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mouse igm anti–hnk1  (Developmental Studies Hybridoma Bank)


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    Structured Review

    Developmental Studies Hybridoma Bank mouse igm anti–hnk1
    Mouse Igm Anti–Hnk1, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+hnk1/hnk1+antibody/pmc12264845-96-4-7
    Average 90 stars, based on 1 article reviews
    mouse igm anti–hnk1 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Chromatin Immunoprecipitation:

    Article Title: Neural crest origin of sympathetic neurons at the dawn of vertebrates.
    Article Snippet: The neural crest is an embryonic stem cell population unique to vertebrates whose expansion and diversification are thought to have promoted vertebrate evolution by enabling emergence of new cell types and structures such as jaws and peripheral ganglia.. Although jawless vertebrates have sensory ganglia, convention has it that trunk sympathetic chain ganglia arose only in jawed vertebrates.. Here, by contrast, we report the presence of trunk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate.

    Flow Cytometry:

    Article Title: Neural crest origin of sympathetic neurons at the dawn of vertebrates.
    Article Snippet: The neural crest is an embryonic stem cell population unique to vertebrates whose expansion and diversification are thought to have promoted vertebrate evolution by enabling emergence of new cell types and structures such as jaws and peripheral ganglia.. Although jawless vertebrates have sensory ganglia, convention has it that trunk sympathetic chain ganglia arose only in jawed vertebrates.. Here, by contrast, we report the presence of trunk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate.

    Magnetic Resonance Imaging:

    Article Title: Neural crest origin of sympathetic neurons at the dawn of vertebrates.
    Article Snippet: The neural crest is an embryonic stem cell population unique to vertebrates whose expansion and diversification are thought to have promoted vertebrate evolution by enabling emergence of new cell types and structures such as jaws and peripheral ganglia.. Although jawless vertebrates have sensory ganglia, convention has it that trunk sympathetic chain ganglia arose only in jawed vertebrates.. Here, by contrast, we report the presence of trunk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate.

    Biomarker Discovery:

    Article Title: Neural crest origin of sympathetic neurons at the dawn of vertebrates.
    Article Snippet: The neural crest is an embryonic stem cell population unique to vertebrates whose expansion and diversification are thought to have promoted vertebrate evolution by enabling emergence of new cell types and structures such as jaws and peripheral ganglia.. Although jawless vertebrates have sensory ganglia, convention has it that trunk sympathetic chain ganglia arose only in jawed vertebrates.. Here, by contrast, we report the presence of trunk sympathetic neurons in the sea lamprey, Petromyzon marinus, an extant jawless vertebrate.



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    (A) Schematic diagrams of a cross-section through the cranial NT illustrating the migration (B, B’) of NC and their coalescence (C, C’) and condensation (D, D’) with placode cells during TG formation in chicken embryos. Scale bars: 100 μm. Transverse section of miR-203 after in situ hybridization using an LNA-DIG-labeled probe followed by immunostaining for <t>HNK1</t> (neural crest marker in red) and Tuj1 (placodal marker in green) at HH13 (B) , HH16 (C) , and HH20 (D) . Scale bars: 50 μm. While miR-203 is absent from migrating NC cells, its expression reinitiates at the time of ganglion coalescence and remains present in the condensed ganglion. Red and green arrowheads in C’ denoted early coalescing NC and placode cells expressing miR-203, respectively. NC, neural crest; NT, neural tube; TG, trigeminal ganglion.
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    (A) Schematic diagrams of a cross-section through the cranial NT illustrating the migration (B, B’) of NC and their coalescence (C, C’) and condensation (D, D’) with placode cells during TG formation in chicken embryos. Scale bars: 100 μm. Transverse section of miR-203 after in situ hybridization using an LNA-DIG-labeled probe followed by immunostaining for <t>HNK1</t> (neural crest marker in red) and Tuj1 (placodal marker in green) at HH13 (B) , HH16 (C) , and HH20 (D) . Scale bars: 50 μm. While miR-203 is absent from migrating NC cells, its expression reinitiates at the time of ganglion coalescence and remains present in the condensed ganglion. Red and green arrowheads in C’ denoted early coalescing NC and placode cells expressing miR-203, respectively. NC, neural crest; NT, neural tube; TG, trigeminal ganglion.
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    (A) Schematic diagrams of a cross-section through the cranial NT illustrating the migration (B, B’) of NC and their coalescence (C, C’) and condensation (D, D’) with placode cells during TG formation in chicken embryos. Scale bars: 100 μm. Transverse section of miR-203 after in situ hybridization using an LNA-DIG-labeled probe followed by immunostaining for <t>HNK1</t> (neural crest marker in red) and Tuj1 (placodal marker in green) at HH13 (B) , HH16 (C) , and HH20 (D) . Scale bars: 50 μm. While miR-203 is absent from migrating NC cells, its expression reinitiates at the time of ganglion coalescence and remains present in the condensed ganglion. Red and green arrowheads in C’ denoted early coalescing NC and placode cells expressing miR-203, respectively. NC, neural crest; NT, neural tube; TG, trigeminal ganglion.
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    Image Search Results


