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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
Stemdiff Kit, supplied by STEMCELL Technologies Inc, 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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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
Neural Induction Kit Stemdiff Smadi, supplied by STEMCELL Technologies Inc, 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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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after <t>trilineage</t> differentiation of hiPSC‐lines derived from UDCs.
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Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after trilineage differentiation of hiPSC‐lines derived from UDCs.

Journal: Current Protocols in Stem Cell Biology

Article Title: Reprogramming Urine‐Derived Cells using Commercially Available Self‐Replicative RNA and a Single Electroporation

doi: 10.1002/cpsc.124

Figure Lengend Snippet: Basic characterization of hiPSC lines. ( A ) Use of an immortalized keratinocyte cell‐line (HACAT) as negative control for setting the gates for measuring pluripotency markers. ( B ) Flow cytometry analysis of pluripotency marker expression in UDC‐derived hiPSCs. ( C ) Examples of immunofluorescence staining after trilineage differentiation of hiPSC‐lines derived from UDCs.

Article Snippet: 100% Ethanol Stemdiff Trilineage Differentiation Kit (STEMCELL Technologies, cat. no. 05230) 2% Paraformaldehyde (PFA; see ) Permeabilization/Blocking solution (see ) 4% Normal Swine Serum (4% NSS; see ) Conjugated antibodies (Cell Signaling Technologies, custom‐made, pre‐labeled, see Table ) 0.05% Tween/PBS (see ) DAPI (Invitrogen, cat. no. D3571) MilliQ water ProLong Gold Antifade Mountant (Invitrogen, cat. no. P36930) Glass coverslips (13‐mm diameter) Tweezers Bunsen burner Culture plates (24‐well, sterile, clear) Glass microscope slides (Confocal) Fluorescent microscope

Techniques: Negative Control, Flow Cytometry, Marker, Expressing, Derivative Assay, Immunofluorescence, Staining