Human Trypsin 1/PRSS1 Antibody Summary
Ala16-Ser247
Accession # P07477
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Trypsin 1/PRSS1 in Human Pancreas. Trypsin 1/PRSS1 was detected in immersion fixed paraffin-embedded sections of human pancreas using Mouse Anti-Human Trypsin 1/PRSS1 Monoclonal Antibody (Catalog # MAB3848) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Sheep HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS019) and counterstained with hematoxylin (blue). Specific staining was localized to exocrine cells. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: Trypsin 1/PRSS1
Human Trypsin 1, encoded by the PRSS1 gene, is also known as Cationic Trypsinogen (1). Constituting approximately two-thirds of the total trypsin content in normal pancreatic juice, it is the most abundant trypsin isoform produced by the pancreas. It contains a signal peptide (residues 1‑15), a pro region (residues 16‑23), and a mature chain (residues 24‑247). Trypsin 1 is synthesized in the pancreas and secreted into the duodenum lumen, where it is activated by enterokinase. Its major physiologic function is to digest food and to activate other pro-enzymes (2). Mutations in the PRSS1 gene can cause hereditary pancreatitis (3).
- Emi, M. et al. (1986) Gene 41:305.
- Halfon, S. et al. (2004) in Handbook of Proteolytic Enzymes (ed. Barrett, et al.) p. 1483, Academic Press, San Diego.
- Teich, N. et al. (2006) Hum. Mutat. 27:721.
Product Datasheets
Citations for Human Trypsin 1/PRSS1 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 7
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Robust autoactivation, chymotrypsin C independence and diminished secretion define a subset of hereditary pancreatitis-associated cationic trypsinogen mutants
Authors: Andrea Geisz, Péter Hegyi, Miklós Sahin-Tóth
FEBS Journal
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SARS-CoV-2 infection induces beta cell transdifferentiation
Authors: Tang X, Uhl S, Zhang T et al.
Cell Metabolism
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Intragenic duplication: a novel mutational mechanism in hereditary pancreatitis
Authors: Maiken T. Joergensen, Andrea Geisz, Klaus Brusgaard, Ove B. Schaffalitzky Schaffalitzky de Muckadell, Péter Hegyi, Anne-Marie Gerdes et al.
Pancreas
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Expression of human cationic trypsinogen (PRSS1) in murine acinar cells promotes pancreatitis and apoptotic cell death
Authors: T Athwal, W Huang, R Mukherjee, D Latawiec, M Chvanov, R Clarke et al.
Cell Death & Disease
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Pathogenic cellular role of the p.L104P human cationic trypsinogen variant in chronic pancreatitis
Authors: Anita Balázs, Péter Hegyi, Miklós Sahin-Tóth
American Journal of Physiology-Gastrointestinal and Liver Physiology
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Developmental History Provides a Roadmap for the Emergence of Tumor Plasticity
Authors: PR Tata, RD Chow, SV Saladi, A Tata, A Konkimalla, A Bara, D Montoro, LP Hariri, AR Shih, M Mino-Kenud, H Mou, S Kimura, LW Ellisen, J Rajagopal
Dev. Cell, 2018-03-26;44(6):679-693.e5.
Species: Human
Sample Types: Whole Tissue
Applications: IHC-Fr -
Functional effects of 13 rare PRSS1 variants presumed to cause chronic pancreatitis
Authors: Andrea Schnúr, Sebastian Beer, Heiko Witt, Péter Hegyi, Miklós Sahin-Tóth
Gut
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