Trim25 Antibody / Efp

SKU:BHA17110978
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NSJ Bioreagents
NSJ Bioreagents
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    Overview
    Click light‑blue chips for details
    Research-use anti-EFP primary antibody (Rabbit, isotype Rabbit IgG) for WB, IHC-P, IF, FACS and related target-detection assays in RUO workflows.
    Target EFP
    Host Rabbit
    Reactivity Mouse, Rat
    Conjugate(s) Unconjugated
    Application WB, IHC-P, IF, FACS, Direct ELISA
    Options selector
    Catalog no. Formulation Size
    RQ6343 0.5mg/ml if reconstituted with 0.2ml sterile DI water
    Available Options

    Select the variant that best fits your experiment. Availability and lead time may vary by option.

    • Options: Formulation: 0.5mg/ml if reconstituted with 0.2ml sterile DI water; Size: 100 ug
    • Lead time: typically ships in ~2–3 business days; timing may vary by selected option.
    • Storage: After reconstitution, the Trim25 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
    • Shipping: cold-chain shipment (typically with ice packs).
    • Upon receipt: store at the recommended temperature as soon as possible.
    • Sales terms and conditions: Please review prior to ordering.
    Field Specification
    Clonality
    • Polyclonal (rabbit origin)
    Host Rabbit
    Immunogen Recombinant mouse protein (amino acids M1-H590) was used as the immunogen for the Trim25 antibody.
    Isotype
    • Rabbit IgG
    Product Type
    • Antibodies
    • Primary Antibodies
    Purity Antigen affinity purified
    Reactivity
    • Mouse
    • Rat
    Storage After reconstitution, the Trim25 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
    Target EFP
    UniProt # Q61510

    Overview

    Trim25 Antibody / Efp is a research-use primary antibody intended for detection of EFP in experimental workflows. It is supplied in Purified format. Key antibody attributes include Rabbit, Polyclonal (rabbit origin), isotype Rabbit IgG. Applications listed for this product include WB, IHC-P, IF, FACS, Direct ELISA. Reported/annotated localization context: Nuclear, cytoplasmic. Species reactivity (as provided): Mouse, Rat.

    Key elements and design rationale

    • Target: EFP (Trim25) — selectivity and interpretation should be considered in the context of isoforms, post-translational modifications, and related family members when applicable.
    • Format: Purified — format can influence background, multiplexing compatibility, and downstream detection strategies.
    • Antibody identity: Rabbit, Polyclonal (rabbit origin), isotype Rabbit IgG — these attributes help align secondary reagents and controls (e.g., isotype-matched controls) with your assay design.
    • Localization: Nuclear, cytoplasmic — expected subcellular distribution can guide band/structure interpretation and help flag off-target signal.
    • Product notes (from provided description): Tripartite motif-containing protein 25 is a protein that in humans is encoded by the TRIM25 gene. It is mapped to 17q22. The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. The presence of potential DNA-binding and dimerization-transactivation domains suggests that this protein may act as a transcription factor, similar to several other members of the TRIM family. Expression of the gene is upregulated in response to estrogen, and it is thought to mediate estrogen actions in breast cancer as a primary response gene.

    Where multiple assay formats are possible, align the antibody format, host/isotype, and listed applications with your detection system and controls to support clear interpretation of signal.

    Biological background

    In this catalog, EFP is positioned within Molecular & Cellular Biology, Cancer research contexts. Localization annotations (e.g., Nuclear, cytoplasmic) can help contextualize expected signal patterns in imaging and fractionation-based readouts. For authoritative gene/protein nomenclature, domains/isoforms, and curated functional annotations, consult resources such as UniProt, NCBI Gene, and Ensembl.

    Research relevance and current trends

    • Higher-plex and spatially resolved readouts (e.g., multiplex IF/IHC, spatial omics) are increasing demand for well-characterized primary antibodies with clearly stated host/isotype and labeling strategies.
    • Genetic perturbation controls (knockout/knockdown) and orthogonal measurements (e.g., RNA vs protein) are commonly used to strengthen target attribution when interpreting antibody-derived signals.
    • Reproducibility initiatives emphasize transparent reporting of antibody identity (clone, host, isotype) and experimental context to improve cross-study comparability.

    Common research applications

    • WB: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
    • IHC-P: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
    • IF: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
    • FACS: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
    • Direct ELISA: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
    • Typical workflow themes: Western blot validation, IHC on FFPE tissue, IF/ICC localization, Flow cytometry staining, ELISA binding assay, Specificity controls.
    • Workflow notes: Validate EFP by Western blot in cell/tissue lysates (include controls), Detect EFP by IHC in FFPE tissue sections (optimize antigen retrieval + dilution), Detect EFP localization by IF/ICC in cultured cells (optimize…

    When comparing conditions, consistent sample processing and appropriate negative/positive controls support interpretation of qualitative localization differences and quantitative abundance changes.

    Notes for experimental interpretation

    • Isoforms and post-translational modifications may shift apparent molecular weight or epitope accessibility, especially across cell states or treatments.
    • Species and tissue context can affect sequence conservation, expression level, and background binding; predicted reactivity should be verified in your sample.
    • Control concepts include isotype-matched controls, secondary-only controls (for indirect detection), and genetic/orthogonal controls (e.g., KO/KD, independent antibodies, or RNA measurements) when feasible.

    Monoclonal and polyclonal antibodies can differ in epitope recognition breadth and lot-to-lot characteristics; consider clonality and clone information (when provided) alongside your assay requirements. Conjugated formats may simplify detection but can change background and multiplexing behavior compared with unconjugated primaries.

    Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.

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