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Biogenex mouse anti-cdx2 mu392a-uc
Mouse Anti Cdx2 Mu392a Uc, supplied by Biogenex, 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-cdx2+mu392a-uc/cdx2+antibody/bio_rxiv__2025__07__07__663418-152-4-6
Average 90 stars, based on 1 article reviews
mouse anti-cdx2 mu392a-uc - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Derivative Assay:

Article Title: Loss of RBBP4 results in defective inner cell mass, severe apoptosis, hyperacetylated histones and preimplantation lethality in mice
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC), rabbit anti-NANOG (Abcam, ab80892), rabbit anti-TRP53 (Cell Signaling Technology, #9284), rabbit anti-RBBP4 (Abcam, ab79416), rabbit anti-H4 (acetyl K5 + K8 + K12 + K16) (Abcam, ab177790), rabbit anti-H3 (acetyl K56) (Abcam, ab76307), rabbit anti-H3K27me3 (Millipore, 07-449), goat anti-SOX17 (R&D Systems, AF1924), and goat anti-OCT4 (Abcam, ab27985).

Article Title: Vitrification of Pronuclear Zygotes Perturbs Porcine Zygotic Genome Activation
Article Snippet: Blastocysts were fixed in 4% paraformaldehyde solution for 24 h, permeabilized with 0.5% Triton X-100 for 30 min, and then blocked with 2% BSA for 1 h. Blastocysts were incubated in primary antibodies (mouse anti-CDX2 (MU392A-UC, Biogenex, Fremont, CA, USA)) overnight at 4 °C.

Article Title: MCRS1 is essential for epiblast development during early mouse embryogenesis
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC); rabbit anti-NANOG (Abcam, ab80892); rabbit anti-TRP53 (Cell Signaling Technology, #9284); rabbit anti-MCRS1 (Sigma-Aldrich, HPA039057); rabbit anti-H4K5 + K8 + K12 + K16 (Abcam, ab177790); goat anti-SOX17 (R&D Systems, AF1924); goat anti-OCT4 (Abcam, ab27985).

Article Title: Stage- and tissue-specific gene editing using 4-OHT inducible Cas9 in whole organism
Article Snippet: The primary antibodies included mouse anti-Cdx2 (BioGenex, MU392A-UC, 1:200 dilution), rabbit anti-Nanog (Abcam, Ab214549, 1:100 dilution), and rabbit anti-mCherry (Easybio, BE2027, 1:200 dilution).

Article Title: Early embryonic lethality of mice lacking POLD2.
Article Snippet: Anhui Province Key Laboratory of Embryo Development and Reproductive Regulation, Anhui Province Key Laboratory of Environmental Hormone and Reproduction, Fuyang Normal University, Fuyang, Anhui, China Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA Animal Models Core Facility, Institute for Applied Life Sciences (IALS), University of Massachusetts, Amherst, Massachusetts, USA

Article Title: Mesenchymal-epithelial interaction regulates gastrointestinal tract development in mouse embryos.
Article Snippet: In brief Based on single-cell and spatial RNA sequencing, Zhao et al. depict a comprehensive transcriptomic landscape of the developing mouse stomach and small and large intestine during E9.5–E15.5.. This landscape reveals a dynamic cell atlas, uncovers the early regionalization process, and reveals mesenchymal-epithelial interactions regulating critical developmental events and cell fate determination.

Article Title: The RNA m 6 A reader YTHDC1 silences retrotransposons and guards ES cell identity.
Article Snippet: The RNA modification N-methyladenosine (mA) has critical roles in many biological processes.. However, the function of mA in the early phase of mammalian development remains poorly understood.. Here we show that the mA reader YT521-B homology-domain-containing protein 1 (YTHDC1) is required for the maintenance of mouse embryonic stem (ES) cells in an mA-dependent manner, and that its deletion initiates cellular reprogramming to a 2C-like state.

