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recombinant human sonic hh protein shh n  (R&D Systems)


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    R&D Systems recombinant human sonic hh protein shh n
    Recombinant Human Sonic Hh Protein Shh N, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/recombinant human sonic hh protein shh n/product/R&D Systems
    Average 94 stars, based on 44 article reviews
    recombinant human sonic hh protein shh n - by Bioz Stars, 2026-03
    94/100 stars

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    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
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    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
    Recombinant Mouse Shh, supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
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    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
    Recombinant Human Sonic Hh Protein Shh N, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    R&D Systems shh c25ii
    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
    Shh C25ii, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PeproTech recombinant shh
    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human <t>recombinant</t> Sonic Hedgehog <t>(SHH,</t> 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.
    Recombinant Shh, supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PeproTech recombinant murine sonic hedgehog (shh)

    Recombinant Murine Sonic Hedgehog (Shh), supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human recombinant Sonic Hedgehog (SHH, 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.

    Journal: bioRxiv

    Article Title: Mapping the temporal and functional landscape of Sonic Hedgehog signaling reveals new insights into early human forebrain development

    doi: 10.1101/2025.05.20.654466

    Figure Lengend Snippet: (A) Schematic illustration of the differentiation protocol for generating dorsal (dAN) and ventral (vAN) anterior neuroectoderm from hiPSCs over a 12-day period. Neural induction and ventralization are initiated by a combination of small molecules: LDN193189 (500 nM), SB431542 (10 µM), from day 0 to day 12, and XAV939 (5 µM) from day 0 to day 5. Additional exposure to human recombinant Sonic Hedgehog (SHH, 500 ng/ml) from day 0 to day 6 selectively drives ventral patterning in vAN cultures. (B) Representative Immunofluorescent images at day 12 show distinct marker expression in dAN and vAN cells. Markers analyzed include OTX2 (anterior neuroectoderm marker), PAX6 and EMX2 (dorsal forebrain markers), EOMES (early neural cortical marker), MEIS2 (forebrain marker), NKX2.1 (ventral forebrain marker), FOXA2 (floor plate marker), and SHH (ventral marker). Expression levels are quantified as the percentage of positively stained cells relative to DAPI (mean values from 5 independent images). Scale bar: 40 µm. (C) Principal Component Analysis (PCA) of day 12 dAN and vAN samples (LON and WTC lines) from 5 replicates revealed clear segregation by identity and lineage. PC1 (52% total variance) strongly distinguished dAN versus vAN conditions (one-way ANOVA p.value of 8.9e-12), while PC2 (30% total variance) separates samples by cell lineage origin (one-way ANOVA p.value of 3.1e-12). (D) Heatmap displaying normalized RNA-seq expression profiles of day 12 dAN and vAN samples. Samples were manually ordered by type (vAN/dAN) and cell line (LON/WTC). Marker genes sets specific for hiPSCs, forebrain, ventral/dorsal Forebrain, Midbrain and Hindbrain identity were curated from literature. (E) Heatmap of scaled normalized RNA-seq data showing differentially expressed genes (DEGs) between day 12 dAN and vAN samples (|log2FC| ≥ 1, FDR < 0.01), across 2 hiPSC lines (LON, WTC). Both genes and samples were hierarchical clustered (cluster vAN and cluster dAN), two cluster were identified and then delimited using cutree R function with k=2. (F) Brain development-related Gene Ontology terms among the top 20 most enriched (in term of gene ratio) biological process for both DEGs clusters (dAN and vAN). Color scale indicates gene sets enrichment statistical significance.

    Article Snippet: To induce ventralisation and generate ventral anterior neuroectoderm 500ng/ml of human recombinant SHH (C24II, #78065, STEMCELL) was added to media mix from day 0 to day 6.

    Techniques: Recombinant, Marker, Expressing, Staining, RNA Sequencing

    Journal: STAR Protocols

    Article Title: Protocol for generating human craniofacial cartilage organoids from stem-cell-derived neural crest cells

    doi: 10.1016/j.xpro.2024.103532

    Figure Lengend Snippet:

    Article Snippet: Recombinant Murine Sonic Hedgehog (Shh) , Peprotech , Cat# 315–22, UniProt ID: Q62226.

    Techniques: Recombinant, Knock-Out, Membrane, Selection

    Neural crest stem cell (NCSC) specification medium

    Journal: STAR Protocols

    Article Title: Protocol for generating human craniofacial cartilage organoids from stem-cell-derived neural crest cells

    doi: 10.1016/j.xpro.2024.103532

    Figure Lengend Snippet: Neural crest stem cell (NCSC) specification medium

    Article Snippet: Recombinant Murine Sonic Hedgehog (Shh) , Peprotech , Cat# 315–22, UniProt ID: Q62226.

    Techniques: Concentration Assay, Recombinant

    Neural crest stem cell (NCSC) maintenance medium

    Journal: STAR Protocols

    Article Title: Protocol for generating human craniofacial cartilage organoids from stem-cell-derived neural crest cells

    doi: 10.1016/j.xpro.2024.103532

    Figure Lengend Snippet: Neural crest stem cell (NCSC) maintenance medium

    Article Snippet: Recombinant Murine Sonic Hedgehog (Shh) , Peprotech , Cat# 315–22, UniProt ID: Q62226.

    Techniques: Concentration Assay, Recombinant