GPC3 Antibody

SKU:BHA17101497
Suppliers
NSJ Bioreagents
NSJ Bioreagents
Details Products
Overview
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Anti-GPC3 polyclonal antibody (Rabbit Ig) for target detection, validation, and assay development. Reactivity: Human, Mouse; purified reagent to support WB, IF, and ELISA.
Target GPC3
Host Rabbit
Isotype Rabbit Ig
Reactivity Human, Mouse
Application(s) WB, IF, ELISA
Options selector
Catalog no. Formulation Size
F49601-0.08ML In 1X PBS, pH 7.4, with 0.09% sodium azide
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.
Field Specification
Mfr No F49601
Clonality
  • Polyclonal (rabbit origin)
Host Rabbit
Immunogen A portion of amino acids 529-560 from the human protein was used as the immunogen for this GPC3 antibody.
Isotype
  • Rabbit Ig
Product Type
  • Antibodies
  • Primary Antibodies
Purity Purified
Reactivity
  • Human
  • Mouse
Storage Aliquot the GPC3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Target GPC3
UniProt # P51654

GPC3 is a cell surface proteoglycan that bears heparan sulfate. This protein may be involved in the suppression/modulation of growth in the predominantly mesodermal tissues and organs, and may play a role in the modulation of IGF2 interactions with its receptor and thereby modulate its function. Members of the glypican-related integral membrane proteoglycan family contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol (GPI) linkage. These proteins may play a role in the control of cell division, growth regulation, and tumor predisposition. Deletion mutations in GPC3 are the cause of Simpson-Golabi-Behmel syndrome (SGBS), also known as Simpson dysmorphia syndrome (SDYS). SGBS is a condition characterized by pre- and postnatal overgrowth (gigantism) with visceral and skeletal anomalies.

  • Format: 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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Try Celltrypse Free – Request Your Sample Today

Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

Try Celltrypse Free – Request Your Sample Today