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mouse anti jag1  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc mouse anti jag1
    Mouse Anti Jag1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 134 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+jag1/10__2174_slash_1574888x18666221216123259-76-11-14?v=Cell+Signaling+Technology+Inc
    Average 95 stars, based on 134 article reviews
    mouse anti jag1 - by Bioz Stars, 2026-08
    95/100 stars

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    Network functions of candidate mesoderm‐specific genes by GO and IPA and their confirmation by qRT‐PCR and IHC. (A) GO cluster analysis of candidate mesoderm‐specific genes. (B) Top 1 network generated by IPA for the 50 mesoderm DEGs. The IPA network is graphically represented as nodes (proteins) and edges (the biological relationship between the nodes) and generated based on their functional and biological connectivity. The length of an edge reflects the evidence in the literature supporting that node‐to‐node relationship. Shaded notes represented mesoderm‐related genes screened by three analytical pipelines, while others (empty nodes) were not assessed in this study but identified by IPA as important nodes involved in the network. (C) qPCR expression analysis for selected mesoderm candidate genes ( Cdh2 , Cdh11 , <t>Jag1</t> , and Pcdh7 ) in three germ layers. The mRNA expression of mesoderm candidate genes relative to β‐actin expression level. (D) IHC protein expression for selected candidate genes ( T , Fn1 , and Cdh2 ) in cross‐section of E7.5 embryo. Data are shown as mean ± SD. * p < 0.05, ** p < 0.01
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    Cell Signaling Technology Inc rabbit monoclonal anti human mouse jag1
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    Image Search Results


    Journal: Cell reports

    Article Title: TGF-β1-mediated intercellular signaling fuels cooperative cellular invasion

    doi: 10.1016/j.celrep.2025.115315

    Figure Lengend Snippet:

    Article Snippet: Anti-Jagged 1/JAG1 Antibody (PE) , Sino Biological , Cat11648-MM03-P; RRID: AB_2860365.

    Techniques: Recombinant, Reverse Transcription, Bicinchoninic Acid Protein Assay, Staining, RNA Sequencing

    Journal: Cell reports

    Article Title: TGF-β1-mediated intercellular signaling fuels cooperative cellular invasion

    doi: 10.1016/j.celrep.2025.115315

    Figure Lengend Snippet:

    Article Snippet: Anti-Jagged 1/JAG1 Antibody (PE) , Sino Biological , Cat#11648-MM03-P; RRID: AB_2860365.

    Techniques: Recombinant, Reverse Transcription, Bicinchoninic Acid Protein Assay, Staining, RNA Sequencing

    Journal: eLife

    Article Title: The Jag2/Notch1 signaling axis promotes sebaceous gland differentiation and controls progenitor proliferation

    doi: 10.7554/eLife.98747

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-Jag1 (Mouse monoclonal) , Genentech , , Inhibiting antibody (20 mg/kg).

    Techniques: Control, Staining, Sequencing, RNAscope, Multiplex Assay

    Journal: Cell reports

    Article Title: Notch receptor-ligand binding facilitates extracellular vesicle-mediated neuron-to-neuron communication

    doi: 10.1016/j.celrep.2024.113680

    Figure Lengend Snippet:

    Article Snippet: Mouse anti-Jag1 , Santa Cruz Biotechnology , Cat# sc-390177; RRID: AB_2892141.

    Techniques: Virus, Recombinant, Protease Inhibitor, Lactate Dehydrogenase Assay, Magnetic Beads, Silver Staining, Phospho-proteomics, Peptide Fractionation, RNA Sequencing, Mass Spectrometry, Software, Sequencing, Transmission Assay, Imaging, Microscopy

    Network functions of candidate mesoderm‐specific genes by GO and IPA and their confirmation by qRT‐PCR and IHC. (A) GO cluster analysis of candidate mesoderm‐specific genes. (B) Top 1 network generated by IPA for the 50 mesoderm DEGs. The IPA network is graphically represented as nodes (proteins) and edges (the biological relationship between the nodes) and generated based on their functional and biological connectivity. The length of an edge reflects the evidence in the literature supporting that node‐to‐node relationship. Shaded notes represented mesoderm‐related genes screened by three analytical pipelines, while others (empty nodes) were not assessed in this study but identified by IPA as important nodes involved in the network. (C) qPCR expression analysis for selected mesoderm candidate genes ( Cdh2 , Cdh11 , Jag1 , and Pcdh7 ) in three germ layers. The mRNA expression of mesoderm candidate genes relative to β‐actin expression level. (D) IHC protein expression for selected candidate genes ( T , Fn1 , and Cdh2 ) in cross‐section of E7.5 embryo. Data are shown as mean ± SD. * p < 0.05, ** p < 0.01