Article Title: Induction of mouse totipotent stem cells by a defined chemical cocktail.
Article Snippet: In mice, only the zygotes and blastomeres from 2-cell embryos are authentic totipotent stem cells (TotiSCs) capable of producing all the differentiated cells in both embryonic and extraembryonic tissues and forming an entire organism.. However, it remains unknown whether and how totipotent stem cells can be established in vitro in the absence of germline cells.. Here we demonstrate the induction and long-term maintenance of TotiSCs from mouse pluripotent stem cells using a combination of three small molecules: the retinoic acid analogue TTNPB, 1-azakenpaullone and the kinase blocker WS6.

Incubation:

Article Title: Loss of RBBP4 results in defective inner cell mass, severe apoptosis, hyperacetylated histones and preimplantation lethality in mice
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC), rabbit anti-NANOG (Abcam, ab80892), rabbit anti-TRP53 (Cell Signaling Technology, #9284), rabbit anti-RBBP4 (Abcam, ab79416), rabbit anti-H4 (acetyl K5 + K8 + K12 + K16) (Abcam, ab177790), rabbit anti-H3 (acetyl K56) (Abcam, ab76307), rabbit anti-H3K27me3 (Millipore, 07-449), goat anti-SOX17 (R&D Systems, AF1924), and goat anti-OCT4 (Abcam, ab27985).

Article Title: Vitrification of Pronuclear Zygotes Perturbs Porcine Zygotic Genome Activation
Article Snippet: Blastocysts were fixed in 4% paraformaldehyde solution for 24 h, permeabilized with 0.5% Triton X-100 for 30 min, and then blocked with 2% BSA for 1 h. Blastocysts were incubated in primary antibodies (mouse anti-CDX2 (MU392A-UC, Biogenex, Fremont, CA, USA)) overnight at 4 °C.

Article Title: MCRS1 is essential for epiblast development during early mouse embryogenesis
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC); rabbit anti-NANOG (Abcam, ab80892); rabbit anti-TRP53 (Cell Signaling Technology, #9284); rabbit anti-MCRS1 (Sigma-Aldrich, HPA039057); rabbit anti-H4K5 + K8 + K12 + K16 (Abcam, ab177790); goat anti-SOX17 (R&D Systems, AF1924); goat anti-OCT4 (Abcam, ab27985).

Article Title: Stage- and tissue-specific gene editing using 4-OHT inducible Cas9 in whole organism
Article Snippet: The primary antibodies included mouse anti-Cdx2 (BioGenex, MU392A-UC, 1:200 dilution), rabbit anti-Nanog (Abcam, Ab214549, 1:100 dilution), and rabbit anti-mCherry (Easybio, BE2027, 1:200 dilution).

Article Title: Early embryonic lethality of mice lacking POLD2.
Article Snippet: Anhui Province Key Laboratory of Embryo Development and Reproductive Regulation, Anhui Province Key Laboratory of Environmental Hormone and Reproduction, Fuyang Normal University, Fuyang, Anhui, China Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA Animal Models Core Facility, Institute for Applied Life Sciences (IALS), University of Massachusetts, Amherst, Massachusetts, USA

Article Title: Mesenchymal-epithelial interaction regulates gastrointestinal tract development in mouse embryos.
Article Snippet: In brief Based on single-cell and spatial RNA sequencing, Zhao et al. depict a comprehensive transcriptomic landscape of the developing mouse stomach and small and large intestine during E9.5–E15.5.. This landscape reveals a dynamic cell atlas, uncovers the early regionalization process, and reveals mesenchymal-epithelial interactions regulating critical developmental events and cell fate determination.

Article Title: The RNA m 6 A reader YTHDC1 silences retrotransposons and guards ES cell identity.
Article Snippet: The RNA modification N-methyladenosine (mA) has critical roles in many biological processes.. However, the function of mA in the early phase of mammalian development remains poorly understood.. Here we show that the mA reader YT521-B homology-domain-containing protein 1 (YTHDC1) is required for the maintenance of mouse embryonic stem (ES) cells in an mA-dependent manner, and that its deletion initiates cellular reprogramming to a 2C-like state.

