NPC1 Antibody / Niemann Pick C1

SKU:BHA17100565
Suppliers
NSJ Bioreagents
NSJ Bioreagents
Details Products
Overview
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Anti-NPC1 polyclonal antibody (Rabbit Ig) for target detection, validation, and assay development. Reactivity: Human; antigen-affinity purified reagent to support IF, IHC, WB, and ELISA.
Target NPC1
Host Rabbit
Isotype Rabbit Ig
Reactivity Human
Application(s) IF, IHC, WB, ELISA
Options selector
Catalog no. Formulation Size
F42992-0.08ML 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 F42992
Clonality
  • Polyclonal (rabbit origin)
Host Rabbit
Immunogen A portion of amino acids 591-620 from the human protein was used as the immunogen for this NPC1 antibody.
Isotype
  • Rabbit Ig
Product Type
  • Antibodies
  • Primary Antibodies
Purity Antigen affinity
Reactivity
  • Human
Storage Aliquot the NPC1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Target NPC1
UniProt # O15118

This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.

  • 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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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.

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