146 cell culture 147 immortalized mouse renal tubular epithelial cells rtecs Search Results


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ATCC 146 cell culture 147 immortalized mouse renal tubular epithelial cells rtecs
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ATCC tubular epithelial cells rtecs
Tubular Epithelial Cells Rtecs, supplied by ATCC, 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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ATCC rat renal tubule epithelial cells
Trps1 promotes the proliferation of renal tubular <t>epithelial</t> cells after H/R. Renal tubular epithelial cells <t>(NRK-52E)</t> were subjected to hypoxic conditions for 4 hours followed by reoxygenation (H/R model). (A) After H/R, the PCNA and trps1 levels of NRK-52E cells were detected by Western blotting, and (B and C) the relative levels to β-actin were quantified (*P<0.05 versus control). (D) The immunohistochemical analyses for Trps1 and PCNA coexpression in NRK-52E cells were performed at 6 and 24 hours after H/R injury. (E) The PCNA protein levels were increased in Trps1-overexpressed NRK-52E cells at 24 hours after H/R, and (F) its relative levels to β-actin were quantified. (G) The PCNA protein levels were reduced in Trps1 knockdown NRK-52E cells at 24 hours after H/R, and (H) its relative levels to β-actin were quantified (*P<0.05 versus 0h).
Rat Renal Tubule Epithelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC human renal tubular epithelial cells rtecs hk 2
Trps1 promotes the proliferation of renal tubular <t>epithelial</t> cells after H/R. Renal tubular epithelial cells <t>(NRK-52E)</t> were subjected to hypoxic conditions for 4 hours followed by reoxygenation (H/R model). (A) After H/R, the PCNA and trps1 levels of NRK-52E cells were detected by Western blotting, and (B and C) the relative levels to β-actin were quantified (*P<0.05 versus control). (D) The immunohistochemical analyses for Trps1 and PCNA coexpression in NRK-52E cells were performed at 6 and 24 hours after H/R injury. (E) The PCNA protein levels were increased in Trps1-overexpressed NRK-52E cells at 24 hours after H/R, and (F) its relative levels to β-actin were quantified. (G) The PCNA protein levels were reduced in Trps1 knockdown NRK-52E cells at 24 hours after H/R, and (H) its relative levels to β-actin were quantified (*P<0.05 versus 0h).
Human Renal Tubular Epithelial Cells Rtecs Hk 2, supplied by ATCC, 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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ATCC mouse renal tubule epithelial cells mtecs
Trps1 promotes the proliferation of renal tubular <t>epithelial</t> cells after H/R. Renal tubular epithelial cells <t>(NRK-52E)</t> were subjected to hypoxic conditions for 4 hours followed by reoxygenation (H/R model). (A) After H/R, the PCNA and trps1 levels of NRK-52E cells were detected by Western blotting, and (B and C) the relative levels to β-actin were quantified (*P<0.05 versus control). (D) The immunohistochemical analyses for Trps1 and PCNA coexpression in NRK-52E cells were performed at 6 and 24 hours after H/R injury. (E) The PCNA protein levels were increased in Trps1-overexpressed NRK-52E cells at 24 hours after H/R, and (F) its relative levels to β-actin were quantified. (G) The PCNA protein levels were reduced in Trps1 knockdown NRK-52E cells at 24 hours after H/R, and (H) its relative levels to β-actin were quantified (*P<0.05 versus 0h).
Mouse Renal Tubule Epithelial Cells Mtecs, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/146+cell+culture+147+immortalized+mouse+renal+tubular+epithelial+cells+rtecs/TCMK-1/pm37248964-51-11-24
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mouse renal tubule epithelial cells mtecs - by Bioz Stars, 2026-09
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Image Search Results


Trps1 promotes the proliferation of renal tubular epithelial cells after H/R. Renal tubular epithelial cells (NRK-52E) were subjected to hypoxic conditions for 4 hours followed by reoxygenation (H/R model). (A) After H/R, the PCNA and trps1 levels of NRK-52E cells were detected by Western blotting, and (B and C) the relative levels to β-actin were quantified (*P<0.05 versus control). (D) The immunohistochemical analyses for Trps1 and PCNA coexpression in NRK-52E cells were performed at 6 and 24 hours after H/R injury. (E) The PCNA protein levels were increased in Trps1-overexpressed NRK-52E cells at 24 hours after H/R, and (F) its relative levels to β-actin were quantified. (G) The PCNA protein levels were reduced in Trps1 knockdown NRK-52E cells at 24 hours after H/R, and (H) its relative levels to β-actin were quantified (*P<0.05 versus 0h).

Journal: Journal of the American Society of Nephrology : JASN

Article Title: Transcription Factor Trps1 Promotes Tubular Cell Proliferation after Ischemia-Reperfusion Injury through cAMP–Specific 3′,5′-Cyclic Phosphodiesterase 4D and AKT

doi: 10.1681/ASN.2016010009

Figure Lengend Snippet: Trps1 promotes the proliferation of renal tubular epithelial cells after H/R. Renal tubular epithelial cells (NRK-52E) were subjected to hypoxic conditions for 4 hours followed by reoxygenation (H/R model). (A) After H/R, the PCNA and trps1 levels of NRK-52E cells were detected by Western blotting, and (B and C) the relative levels to β-actin were quantified (*P<0.05 versus control). (D) The immunohistochemical analyses for Trps1 and PCNA coexpression in NRK-52E cells were performed at 6 and 24 hours after H/R injury. (E) The PCNA protein levels were increased in Trps1-overexpressed NRK-52E cells at 24 hours after H/R, and (F) its relative levels to β-actin were quantified. (G) The PCNA protein levels were reduced in Trps1 knockdown NRK-52E cells at 24 hours after H/R, and (H) its relative levels to β-actin were quantified (*P<0.05 versus 0h).

Article Snippet: Reagents Rat renal tubule epithelial cells (NRK-52E) were purchased from the American Type Culture Collection (Manassas, VA).

Techniques: Western Blot, Control, Immunohistochemical staining, Knockdown