Article Title: Induction of mouse totipotent stem cells by a defined chemical cocktail.
Article Snippet: In mice, only the zygotes and blastomeres from 2-cell embryos are authentic totipotent stem cells (TotiSCs) capable of producing all the differentiated cells in both embryonic and extraembryonic tissues and forming an entire organism.. However, it remains unknown whether and how totipotent stem cells can be established in vitro in the absence of germline cells.. Here we demonstrate the induction and long-term maintenance of TotiSCs from mouse pluripotent stem cells using a combination of three small molecules: the retinoic acid analogue TTNPB, 1-azakenpaullone and the kinase blocker WS6.

Staining:

Article Title: Loss of RBBP4 results in defective inner cell mass, severe apoptosis, hyperacetylated histones and preimplantation lethality in mice
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC), rabbit anti-NANOG (Abcam, ab80892), rabbit anti-TRP53 (Cell Signaling Technology, #9284), rabbit anti-RBBP4 (Abcam, ab79416), rabbit anti-H4 (acetyl K5 + K8 + K12 + K16) (Abcam, ab177790), rabbit anti-H3 (acetyl K56) (Abcam, ab76307), rabbit anti-H3K27me3 (Millipore, 07-449), goat anti-SOX17 (R&D Systems, AF1924), and goat anti-OCT4 (Abcam, ab27985).

Article Title: Vitrification of Pronuclear Zygotes Perturbs Porcine Zygotic Genome Activation
Article Snippet: Blastocysts were fixed in 4% paraformaldehyde solution for 24 h, permeabilized with 0.5% Triton X-100 for 30 min, and then blocked with 2% BSA for 1 h. Blastocysts were incubated in primary antibodies (mouse anti-CDX2 (MU392A-UC, Biogenex, Fremont, CA, USA)) overnight at 4 °C.

Article Title: MCRS1 is essential for epiblast development during early mouse embryogenesis
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC); rabbit anti-NANOG (Abcam, ab80892); rabbit anti-TRP53 (Cell Signaling Technology, #9284); rabbit anti-MCRS1 (Sigma-Aldrich, HPA039057); rabbit anti-H4K5 + K8 + K12 + K16 (Abcam, ab177790); goat anti-SOX17 (R&D Systems, AF1924); goat anti-OCT4 (Abcam, ab27985).

Article Title: Stage- and tissue-specific gene editing using 4-OHT inducible Cas9 in whole organism
Article Snippet: The primary antibodies included mouse anti-Cdx2 (BioGenex, MU392A-UC, 1:200 dilution), rabbit anti-Nanog (Abcam, Ab214549, 1:100 dilution), and rabbit anti-mCherry (Easybio, BE2027, 1:200 dilution).

Article Title: Early embryonic lethality of mice lacking POLD2.
Article Snippet: Anhui Province Key Laboratory of Embryo Development and Reproductive Regulation, Anhui Province Key Laboratory of Environmental Hormone and Reproduction, Fuyang Normal University, Fuyang, Anhui, China Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA Animal Models Core Facility, Institute for Applied Life Sciences (IALS), University of Massachusetts, Amherst, Massachusetts, USA

Article Title: Mesenchymal-epithelial interaction regulates gastrointestinal tract development in mouse embryos.
Article Snippet: In brief Based on single-cell and spatial RNA sequencing, Zhao et al. depict a comprehensive transcriptomic landscape of the developing mouse stomach and small and large intestine during E9.5–E15.5.. This landscape reveals a dynamic cell atlas, uncovers the early regionalization process, and reveals mesenchymal-epithelial interactions regulating critical developmental events and cell fate determination.

Article Title: The RNA m 6 A reader YTHDC1 silences retrotransposons and guards ES cell identity.
Article Snippet: The RNA modification N-methyladenosine (mA) has critical roles in many biological processes.. However, the function of mA in the early phase of mammalian development remains poorly understood.. Here we show that the mA reader YT521-B homology-domain-containing protein 1 (YTHDC1) is required for the maintenance of mouse embryonic stem (ES) cells in an mA-dependent manner, and that its deletion initiates cellular reprogramming to a 2C-like state.

