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anti cdx2  (R&D Systems)


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    R&D Systems anti cdx2
    Anti Cdx2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+cdx2/Human+CDX2+Antibody/bio_rxiv__64898__2026__01__20__700679-246-42-44
    Average 94 stars, based on 14 article reviews
    anti cdx2 - by Bioz Stars, 2026-09
    94/100 stars

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    Produced:

    Article Title: Cell Adhesion Minimization by a Novel Mesh Culture Method Mechanically Directs Trophoblast Differentiation and Self-Assembly Organization of Human Pluripotent Stem Cells
    Article Snippet: The samples were then separately incubated overnight at 4°C with primary antibodies against OCT4, Nanog, CDX2, human chorionic gonadotropin (hCG)-β,E-cadherin, and vinculin, followed by incubation for 60 min with the corresponding secondary antibodies tagged with Alexa Flour dyes (Invitrogen) at 1:500 dilution. .. Primary antibodies used in this study were mouse anti human OCT4 (Santa Cruz) at 1:50 dilution, goat anti human CDX2 (R&D Systems) at 1:200 dilution, rabbit anti human NANOG (Cell Signaling Technology) at 1:100 dilution, polyclonal rabbit anti human CG (Abcam) at 1:200 dilution, monoclonal Anti-vinculin antibody produced in mouse (clone hVIN-1; Sigma Aldrich), and mouse monoclonal anti-human E-cadherin (Takara Bio) at a dilution of 1:200 dilution. ..

    Article Title: Cell Adhesion Minimization by a Novel Mesh Culture Method Mechanically Directs Trophoblast Differentiation and Self-Assembly Organization of Human Pluripotent Stem Cells
    Article Snippet: The samples were then separately incubated overnight at 4 C with primary antibodies against OCT4, Nanog, CDX2, human chorionic gonadotropin (hCG)-b,E-cadherin, and vinculin, followed by incubation for 60 min with the corresponding secondary antibodies tagged with Alexa Flour dyes (Invitrogen) at 1:500 dilution. .. Primary antibodies used in this study were mouse anti human OCT4 (Santa Cruz) at 1:50 dilution, goat anti human CDX2 (R&D Systems) at 1:200 dilution, rabbit anti human NANOG (Cell Signaling Technology) at 1:100 dilution, polyclonal rabbit anti human CG (Abcam) at 1:200 dilution, monoclonal Anti-vinculin antibody produced in mouse (clone hVIN-1; Sigma Aldrich), and mouse monoclonal anti-human E-cadherin (Takara Bio) at a dilution of 1:200 dilution. ..



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    a . Left: total cell number in E3.5 embryos (X m Y n=57, X m X p n= 31, X p O=10, X p O Xist Δ n= 14 embryos); mean value indicated by a red diamond; p -value generated using Student’s t-test. Right: Z-projection of confocal sections (1µm thickness) of E3.5 embryos stained for <t>CDX2</t> (outside cells), and NANOG (inside cells); scale bar: 20µm. b . UMAP showing E3.5 X p O (blue) and X p O Xist Δ (magenta) cells relative to all other genotypes at E3.5 (green) and other time points (grey). c . Proportion of cells within each cluster (uncommitted, ICM, TE) per genotype at E3.5, derived from UMAP in b . d . Normalised expression of early ( Cdx2 ) and late ( Eomes , Elf5 ) TE genes in E3.5 TE cluster cells. e . X-to-autosome (X:A) ratios of X p O and X p O Xist Δ embryos; P values derived from Student’s t-test; one point was excluded as it is outside the represented range. f . Left: quantitation of inactive X-associated ubiquitylated histone H2A at lysine-119 (uH2A) staining in E3.5 embryos (X m Y n=12, X m X p n=10, X p O n=4 embryos); mean value indicated by a red diamond. Right: Z-projection of confocal sections (1µm thickness – total thickness of 10 and 4.5µm respectively) of E3.5 embryos showing uH2A staining. Presence and absence of inactive X-associated uH2A shown by magenta and white circles, respectively. Inserts show a representative image of cells without and with a uH2A cloud. g . E10.5 embryo weights in mg (log 10 ) by genotypes; mean value indicated by a red diamond; P values derived from Wilcoxon test.
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    Image Search Results


