Human/Mouse Meprin beta Subunit/MEP1B Antibody Summary
Thr23-Ser293
Accession # Q16820
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
Detection of Human and Mouse Meprin beta Subunit/ MEP1B by Western Blot. Western blot shows lysates of human intestine tissue and mouse intestine tissue. PVDF membrane was probed with 1 µg/mL of Rat Anti-Human/Mouse Meprin beta Subunit/MEP1B Monoclonal Antibody (Catalog # MAB28951) followed by HRP-conjugated Anti-Rat IgG Secondary Antibody (Catalog # HAF005). A specific band was detected for Meprin beta Subunit/MEP1B at approximately 97 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Meprin beta Subunit/MEP1B in Human Intestine. Meprin beta Subunit/MEP1B was detected in immersion fixed paraffin-embedded sections of human intestine using Human/Mouse Meprin beta Subunit/MEP1B Monoclonal Antibody (Catalog # MAB28951) at 1 µg/mL overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (Catalog # CTS013). Tissue was stained using the Anti-Rat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS017) and counterstained with hemotoxylin (blue). Specific staining was localized to the Brush border of epithelial cells. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections. This application has not been tested in mouse samples
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: Meprin beta Subunit/MEP1B
Meprins are multimeric proteases composed of alpha and beta subunits, which are members of the astacin family of zinc endopeptidases (1, 2). Both subunits form disulfide-linked homo- or heterooligomers, which are also referred to as Meprin A (composed of alpha subunits with or without beta subunits) and Merpin B (composed of beta subunits only) (3). Although the two subunits share 42% amino acid (aa) sequence identity, they differ significantly in their oligomeric structure, post-translational processing and subsequently cellular location, and substrate and peptide bond specificity (4). The 701 aa sequence of human Merpin beta subunit precursor consists of a signal peptide (aa 1 to 21), a pro region (aa 22 to 61), and a mature chain (aa 62 to 701) containing catalytic (aa 62 to 259), MAM (aa 260 to 429), MATH (aa 430 to 585), EGF-like (aa 604 to 644), transmembrane (aa 653 to 673), and cytoplasmic (aa 674 to 701) domains.
- Bond, J.S. and R.J. Beynon (1995) Protein Sci. 4:1247.
- Stocker, W. et al. (1995) Protein Sci. 4:823.
- Bertenshaw, G.P. et al. (2001) J. Biol. Chem. 276:13248.
- Ishmael, F.T. et al. (2005) J. Biol. Chem. 280:13895.
Product Datasheets
Citations for Human/Mouse Meprin beta Subunit/MEP1B 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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Uterine luminal-derived extracellular vesicles: potential nanomaterials to improve embryo implantation
Authors: Linjun Hong, Xupeng Zang, Qun Hu, Yanjuan He, Zhiqian Xu, Yanshe Xie et al.
Journal of Nanobiotechnology
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Distinct contributions of meprins to skin regeneration after injury – Meprin alpha a physiological processer of pro-collagen VII
Authors: Daniel Kruppa, Florian Peters, Olivier Bornert, Mareike D. Maler, Stefan F. Martin, Christoph Becker-Pauly et al.
Matrix Biology Plus
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High-fat diet modifies the PPAR-gamma pathway leading to disruption of microbial and physiological ecosystem in murine small intestine
Authors: Tomas J, Mulet C, Saffarian A et al.
Proc. Natl. Acad. Sci. U.S.A.
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Genetic Background is a Key Determinant of Glomerular Extracellular Matrix Composition and Organization
Authors: Michael J. Randles, Adrian S. Woolf, Jennifer L. Huang, Adam Byron, Jonathan D. Humphries, Karen L. Price et al.
Journal of the American Society of Nephrology
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