Article Title: Induction of mouse totipotent stem cells by a defined chemical cocktail.
Article Snippet: In mice, only the zygotes and blastomeres from 2-cell embryos are authentic totipotent stem cells (TotiSCs) capable of producing all the differentiated cells in both embryonic and extraembryonic tissues and forming an entire organism.. However, it remains unknown whether and how totipotent stem cells can be established in vitro in the absence of germline cells.. Here we demonstrate the induction and long-term maintenance of TotiSCs from mouse pluripotent stem cells using a combination of three small molecules: the retinoic acid analogue TTNPB, 1-azakenpaullone and the kinase blocker WS6.

Control:

Article Title: Loss of RBBP4 results in defective inner cell mass, severe apoptosis, hyperacetylated histones and preimplantation lethality in mice
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC), rabbit anti-NANOG (Abcam, ab80892), rabbit anti-TRP53 (Cell Signaling Technology, #9284), rabbit anti-RBBP4 (Abcam, ab79416), rabbit anti-H4 (acetyl K5 + K8 + K12 + K16) (Abcam, ab177790), rabbit anti-H3 (acetyl K56) (Abcam, ab76307), rabbit anti-H3K27me3 (Millipore, 07-449), goat anti-SOX17 (R&D Systems, AF1924), and goat anti-OCT4 (Abcam, ab27985).

Article Title: Vitrification of Pronuclear Zygotes Perturbs Porcine Zygotic Genome Activation
Article Snippet: Blastocysts were fixed in 4% paraformaldehyde solution for 24 h, permeabilized with 0.5% Triton X-100 for 30 min, and then blocked with 2% BSA for 1 h. Blastocysts were incubated in primary antibodies (mouse anti-CDX2 (MU392A-UC, Biogenex, Fremont, CA, USA)) overnight at 4 °C.

Article Title: MCRS1 is essential for epiblast development during early mouse embryogenesis
Article Snippet: All primary antibodies for IF were used at 1:200 including mouse anti-CDX2 (BioGenex, MU392A-UC); rabbit anti-NANOG (Abcam, ab80892); rabbit anti-TRP53 (Cell Signaling Technology, #9284); rabbit anti-MCRS1 (Sigma-Aldrich, HPA039057); rabbit anti-H4K5 + K8 + K12 + K16 (Abcam, ab177790); goat anti-SOX17 (R&D Systems, AF1924); goat anti-OCT4 (Abcam, ab27985).

Article Title: Stage- and tissue-specific gene editing using 4-OHT inducible Cas9 in whole organism
Article Snippet: The primary antibodies included mouse anti-Cdx2 (BioGenex, MU392A-UC, 1:200 dilution), rabbit anti-Nanog (Abcam, Ab214549, 1:100 dilution), and rabbit anti-mCherry (Easybio, BE2027, 1:200 dilution).

Article Title: Early embryonic lethality of mice lacking POLD2.
Article Snippet: Anhui Province Key Laboratory of Embryo Development and Reproductive Regulation, Anhui Province Key Laboratory of Environmental Hormone and Reproduction, Fuyang Normal University, Fuyang, Anhui, China Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA Animal Models Core Facility, Institute for Applied Life Sciences (IALS), University of Massachusetts, Amherst, Massachusetts, USA

Article Title: Mesenchymal-epithelial interaction regulates gastrointestinal tract development in mouse embryos.
Article Snippet: In brief Based on single-cell and spatial RNA sequencing, Zhao et al. depict a comprehensive transcriptomic landscape of the developing mouse stomach and small and large intestine during E9.5–E15.5.. This landscape reveals a dynamic cell atlas, uncovers the early regionalization process, and reveals mesenchymal-epithelial interactions regulating critical developmental events and cell fate determination.

Article Title: The RNA m 6 A reader YTHDC1 silences retrotransposons and guards ES cell identity.
Article Snippet: The RNA modification N-methyladenosine (mA) has critical roles in many biological processes.. However, the function of mA in the early phase of mammalian development remains poorly understood.. Here we show that the mA reader YT521-B homology-domain-containing protein 1 (YTHDC1) is required for the maintenance of mouse embryonic stem (ES) cells in an mA-dependent manner, and that its deletion initiates cellular reprogramming to a 2C-like state.

