goat anti mouse igm bound cd90 Search Results


92
Revvity pe mouse igg1
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Jackson Immuno goat anti rat cy2 thy1 2 antibodies
Goat Anti Rat Cy2 Thy1 2 Antibodies, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Danaher Inc mouse anti thy1
Primer sequences for the RT-PCR and q-PCR analyses
Mouse Anti Thy1, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad goat anti mouse igm bound cd90
Primer sequences for the RT-PCR and q-PCR analyses
Goat Anti Mouse Igm Bound Cd90, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Novus Biologicals nbp2 37330
Primary antibodies DOI: http://dx.doi.org/10.7554/eLife.26575.041
Nbp2 37330, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc thy1 cst 13801
Primary antibodies DOI: http://dx.doi.org/10.7554/eLife.26575.041
Thy1 Cst 13801, supplied by Cell Signaling Technology Inc, 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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Danaher Inc mouse anti rat monoclonal antibody thy1 1
Identification and purity testing of retinal ganglion cells. Green is <t>Thy1.1</t> immunofluorescence staining and blue is DAPI staining (magnification, ×100 and ×200).
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Danaher Inc cd90
Pericardial effusion-derived progenitor cells (PEPCs) expressed vascular differentiation surface markers at day-14 after implantation on a decellularized porcine pulmonary artery. First row showed positive control of CD105 (green) and <t>CD90</t> (red) expressions on HUVECs after implanting the cells on the intimal surface at day-14. PEPCs grew and migrated better when implanted on the adventitia surface (second row) as compared with implantation on intimal (the 3rd row) and lateral surfaces (the 4th row). All PEPCs expressed CD105 and CD90 after implantation. arrows indicated cells merged with all markers. Bar = 50 µm.
Cd90, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology cd90
Pericardial effusion-derived progenitor cells (PEPCs) expressed vascular differentiation surface markers at day-14 after implantation on a decellularized porcine pulmonary artery. First row showed positive control of CD105 (green) and <t>CD90</t> (red) expressions on HUVECs after implanting the cells on the intimal surface at day-14. PEPCs grew and migrated better when implanted on the adventitia surface (second row) as compared with implantation on intimal (the 3rd row) and lateral surfaces (the 4th row). All PEPCs expressed CD105 and CD90 after implantation. arrows indicated cells merged with all markers. Bar = 50 µm.
Cd90, supplied by Santa Cruz Biotechnology, 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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93
Bio-Rad thy 1
Antibodies used
Thy 1, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
OriGene goat anti human cd90 thy1 antibody
Antibodies used
Goat Anti Human Cd90 Thy1 Antibody, supplied by OriGene, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cd90  (Bioss)
93
Bioss cd90
Primer sequences used in this study
Cd90, supplied by Bioss, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Primer sequences for the RT-PCR and q-PCR analyses

Journal: Journal of Animal Science and Biotechnology

Article Title: Establishment of cell lines with porcine spermatogonial stem cell properties

doi: 10.1186/s40104-020-00439-0

Figure Lengend Snippet: Primer sequences for the RT-PCR and q-PCR analyses

Article Snippet: The primary antibodies used were mouse anti-UCHL1 (1: 1,000; ab8189, Abcam), rabbit anti-PLZF (1: 1,000; ab104854, Abcam), mouse anti-THY1 (1: 1,000; ab205719, Abcam), rabbit anti-VASA (1: 1,000; ab13840, Abcam), rabbit anti-DAZL (1: 500; ab34139, Abcam), goat anti-CXCR4 (1: 500; ab1670, Abcam), rabbit anti-SV40 (1: 1,000; 15,729, Cell Signaling Technology), mouse anti-PCNA (1: 1,000; sc-56, Santa Cruz Biotechnology), mouse anti-β-actin (1: 3,000; CW0096, CWBIO), rabbit anti-KIT (1: 1,000; 3074, Cell Signaling Technology) and rabbit anti-STRA8 (1: 1,000; ab49602, Abcam).

