homeostasis, apoptosis, and neurodegenerative disease mechanisms that involve disrupted mitochondrial morphology.\u003cbr\u003e\u003cbr\u003eOMA1 is encoded by the OMA1 gene located on human chromosome 1p32.2. It encodes an integral membrane protein of the inner mitochondrial membrane, with its catalytic domain facing the intermembrane space. The protein contains a conserved HEXXH metalloprotease motif required for zinc ion coordination and proteolytic activity. OMA1 exists in inactive and active forms that are regulated by mitochondrial potential and proteolytic turnover. Activation leads to processing of long isoforms of OPA1 into short forms, promoting mitochondrial fragmentation during stress.\u003cbr\u003e\u003cbr\u003eThe OMA1 antibody is valuable for investigating mitochondrial stress pathways and proteolytic processing events. Western blot analysis typically detects bands near 60-65 kDa, corresponding to the precursor and active forms of OMA1. In immunocytochemistry, the antibody reveals punctate mitochondrial staining, confirming localization within the inner membrane network. Functional studies using OMA1-deficient cells demonstrate its essential role in maintaining mitochondrial morphology and preventing accumulation of dysfunctional organelles. Loss of OMA1 activity has been associated with neurodegeneration, cardiomyopathy, and metabolic syndromes due to impaired mitochondrial adaptation.\u003cbr\u003e\u003cbr\u003eOMA1 acts in concert with other mitochondrial proteases, including YME1L1 and PARL, to fine-tune the balance between fusion and fission events. It also participates in the mitochondrial unfolded protein response and contributes to stress-induced apoptosis.\u003c\/div\u003e\u003ch2\u003eResearch relevance and current trends\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eConnecting protein-level changes to phenotype using orthogonal readouts (genetic perturbation, transcriptomics, imaging).\u003c\/li\u003e\n\u003cli\u003eConsidering isoforms and post-translational regulation when interpreting protein-level changes.\u003c\/li\u003e\n\u003cli\u003eComparing results across species and model systems with matched controls.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eCommon research applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eWestern blotting:\u003c\/strong\u003e compare relative abundance and activation-state changes across conditions.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eImmunofluorescence:\u003c\/strong\u003e visualize subcellular distribution and cell-to-cell heterogeneity.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eImmunohistochemistry:\u003c\/strong\u003e map target signal in tissue context and compare regions\/phenotypes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFlow cytometry:\u003c\/strong\u003e quantify target-positive populations and signal shifts at single-cell resolution.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eELISA:\u003c\/strong\u003e support antibody-based quantification in assay formats where applicable.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eInterpret changes in signal alongside appropriate controls and, when relevant, in parallel with total-protein or pathway readouts.\u003c\/p\u003e\u003ch2\u003eNotes for experimental interpretation\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eSignal can reflect expression level, isoform composition, and post-translational state; interpret results in the context of your model system and stimuli.\u003c\/li\u003e\n\u003cli\u003eSpecies differences and sample matrices can influence epitope recognition; prioritize matched controls and orthogonal confirmation when feasible.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eAntibody notes:\u003c\/strong\u003e Polyclonal antibodies recognize multiple epitopes, which can broaden the epitope footprint and may increase sensitivity in some contexts.\u003c\/p\u003e\u003c!-- Sources (internal): - UniProt search — UniProt — https:\/\/www.uniprot.org\/uniprotkb?query=OMA1 - NCBI Gene search — NCBI — https:\/\/www.ncbi.nlm.nih.gov\/gene\/?term=OMA1 - Ensembl search — Ensembl — https:\/\/www.ensembl.org\/Multi\/Search\/Results?q=OMA1 - Human Protein Atlas search — HPA — https:\/\/www.proteinatlas.org\/search\/OMA1 - PubMed (review) — NLM — https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=OMA1+review --\u003e","brand":"NSJ Bioreagents","offers":[{"title":"Adding 0.2 ml of distilled water will yield a concentration of 500 ug\/ml \/ 100 ug","offer_id":53047289086317,"sku":"FY12452","price":449.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/get_image_d319eabf-6265-4e69-9f82-e015afaf739c.jpg?v=1782237008","url":"https:\/\/www.ebiohippo.com\/products\/oma1-antibody-overlapping-with-the-m-aaa-protease-1-bha17135355","provider":"BioHippo","version":"1.0","type":"link"}