Article Title: Induction of mouse totipotent stem cells by a defined chemical cocktail.
Article Snippet: In mice, only the zygotes and blastomeres from 2-cell embryos are authentic totipotent stem cells (TotiSCs) capable of producing all the differentiated cells in both embryonic and extraembryonic tissues and forming an entire organism.. However, it remains unknown whether and how totipotent stem cells can be established in vitro in the absence of germline cells.. Here we demonstrate the induction and long-term maintenance of TotiSCs from mouse pluripotent stem cells using a combination of three small molecules: the retinoic acid analogue TTNPB, 1-azakenpaullone and the kinase blocker WS6.



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The quality of blastocysts developed in microgravity on the ISS (A–D) ICM and TE cells were immunostained using Nanog and <t>Cdx2</t> antibodies, respectively. The blastocysts were obtained from ETCs cultured on the ground (A), artificial-1 g (B), and μ g (C, D) on the ISS. One blastocyst from μ g showing ectopic expression of NANOG (D). Nanog-positive cells (ICM) are in red, and CDX2-positive cells (TE) are in green. All images are shown by z stack, except (D). The numbers of ICM cells (red bar), TE cells (green bar), and the total cell (blue) are shown in (I). Data are represented as mean ± SEM. (E–H) γ-H2A.x-positive cells and ICM cells were immunostained. Blastocysts were obtained same as above. (H) A blastocyst with ectopic expression of NANOG. Embryonic nuclei were detected using DAPI (blue). Nanog-positive cells are in red, and γ-H2A.x-positive cells are in green. (J) The rate of blastocysts with ectopic expression of NANOG was compared between 1 g control cultured in a dish (n = 135), ETC on Earth (n = 146), artificial-1 g (n = 12), and μ g (n = 9) on the ISS. (K) Principal-component analysis of expression profiles of 5 blastocysts for each of the three experimental groups, μ g, a-1 g, and ground, was analyzed by RNA-seq. No separation was observed in principa components 1 and 2. Individual blastocysts are in brown: ground; pink: artificial-1 g; and blue: μ g.
Anti Cdx2 Mouse Monoclonal Antibody Mu392a Uc, supplied by Biogenex, 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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Biogenex mouse monoclonal anti-mouse cdx2 mu392a-uc
The quality of blastocysts developed in microgravity on the ISS (A–D) ICM and TE cells were immunostained using Nanog and <t>Cdx2</t> antibodies, respectively. The blastocysts were obtained from ETCs cultured on the ground (A), artificial-1 g (B), and μ g (C, D) on the ISS. One blastocyst from μ g showing ectopic expression of NANOG (D). Nanog-positive cells (ICM) are in red, and CDX2-positive cells (TE) are in green. All images are shown by z stack, except (D). The numbers of ICM cells (red bar), TE cells (green bar), and the total cell (blue) are shown in (I). Data are represented as mean ± SEM. (E–H) γ-H2A.x-positive cells and ICM cells were immunostained. Blastocysts were obtained same as above. (H) A blastocyst with ectopic expression of NANOG. Embryonic nuclei were detected using DAPI (blue). Nanog-positive cells are in red, and γ-H2A.x-positive cells are in green. (J) The rate of blastocysts with ectopic expression of NANOG was compared between 1 g control cultured in a dish (n = 135), ETC on Earth (n = 146), artificial-1 g (n = 12), and μ g (n = 9) on the ISS. (K) Principal-component analysis of expression profiles of 5 blastocysts for each of the three experimental groups, μ g, a-1 g, and ground, was analyzed by RNA-seq. No separation was observed in principa components 1 and 2. Individual blastocysts are in brown: ground; pink: artificial-1 g; and blue: μ g.
Mouse Monoclonal Anti Mouse Cdx2 Mu392a Uc, supplied by Biogenex, 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-cdx2+mu392a-uc/cdx2+antibody/pmc09492771__41467_2022_32481_MOESM6_ESM-65-66-71
Average 90 stars, based on 1 article reviews
mouse monoclonal anti-mouse cdx2 mu392a-uc - by Bioz Stars, 2026-10
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Image Search Results