    a . Left: total cell number in E3.5 embryos (X m Y n=57, X m X p n= 31, X p O=10, X p O Xist Δ n= 14 embryos); mean value indicated by a red diamond; p -value generated using Student’s t-test. Right: Z-projection of confocal sections (1µm thickness) of E3.5 embryos stained for CDX2 (outside cells), and NANOG (inside cells); scale bar: 20µm. b . UMAP showing E3.5 X p O (blue) and X p O Xist Δ (magenta) cells relative to all other genotypes at E3.5 (green) and other time points (grey). c . Proportion of cells within each cluster (uncommitted, ICM, TE) per genotype at E3.5, derived from UMAP in b . d . Normalised expression of early ( Cdx2 ) and late ( Eomes , Elf5 ) TE genes in E3.5 TE cluster cells. e . X-to-autosome (X:A) ratios of X p O and X p O Xist Δ embryos; P values derived from Student’s t-test; one point was excluded as it is outside the represented range. f . Left: quantitation of inactive X-associated ubiquitylated histone H2A at lysine-119 (uH2A) staining in E3.5 embryos (X m Y n=12, X m X p n=10, X p O n=4 embryos); mean value indicated by a red diamond. Right: Z-projection of confocal sections (1µm thickness – total thickness of 10 and 4.5µm respectively) of E3.5 embryos showing uH2A staining. Presence and absence of inactive X-associated uH2A shown by magenta and white circles, respectively. Inserts show a representative image of cells without and with a uH2A cloud. g . E10.5 embryo weights in mg (log 10 ) by genotypes; mean value indicated by a red diamond; P values derived from Wilcoxon test.

    Journal: bioRxiv

    Article Title: Sex chromosomes shape the transcriptional landscape of the preimplantation mouse embryo

    doi: 10.1101/2024.11.26.625424

    Figure Lengend Snippet: a . Left: total cell number in E3.5 embryos (X m Y n=57, X m X p n= 31, X p O=10, X p O Xist Δ n= 14 embryos); mean value indicated by a red diamond; p -value generated using Student’s t-test. Right: Z-projection of confocal sections (1µm thickness) of E3.5 embryos stained for CDX2 (outside cells), and NANOG (inside cells); scale bar: 20µm. b . UMAP showing E3.5 X p O (blue) and X p O Xist Δ (magenta) cells relative to all other genotypes at E3.5 (green) and other time points (grey). c . Proportion of cells within each cluster (uncommitted, ICM, TE) per genotype at E3.5, derived from UMAP in b . d . Normalised expression of early ( Cdx2 ) and late ( Eomes , Elf5 ) TE genes in E3.5 TE cluster cells. e . X-to-autosome (X:A) ratios of X p O and X p O Xist Δ embryos; P values derived from Student’s t-test; one point was excluded as it is outside the represented range. f . Left: quantitation of inactive X-associated ubiquitylated histone H2A at lysine-119 (uH2A) staining in E3.5 embryos (X m Y n=12, X m X p n=10, X p O n=4 embryos); mean value indicated by a red diamond. Right: Z-projection of confocal sections (1µm thickness – total thickness of 10 and 4.5µm respectively) of E3.5 embryos showing uH2A staining. Presence and absence of inactive X-associated uH2A shown by magenta and white circles, respectively. Inserts show a representative image of cells without and with a uH2A cloud. g . E10.5 embryo weights in mg (log 10 ) by genotypes; mean value indicated by a red diamond; P values derived from Wilcoxon test.

    Article Snippet: Primary antibodies used in this study were: rabbit anti-H2AK119ub1 (Cell Signaling, 8240, 1:500), rabbit anti-Nanog (Cosmo Bio, RCAB001P, 1:500), goat anti-Cdx2 (R&D Systems, AF3665-SP, 1:500).

    Techniques: Generated, Staining, Derivative Assay, Expressing, Quantitation Assay