    Journal: Cell Proliferation

    Article Title: Spatial transcriptomic profiling to identify mesoderm progenitors with precision genomic screening and functional confirmation

    doi: 10.1111/cpr.13298

    Figure Lengend Snippet: Network functions of candidate mesoderm‐specific genes by GO and IPA and their confirmation by qRT‐PCR and IHC. (A) GO cluster analysis of candidate mesoderm‐specific genes. (B) Top 1 network generated by IPA for the 50 mesoderm DEGs. The IPA network is graphically represented as nodes (proteins) and edges (the biological relationship between the nodes) and generated based on their functional and biological connectivity. The length of an edge reflects the evidence in the literature supporting that node‐to‐node relationship. Shaded notes represented mesoderm‐related genes screened by three analytical pipelines, while others (empty nodes) were not assessed in this study but identified by IPA as important nodes involved in the network. (C) qPCR expression analysis for selected mesoderm candidate genes ( Cdh2 , Cdh11 , Jag1 , and Pcdh7 ) in three germ layers. The mRNA expression of mesoderm candidate genes relative to β‐actin expression level. (D) IHC protein expression for selected candidate genes ( T , Fn1 , and Cdh2 ) in cross‐section of E7.5 embryo. Data are shown as mean ± SD. * p < 0.05, ** p < 0.01

    Article Snippet: Antibodies used were the following: anti‐mouse FLK‐1 (BD Pharmingen), anti‐mouse CDH2 (abcam), anti‐mouse CDH11 (Invitrogen), anti‐mouse JAG1 (eBioscience), anti‐mouse PCDH7 (biorbyt).

    Techniques: Quantitative RT-PCR, Generated, Functional Assay, Expressing

    Identification of candidate mesoderm‐specific genes ESCs‐EBs differentiation. (A) Flow cytometry analysis of FLK‐1, CDH2, CDH11, JAG1, and PCDH7 combined with T during embryonic body differentiation from Day (D) 2 to Day 5. (B) Percentage of FLK‐1 + , CDH2 + , CDH11 + , JAG1 + , and PCDH7 + cells in embryonic bodies from Day 2 to Day 5. (c) Percentage of T + cells in FLK‐1 + , CDH2 + , CDH11 + , JAG1 + , and PCDH7 + cells from Day 2 to Day 5

    Journal: Cell Proliferation

    Article Title: Spatial transcriptomic profiling to identify mesoderm progenitors with precision genomic screening and functional confirmation

    doi: 10.1111/cpr.13298

    Figure Lengend Snippet: Identification of candidate mesoderm‐specific genes ESCs‐EBs differentiation. (A) Flow cytometry analysis of FLK‐1, CDH2, CDH11, JAG1, and PCDH7 combined with T during embryonic body differentiation from Day (D) 2 to Day 5. (B) Percentage of FLK‐1 + , CDH2 + , CDH11 + , JAG1 + , and PCDH7 + cells in embryonic bodies from Day 2 to Day 5. (c) Percentage of T + cells in FLK‐1 + , CDH2 + , CDH11 + , JAG1 + , and PCDH7 + cells from Day 2 to Day 5

    Article Snippet: Antibodies used were the following: anti‐mouse FLK‐1 (BD Pharmingen), anti‐mouse CDH2 (abcam), anti‐mouse CDH11 (Invitrogen), anti‐mouse JAG1 (eBioscience), anti‐mouse PCDH7 (biorbyt).

    Techniques: Flow Cytometry

    KEY RESOURCES TABLE

    Journal: Molecular cell

    Article Title: Systematic Characterization of Mutations Altering Protein Degradation in Human Cancers

    doi: 10.1016/j.molcel.2021.01.020

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit monoclonal anti-human/mouse JAG1 , Cell Signaling Technology , Cat#70109.

    Techniques: Control, Virus, Recombinant, In Vitro, Transfection, Western Blot, Capsules, Purification, Gel Extraction, cDNA Synthesis, RNA HS Assay, Plasmid Preparation, BIA-KA, Software, Adhesive