The quality of blastocysts developed in microgravity on the ISS (A–D) ICM and TE cells were immunostained using Nanog and Cdx2 antibodies, respectively. The blastocysts were obtained from ETCs cultured on the ground (A), artificial-1 g (B), and μ g (C, D) on the ISS. One blastocyst from μ g showing ectopic expression of NANOG (D). Nanog-positive cells (ICM) are in red, and CDX2-positive cells (TE) are in green. All images are shown by z stack, except (D). The numbers of ICM cells (red bar), TE cells (green bar), and the total cell (blue) are shown in (I). Data are represented as mean ± SEM. (E–H) γ-H2A.x-positive cells and ICM cells were immunostained. Blastocysts were obtained same as above. (H) A blastocyst with ectopic expression of NANOG. Embryonic nuclei were detected using DAPI (blue). Nanog-positive cells are in red, and γ-H2A.x-positive cells are in green. (J) The rate of blastocysts with ectopic expression of NANOG was compared between 1 g control cultured in a dish (n = 135), ETC on Earth (n = 146), artificial-1 g (n = 12), and μ g (n = 9) on the ISS. (K) Principal-component analysis of expression profiles of 5 blastocysts for each of the three experimental groups, μ g, a-1 g, and ground, was analyzed by RNA-seq. No separation was observed in principa components 1 and 2. Individual blastocysts are in brown: ground; pink: artificial-1 g; and blue: μ g.

Journal: iScience

Article Title: Effect of microgravity on mammalian embryo development evaluated at the International Space Station

doi: 10.1016/j.isci.2023.108177

Figure Lengend Snippet: The quality of blastocysts developed in microgravity on the ISS (A–D) ICM and TE cells were immunostained using Nanog and Cdx2 antibodies, respectively. The blastocysts were obtained from ETCs cultured on the ground (A), artificial-1 g (B), and μ g (C, D) on the ISS. One blastocyst from μ g showing ectopic expression of NANOG (D). Nanog-positive cells (ICM) are in red, and CDX2-positive cells (TE) are in green. All images are shown by z stack, except (D). The numbers of ICM cells (red bar), TE cells (green bar), and the total cell (blue) are shown in (I). Data are represented as mean ± SEM. (E–H) γ-H2A.x-positive cells and ICM cells were immunostained. Blastocysts were obtained same as above. (H) A blastocyst with ectopic expression of NANOG. Embryonic nuclei were detected using DAPI (blue). Nanog-positive cells are in red, and γ-H2A.x-positive cells are in green. (J) The rate of blastocysts with ectopic expression of NANOG was compared between 1 g control cultured in a dish (n = 135), ETC on Earth (n = 146), artificial-1 g (n = 12), and μ g (n = 9) on the ISS. (K) Principal-component analysis of expression profiles of 5 blastocysts for each of the three experimental groups, μ g, a-1 g, and ground, was analyzed by RNA-seq. No separation was observed in principa components 1 and 2. Individual blastocysts are in brown: ground; pink: artificial-1 g; and blue: μ g.

Article Snippet: The anti-CDX2 mouse monoclonal antibody (1:500; BioGenex, San Ramon, CA, USA, MU392A-UC) to detect TE cells and anti-Nanog rabbit polyclonal antibody (1:500; Abcam, Cambridge, UK, ab80892) to detect the ICM cells were the primary antibodies used.

Techniques: Cell Culture, Expressing, Control, RNA Sequencing

Journal: iScience

Article Title: Effect of microgravity on mammalian embryo development evaluated at the International Space Station

doi: 10.1016/j.isci.2023.108177

Figure Lengend Snippet:

Article Snippet: The anti-CDX2 mouse monoclonal antibody (1:500; BioGenex, San Ramon, CA, USA, MU392A-UC) to detect TE cells and anti-Nanog rabbit polyclonal antibody (1:500; Abcam, Cambridge, UK, ab80892) to detect the ICM cells were the primary antibodies used.

Techniques: Recombinant, Isolation, Software, Sequencing