Anti-Mouse Jagged 2 – Purified in vivo GOLD™ Functional Grade
Anti-Mouse Jagged 2 – Purified in vivo GOLD™ Functional Grade
Product No.: J131
Clone HMJ2-1 Target Jagged 2 Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names N/A Isotype Armenian Hamster IgG Applications B , FC |
Antibody DetailsProduct DetailsReactive Species Mouse Host Species Armenian Hamster Recommended Dilution Buffer Immunogen CHO derived Mouse Jag2 Product Concentration ≥ 5.0 mg/ml Endotoxin Level < 1.0 EU/mg as determined by the LAL method Purity ≥95% monomer by analytical SEC ⋅ >95% by SDS Page Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration. State of Matter Liquid Product Preparation Functional grade preclinical antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2 – 8° C Wet Ice Additional Applications Reported In Literature ? B, FC Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity HMJ2-1 activity is directed against mouse Jagged2. Background The Notch pathway is an intercellular signaling mechanism that controls cell fate and
differentiation during embryonic and postnatal development1,2,3. The pathway is highly
conserved across species. Four mammalian Notch receptors (Notch 1-4) have been identified and
can be activated by their ligands Jagged1, Jagged2, DLL1, DLL3, or DLL4. These ligands are
transmembrane proteins that contain a Delta/Serrate/Lag-2 extracellular domain that is used for
interactions with the Notch receptors3. Receptor-ligand engagement triggers cleavage of the
Notch receptor extracellular domain, leading to the release of the Notch intracellular domain
which travels to the nucleus and affects target gene expression. Dysregulation of Notch signaling
affects inflammation3 as well as tumorigenesis and cancer growth1,4. HMJ2-1 was generated using CHO cells expressing murine Jagged25. Antigen Distribution Jagged2 is expressed by stromal and thymic lymphoid cells, splenic
macrophages, and dendritic cells. Jagged2 can also be expressed by cancer stem cells and is
upregulated on antigen-presenting cells after transplantation. Ligand/Receptor Notch receptors NCBI Gene Bank ID UniProt.org Research Area Cancer . Immunology . Development Leinco Antibody AdvisorPowered by AI: AI is experimental and still learning how to provide the best assistance. It may occasionally generate incorrect or incomplete responses. Please do not rely solely on its recommendations when making purchasing decisions or designing experiments. Clone HMJ2-1 is a monoclonal antibody that specifically recognizes mouse Jagged2 (JAG2), a ligand for the Notch signaling pathway. The most common in vivo applications of clone HMJ2-1 in mice are still limited and primarily focused on research use, with well-established applications in flow cytometry and mechanistic studies of the Notch pathway—but little direct evidence from the search results of routine use for direct in vivo administration in mice. Primary Reported Applications
Potential and Investigational In Vivo Applications
Limitations and Research-Only Use
Indirect or Related Uses
Summary Table
In summary: The most common applications of clone HMJ2-1 in mouse studies are detection and quantification of Jagged2 expression by flow cytometry and protein analysis, with no current standard validated use for direct in vivo administration or functional modulation in mice according to available sources. Based on the available search results, specific information about antibodies or proteins commonly used in combination with HMJ2-1 in published literature is limited. The search results primarily focus on the characteristics and applications of HMJ2-1 itself rather than its use alongside other antibodies in experimental contexts. What We Know About HMJ2-1HMJ2-1 is an Armenian hamster monoclonal antibody that specifically targets mouse Jagged-2, a type I transmembrane protein that serves as a Notch receptor ligand. The antibody has been validated for several applications including flow cytometry, ELISA, and as an agonist that promotes Treg cell differentiation and enhances Jagged-2 Notch signaling via activation of RBP-Jk. Limited Information on Co-usageThe search results do not provide detailed information about other antibodies or proteins routinely paired with HMJ2-1 in multi-marker studies or combination experiments. While the results mention that HMJ2-1 has been used in various research contexts involving the Notch signaling pathway, they do not specify which other antibodies investigators typically employ alongside it for co-staining, co-immunoprecipitation, or other combinatorial approaches. To identify commonly co-used antibodies or proteins with HMJ2-1, you would need to review primary research articles that cite the use of this antibody in Notch signaling studies, T cell research, or developmental biology investigations where multiple markers are typically analyzed simultaneously. Clone HMJ2-1 is a monoclonal antibody widely cited in scientific literature for its specificity in detecting Jagged2, a ligand in the Notch signaling pathway. The antibody is principally used in mouse models for applications such as flow cytometry, ELISA, and inhibition assays. Key findings and details from scientific literature referencing clone HMJ2-1:
The literature underscores HMJ2-1's importance for research involving Notch pathway biology, specifically for dissecting Jagged2's role in cell signaling and immune modulation. No major conflicting findings were reported, but direct source citations of HMJ2-1 in primary research typically focus on its use as a detection and characterization tool rather than as a direct modulator of function. Based on the available search results, there is no specific information about dosing regimens for clone HMJ2-1 across different mouse models. Clone HMJ2-1 is identified as an Armenian Hamster monoclonal antibody that specifically detects mouse Jagged2, but the search results do not provide details about its dosing protocols, administration routes, or treatment schedules in experimental settings. While the search results contain extensive information about dosing regimens for other antibodies used in mouse models—particularly checkpoint blockade antibodies like anti-PD-1 (200-500 μg per mouse) and anti-CTLA-4 (100-250 μg per mouse)—no comparable data is available for HMJ2-1. The search results explicitly note that dosing regimens for clone HMJ2-1 in different mouse models are not documented in the provided sources. To obtain accurate dosing information for HMJ2-1, researchers would need to consult the original research publications that have used this antibody in vivo, contact the antibody manufacturer directly, or establish dosing parameters through pilot studies based on the antibody's binding characteristics and the specific experimental objectives. References & Citations1. Fazio C, Ricciardiello L. Cell Death Dis. 7(12):e2515. 2016. 2. https://www.ncbi.nlm.nih.gov/gene/3714 3. Sekine C, Nanki T, Yagita H. Arthritis Rheumatol. 66(10):2751-2761. 2014. 4. Mandula JK, Sierra-Mondragon RA, Jimenez RV, et al. Immunity. 57(5):1124-1140.e9. 2024. 5. Moriyama Y, Sekine C, Koyanagi A, et al. Int Immunol. 20(6):763-773. 2008. 6. Sekine C, Moriyama Y, Koyanagi A, et al. Int Immunol. 21(3):295-301. 2009. 7. Sekine C, Koyanagi A, Koyama N, et al. Arthritis Res Ther. 14(2):R45. 2012. 8. Kijima M, Yamaguchi T, Ishifune C, et al. Proc Natl Acad Sci U S A. 105(19):7010-7015. 2008. 9. Riella LV, Yang J, Chock S, et al. Eur J Immunol. 43(6):1449-1458. 2013. 10. Steinbuck MP, Arakcheeva K, Winandy S. J Immunol. 200(3):997-1007. 2018. Technical ProtocolsCertificate of Analysis |
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