Techniques:

Characterization of immortalized porcine SSCs. a RT-PCR assay showing the transcripts of UCHL1 , PLZF , THY1 , VASA , DAZL , CXCR4 , SV40 and PCNA in the immortalized SSCs from passage 4 (P4) to passage 12 (P12). The RNAs from 7-day-old porcine testes are used as controls, and GAPDH serves as a loading control. -RT: the negative control omitting reverse transcription but with PCR reaction. b Western blot assay showing the protein expression of UCHL1, THY1, SV40, PCNA, PLZF, VASA, DAZL and CXCR4 in the immortalized SSCs at different passages. The protein extracts from 7-day-old porcine testes are used as controls, and β-actin serves as a loading control. c Staining of Ttag-transduced SSCs (passage 20) on cytospin slides for UCHL1, PLZF, VASA, DAZL, CXCR4, SV40 and PCNA. NC: the negative control using the isotype IgG in place of the primary antibody. Bar = 50 μm

Journal: Journal of Animal Science and Biotechnology

Article Title: Establishment of cell lines with porcine spermatogonial stem cell properties

doi: 10.1186/s40104-020-00439-0

Figure Lengend Snippet: Characterization of immortalized porcine SSCs. a RT-PCR assay showing the transcripts of UCHL1 , PLZF , THY1 , VASA , DAZL , CXCR4 , SV40 and PCNA in the immortalized SSCs from passage 4 (P4) to passage 12 (P12). The RNAs from 7-day-old porcine testes are used as controls, and GAPDH serves as a loading control. -RT: the negative control omitting reverse transcription but with PCR reaction. b Western blot assay showing the protein expression of UCHL1, THY1, SV40, PCNA, PLZF, VASA, DAZL and CXCR4 in the immortalized SSCs at different passages. The protein extracts from 7-day-old porcine testes are used as controls, and β-actin serves as a loading control. c Staining of Ttag-transduced SSCs (passage 20) on cytospin slides for UCHL1, PLZF, VASA, DAZL, CXCR4, SV40 and PCNA. NC: the negative control using the isotype IgG in place of the primary antibody. Bar = 50 μm

Article Snippet: The primary antibodies used were mouse anti-UCHL1 (1: 1,000; ab8189, Abcam), rabbit anti-PLZF (1: 1,000; ab104854, Abcam), mouse anti-THY1 (1: 1,000; ab205719, Abcam), rabbit anti-VASA (1: 1,000; ab13840, Abcam), rabbit anti-DAZL (1: 500; ab34139, Abcam), goat anti-CXCR4 (1: 500; ab1670, Abcam), rabbit anti-SV40 (1: 1,000; 15,729, Cell Signaling Technology), mouse anti-PCNA (1: 1,000; sc-56, Santa Cruz Biotechnology), mouse anti-β-actin (1: 3,000; CW0096, CWBIO), rabbit anti-KIT (1: 1,000; 3074, Cell Signaling Technology) and rabbit anti-STRA8 (1: 1,000; ab49602, Abcam).

Techniques: Reverse Transcription Polymerase Chain Reaction, Negative Control, Western Blot, Expressing, Staining

Primary antibodies DOI: http://dx.doi.org/10.7554/eLife.26575.041

Journal: eLife

Article Title: Human embryonic lung epithelial tips are multipotent progenitors that can be expanded in vitro as long-term self-renewing organoids

doi: 10.7554/eLife.26575

Figure Lengend Snippet: Primary antibodies DOI: http://dx.doi.org/10.7554/eLife.26575.041

Article Snippet: CD90 , Novus Biologicals, UK , NBP2-37330 (clone 7E1B11) , Mouse , 1:200 , No , N/A , RRID: AB_2665376.

Techniques: Amplification, Transduction

Identification and purity testing of retinal ganglion cells. Green is Thy1.1 immunofluorescence staining and blue is DAPI staining (magnification, ×100 and ×200).

Journal: Molecular Medicine Reports

Article Title: High hydrostatic pressure induces apoptosis of retinal ganglion cells via regulation of the NGF signalling pathway

doi: 10.3892/mmr.2019.10206

Figure Lengend Snippet: Identification and purity testing of retinal ganglion cells. Green is Thy1.1 immunofluorescence staining and blue is DAPI staining (magnification, ×100 and ×200).

Article Snippet: Cells separated from the petri dish wall were transferred to another petri dish coated with HRP-conjugated goat anti-rabbit IgM (1:300; cat no. ab97180; Abcam) and mouse anti-rat monoclonal antibody Thy1.1 (1:100; cat no. ab6721; Abcam) for 30 min at room temperature, following which the cells that separated from the petri dish wall were removed.

Techniques: Immunofluorescence, Staining

Pericardial effusion-derived progenitor cells (PEPCs) expressed vascular differentiation surface markers at day-14 after implantation on a decellularized porcine pulmonary artery. First row showed positive control of CD105 (green) and CD90 (red) expressions on HUVECs after implanting the cells on the intimal surface at day-14. PEPCs grew and migrated better when implanted on the adventitia surface (second row) as compared with implantation on intimal (the 3rd row) and lateral surfaces (the 4th row). All PEPCs expressed CD105 and CD90 after implantation. arrows indicated cells merged with all markers. Bar = 50 µm.

