human pdgf r beta antibody Search Results


goat anti pdgfrβ  (R&D Systems)
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human pdgfrβ biotinylated antibody  (R&D Systems)
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fab1263t 100ug  (R&D Systems)
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ms r d systems mab1263 lc3b 122 000 rb novus nb100  (R&D Systems)
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tube 2 mouse anti human pdgfrβ pe fab1263p r d systems  (R&D Systems)
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pdgfrb  (R&D Systems)
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anti human pdgfr β  (R&D Systems)
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r d systems cat fab1263a  (R&D Systems)
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cd140b fitc fab1263f  (R&D Systems)
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pdgfrβ  (R&D Systems)
91
R&D Systems pdgfrβ
1m treatment induces differentiation towards definitive endoderm. Shef-3 hESCs were cultured for a total of 7 days, feeder-free on Matrigel, in chemically defined mTeSR1 medium with 2 μM 1m included in the medium for the number of days indicated (0d, hESCs cultured for 7 days without 1m). ( A ) RT-PCR analyses were performed using primers selective for the genes specified. ( B ) Shef-3 hESCs cultured under the conditions indicated for the duration of the experiment in Lumox 24-well trays were analysed by immunofluorescence for expression <t>of</t> <t>brachyury,</t> <t>PDGFRβ,</t> FOXA2, SOX17 and HNF4α. Cells were counterstained with DAPI for nuclear localization and the lower panels show the superimposed images. Scale bars: 50 μm. DMSO controls were cultured for the entire 7-day period.
Pdgfrβ, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pdgfrb r d systems  (R&D Systems)
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1m treatment induces differentiation towards definitive endoderm. Shef-3 hESCs were cultured for a total of 7 days, feeder-free on Matrigel, in chemically defined mTeSR1 medium with 2 μM 1m included in the medium for the number of days indicated (0d, hESCs cultured for 7 days without 1m). ( A ) RT-PCR analyses were performed using primers selective for the genes specified. ( B ) Shef-3 hESCs cultured under the conditions indicated for the duration of the experiment in Lumox 24-well trays were analysed by immunofluorescence for expression <t>of</t> <t>brachyury,</t> <t>PDGFRβ,</t> FOXA2, SOX17 and HNF4α. Cells were counterstained with DAPI for nuclear localization and the lower panels show the superimposed images. Scale bars: 50 μm. DMSO controls were cultured for the entire 7-day period.
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anti human platelet derived growth factor receptor beta  (R&D Systems)
93
R&D Systems anti human platelet derived growth factor receptor beta
1m treatment induces differentiation towards definitive endoderm. Shef-3 hESCs were cultured for a total of 7 days, feeder-free on Matrigel, in chemically defined mTeSR1 medium with 2 μM 1m included in the medium for the number of days indicated (0d, hESCs cultured for 7 days without 1m). ( A ) RT-PCR analyses were performed using primers selective for the genes specified. ( B ) Shef-3 hESCs cultured under the conditions indicated for the duration of the experiment in Lumox 24-well trays were analysed by immunofluorescence for expression <t>of</t> <t>brachyury,</t> <t>PDGFRβ,</t> FOXA2, SOX17 and HNF4α. Cells were counterstained with DAPI for nuclear localization and the lower panels show the superimposed images. Scale bars: 50 μm. DMSO controls were cultured for the entire 7-day period.
Anti Human Platelet Derived Growth Factor Receptor Beta, supplied by R&D Systems, 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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anti human platelet derived growth factor receptor beta - by Bioz Stars, 2026-09
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Image Search Results


1m treatment induces differentiation towards definitive endoderm. Shef-3 hESCs were cultured for a total of 7 days, feeder-free on Matrigel, in chemically defined mTeSR1 medium with 2 μM 1m included in the medium for the number of days indicated (0d, hESCs cultured for 7 days without 1m). ( A ) RT-PCR analyses were performed using primers selective for the genes specified. ( B ) Shef-3 hESCs cultured under the conditions indicated for the duration of the experiment in Lumox 24-well trays were analysed by immunofluorescence for expression of brachyury, PDGFRβ, FOXA2, SOX17 and HNF4α. Cells were counterstained with DAPI for nuclear localization and the lower panels show the superimposed images. Scale bars: 50 μm. DMSO controls were cultured for the entire 7-day period.

Journal: Journal of Cell Science

Article Title: A novel chemically directed route for the generation of definitive endoderm from human embryonic stem cells based on inhibition of GSK-3

doi: 10.1242/jcs.081679

Figure Lengend Snippet: 1m treatment induces differentiation towards definitive endoderm. Shef-3 hESCs were cultured for a total of 7 days, feeder-free on Matrigel, in chemically defined mTeSR1 medium with 2 μM 1m included in the medium for the number of days indicated (0d, hESCs cultured for 7 days without 1m). ( A ) RT-PCR analyses were performed using primers selective for the genes specified. ( B ) Shef-3 hESCs cultured under the conditions indicated for the duration of the experiment in Lumox 24-well trays were analysed by immunofluorescence for expression of brachyury, PDGFRβ, FOXA2, SOX17 and HNF4α. Cells were counterstained with DAPI for nuclear localization and the lower panels show the superimposed images. Scale bars: 50 μm. DMSO controls were cultured for the entire 7-day period.

Article Snippet: Antibodies against the following proteins were used: brachyury (4 μg/ml, goat; AF2085, R&D Systems), PDGFRβ (5 μg/ml, mouse; MAB385, R&D Systems), FOXA2 (5 μg/ml, goat; AF2400, R&D Systems), SOX17 (5 μg/ml, goat; AF1924, R&D Systems), HNF4α (2 μg/ml, rabbit; sc-8987, Santa Cruz Biotechnology), AFP (1:100, rabbit; A0008, DAKO), and TTR (1:100, rabbit; A0002 DAKO).

Techniques: Cell Culture, Reverse Transcription Polymerase Chain Reaction, Immunofluorescence, Expressing