Date published: 2026-3-17

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PRPF3 Antibody (42-N): sc-101130

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Datasheets
  • PRPF3 Antibody (42-N) is a mouse monoclonal IgG3 κ PRPF3 antibody, cited in 1 publications, provided at 100 µg/ml
  • raised against recombinant PRPF3 of human origin
  • recommended for detection of PRPF3 of mouse, rat and human origin by WB, IP and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for PRPF3 Antibody (42-N). This work is in progress.
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PRPF3 Antibody (42-N) is a mouse monoclonal IgG3 kappa light chain antibody that detects PRPF3 protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), and enzyme-linked immunosorbent assay (ELISA). PRPF3 (42-N) antibody is available as the non-conjugated anti-PRPF3 monoclonal isotype antibody. PRPF3 protein, also known as PRP3 pre-mRNA processing factor 3 homolog, RP18, PRP3, Prp3p, HPRP3, or HPRP3P, plays a crucial role in pre-mRNA splicing as a component of the U4/U6.U5 tri-snRNP complex, which is essential for accurate processing of pre-mRNA into mature mRNA. PRPF3 is ubiquitously expressed, with significant levels found in retina, blood, kidney, and liver, and localizes primarily to nuclear speckles. Notably, PRPF3 undergoes phosphorylation, a post-translational modification that can influence function and interactions within the spliceosome. PRPF3 directly interacts with PRPF4 and is present in the inactive spliceosome, highlighting importance in the splicing process, particularly in photoreceptor-specific genes. Mutations in the gene encoding PRPF3 are linked to autosomal dominant retinitis pigmentosa type 18 (RP18), a condition characterized by progressive photoreceptor cell degeneration, initially manifesting as a loss of midperipheral vision and night blindness, ultimately leading to severe vision impairment. This underscores the critical role of PRPF3 in maintaining retinal health and potential as a target for therapeutic intervention in retinal diseases.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

PRPF3 Antibody (42-N) References:

  1. Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.  |  Chakarova, CF., et al. 2002. Hum Mol Genet. 11: 87-92. PMID: 11773002
  2. Central region of the human splicing factor Hprp3p interacts with Hprp4p.  |  Gonzalez-Santos, JM., et al. 2002. J Biol Chem. 277: 23764-72. PMID: 11971898
  3. Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells.  |  Comitato, A., et al. 2007. Hum Mol Genet. 16: 1699-707. PMID: 17517693
  4. Mutation in the splicing factor Hprp3p linked to retinitis pigmentosa impairs interactions within the U4/U6 snRNP complex.  |  Gonzalez-Santos, JM., et al. 2008. Hum Mol Genet. 17: 225-39. PMID: 17932117
  5. Hypoxia-regulated components of the U4/U6.U5 tri-small nuclear riboprotein complex: possible role in autosomal dominant retinitis pigmentosa.  |  Schmidt-Kastner, R., et al. 2008. Mol Vis. 14: 125-35. PMID: 18334927
  6. The human U4/U6 snRNP contains 60 and 90kD proteins that are structurally homologous to the yeast splicing factors Prp4p and Prp3p.  |  Lauber, J., et al. 1997. RNA. 3: 926-41. PMID: 9257651
  7. Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome.  |  Wang, A., et al. 1997. Hum Mol Genet. 6: 2117-26. PMID: 9328476
  8. A new cyclophilin and the human homologues of yeast Prp3 and Prp4 form a complex associated with U4/U6 snRNPs.  |  Horowitz, DS., et al. 1997. RNA. 3: 1374-87. PMID: 9404889

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

PRPF3 Antibody (42-N)

sc-101130
100 µg/ml
$339.00