    (A) Schematic diagrams of a cross-section through the cranial NT illustrating the migration (B, B’) of NC and their coalescence (C, C’) and condensation (D, D’) with placode cells during TG formation in chicken embryos. Scale bars: 100 μm. Transverse section of miR-203 after in situ hybridization using an LNA-DIG-labeled probe followed by immunostaining for HNK1 (neural crest marker in red) and Tuj1 (placodal marker in green) at HH13 (B) , HH16 (C) , and HH20 (D) . Scale bars: 50 μm. While miR-203 is absent from migrating NC cells, its expression reinitiates at the time of ganglion coalescence and remains present in the condensed ganglion. Red and green arrowheads in C’ denoted early coalescing NC and placode cells expressing miR-203, respectively. NC, neural crest; NT, neural tube; TG, trigeminal ganglion.

    Journal: PLOS Biology

    Article Title: miR-203 secreted in extracellular vesicles mediates the communication between neural crest and placode cells required for trigeminal ganglia formation

    doi: 10.1371/journal.pbio.3002074

    Figure Lengend Snippet: (A) Schematic diagrams of a cross-section through the cranial NT illustrating the migration (B, B’) of NC and their coalescence (C, C’) and condensation (D, D’) with placode cells during TG formation in chicken embryos. Scale bars: 100 μm. Transverse section of miR-203 after in situ hybridization using an LNA-DIG-labeled probe followed by immunostaining for HNK1 (neural crest marker in red) and Tuj1 (placodal marker in green) at HH13 (B) , HH16 (C) , and HH20 (D) . Scale bars: 50 μm. While miR-203 is absent from migrating NC cells, its expression reinitiates at the time of ganglion coalescence and remains present in the condensed ganglion. Red and green arrowheads in C’ denoted early coalescing NC and placode cells expressing miR-203, respectively. NC, neural crest; NT, neural tube; TG, trigeminal ganglion.

    Article Snippet: Embryos were then incubated in mouse anti-Tuj1 (1:250; Covance) and/or mouse anti-HNK1 (1:10; supplied by the Developmental Studies Hybridoma Bank) overnight at 4°C diluted in TBST-FBS.

    Techniques: Migration, In Situ Hybridization, Labeling, Immunostaining, Marker, Expressing

    Journal: STAR Protocols

    Article Title: Generation of human iPSC-derived neurofibromaspheres for in vitro and in vivo uses

    doi: 10.1016/j.xpro.2023.102198

    Figure Lengend Snippet:

    Article Snippet: Mouse IgG anti-HNK1 , Sigma , Cat# C6680 RRID: AB_1078474.

    Techniques: Recombinant, Plasmid Preparation, Purification, Expressing, Software