Hamartin Antibody

SKU:BHA17101501
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NSJ Bioreagents
NSJ Bioreagents
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    Overview
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    Anti-Hamartin polyclonal antibody (Rabbit Ig) for target detection, validation, and assay development. Reactivity: Human; antigen-affinity purified reagent to support WB, IHC, IF, and ELISA.
    Target Hamartin
    Host Rabbit
    Isotype Rabbit Ig
    Reactivity Human
    Application(s) WB, IHC, IF, ELISA
    Available Options

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

    • Options (Formulation: In 1X PBS, pH 7.4, with 0.09% sodium azide; Size (2) — 0.08 ml, 0.4 ml)
    • Lead time: options listed as “In Stock at Manufacturer” typically ship after a short processing time (2–3 days). Timing may vary by fulfillment source.
    • Storage: Refer to the product datasheet for storage and handling.
    • Shipping: cold-chain shipment (typically with ice packs).
    • Upon receipt: follow the product datasheet storage instructions.
    • Sales terms and conditions: Please review prior to ordering.
    Options selector
    Catalog no. Formulation Size
    F49609-0.08ML In 1X PBS, pH 7.4, with 0.09% sodium azide
    Field Specification
    Clonality
    • Polyclonal (rabbit origin)
    Host Rabbit
    Immunogen A portion of amino acids 401-430 from the human protein was used as the immunogen for this Hamartin antibody.
    Isotype
    • Rabbit Ig
    Product Type
    • Antibodies
    • Primary Antibodies
    Purity Antigen affinity
    Reactivity
    • Human
    Storage Aliquot the Hamartin antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
    Target Hamartin
    UniProt # Q92574

    Implicated as a tumor suppressor. May have a function in vesicular transport. Interaction between TSC1 and TSC2 may facilitate vesicular docking. Defects in TSC1 are the cause of tuberous sclerosis complex (TSC). The molecular basis of TSC is a functional impairement of the hamartin-tuberin complex. TSC is an autosomal dominant multi-system disorder that affects especially the brain, kidneys, heart, and skin. TSC is characterized by hamartomas (benign overgrowths predominantly of a cell or tissue type that occurs normally in the organ) and hamartias (developmental abnormalities of tissue combination). Clinical symptoms can range from benign hypopigmented macules of the skin to profound mental retardation with intractable seizures to premature death from a variety of disease-associated causes. Defects in TSC1 may be a cause of focal cortical dysplasia of Taylor balloon cell type (FCDBC). FCDBC is a subtype of cortical displasias linked to chronic intractable epilepsy. Cortical dysplasias display a broad spectrum of structural changes, which appear to result from changes in proliferation, migration, differentiation, and apoptosis of neuronal precursors and neurons during cortical development.

    • Format: Antigen affinity purified

    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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