Journal: Organogenesis

Article Title: Potential of Autologous Progenitor Cells and Decellularized Porcine Artery Matrix in Construction of Tissue-engineered Vascular Grafts

doi: 10.1080/15476278.2021.1963603

Figure Lengend Snippet: Pericardial effusion-derived progenitor cells (PEPCs) expressed vascular differentiation surface markers at day-14 after implantation on a decellularized porcine pulmonary artery. First row showed positive control of CD105 (green) and CD90 (red) expressions on HUVECs after implanting the cells on the intimal surface at day-14. PEPCs grew and migrated better when implanted on the adventitia surface (second row) as compared with implantation on intimal (the 3rd row) and lateral surfaces (the 4th row). All PEPCs expressed CD105 and CD90 after implantation. arrows indicated cells merged with all markers. Bar = 50 µm.

Article Snippet: After washing with PBS, the tissue sections were incubated with fluorescent-conjugated secondary antibody (Alexa Fluor® 488 goat anti-rabbit IgG (H + L), ab150077 for CD90 while ab150113 goat anti-mouse IgG (H + L) was applied for CD105, Abcam, Cambridge, UK) for 1 h at room temperature.

Techniques: Derivative Assay, Positive Control

Antibodies used

Journal: Cell Death Discovery

Article Title: Notch signaling in astrocytes mediates their morphological response to an inflammatory challenge

doi: 10.1038/s41420-019-0166-6

Figure Lengend Snippet: Antibodies used

Article Snippet: Thy-1 (against CD90) , Mouse , 1:500 , Bio-Rad (Formerly AbD Serotec).

Techniques:

Primer sequences used in this study

Journal: Stem Cell Research & Therapy

Article Title: Footprint-free induced pluripotent stem cells can be successfully differentiated into mesenchymal stromal cells in the feline model

doi: 10.1186/s13287-025-04325-2

Figure Lengend Snippet: Primer sequences used in this study

Article Snippet: CD90 , primary , polyclonal , rabbit , human , Bioss [bs-0778R] , none , 1:200.

Techniques: Virus

Antibodies used in this study

Journal: Stem Cell Research & Therapy

Article Title: Footprint-free induced pluripotent stem cells can be successfully differentiated into mesenchymal stromal cells in the feline model

doi: 10.1186/s13287-025-04325-2

Figure Lengend Snippet: Antibodies used in this study

Article Snippet: CD90 , primary , polyclonal , rabbit , human , Bioss [bs-0778R] , none , 1:200.

Techniques:

Successful generation of feline iPSC-derived mesenchymal stromal cells (MSCs). ( A ). Morphology of iPSC-derived MSCs-1 and − 2, with evenly distributed plastic adherent cells. ( B ). Conventional RT-PCR analysis of feline MSC-specific surface markers CD29 , CD44 , CD73 , CD90 , and CD105 , the hematopoietic stem cell marker CD34 , and the loading control GAPDH , in feline iPSC-MSCs and iPSCs. Full-length gels are presented in Additional File 10: Fig. . ( C & D ). Immunofluorescence ( C ) and flow cytometric analysis ( D ) of MSC-specific feline surface proteins CD44, CD73, CD90, and CD105 (green). Nuclei were visualized by staining with DAPI (blue)

Journal: Stem Cell Research & Therapy

Article Title: Footprint-free induced pluripotent stem cells can be successfully differentiated into mesenchymal stromal cells in the feline model

doi: 10.1186/s13287-025-04325-2

Figure Lengend Snippet: Successful generation of feline iPSC-derived mesenchymal stromal cells (MSCs). ( A ). Morphology of iPSC-derived MSCs-1 and − 2, with evenly distributed plastic adherent cells. ( B ). Conventional RT-PCR analysis of feline MSC-specific surface markers CD29 , CD44 , CD73 , CD90 , and CD105 , the hematopoietic stem cell marker CD34 , and the loading control GAPDH , in feline iPSC-MSCs and iPSCs. Full-length gels are presented in Additional File 10: Fig. . ( C & D ). Immunofluorescence ( C ) and flow cytometric analysis ( D ) of MSC-specific feline surface proteins CD44, CD73, CD90, and CD105 (green). Nuclei were visualized by staining with DAPI (blue)

Article Snippet: CD90 , primary , polyclonal , rabbit , human , Bioss [bs-0778R] , none , 1:200.

Techniques: Derivative Assay, Reverse Transcription Polymerase Chain Reaction, Marker, Control, Immunofluorescence, Staining