bs-8688R Search Results


anti pod1 tcf21  (Bioss)
93
Bioss anti pod1 tcf21
The expression of gene and protein levels of Aqp1 (Aquaporin water channel 1) and <t>Tcf21</t> <t>(Pod1)</t> were examined in PND6 rat kidneys kept at 4°C for 48h (A, B, E-G) or 72h (C, D) in the presence of medium (Control/0) or 1000 μg/mL DAFP1 or TmAFP, in comparison to kidneys frozen at the time of dissection (Time zero; T0). The kidneys of 3 rats were used per condition for 48h cold exposure and 2 to 3 rats per condition for 72h cold exposure. After 48h cold treatment, for each rat, one kidney was frozen for mRNA analysis and the other kidney was fixed in paraformaldehyde for immunofluorescence analysis. After 72h cold treatment, all kidneys were processed for qPCR analysis. The mRNA levels of Tcf21 (A, C) and Aqp1 (B, D) were determined by qPCR analysis and normalized to GAPDH. Gene expression in control and DAFP1- or TmAFP- treated tissues kept in cold condition is expressed as fold change of the levels measured in samples frozen after dissection (T0). Statistical significance: * p≤0.05, ** p≤0.01. (E-G) Representative pictures showing the general morphology and immunofluorescence signals of Tcf21 and Aqp1 in kidneys at time zero (E) vs tissues kept at 4°C for 48h with medium (Control) (F) or 1000 μg/mL DAFP1 (G). White arrows point at glomeruli, red arrows point at tubules, and red stars indicate areas of tissue degeneration.
Anti Pod1 Tcf21, 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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Average 93 stars, based on 1 article reviews
anti pod1 tcf21 - by Bioz Stars, 2026-02
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The expression of gene and protein levels of Aqp1 (Aquaporin water channel 1) and Tcf21 (Pod1) were examined in PND6 rat kidneys kept at 4°C for 48h (A, B, E-G) or 72h (C, D) in the presence of medium (Control/0) or 1000 μg/mL DAFP1 or TmAFP, in comparison to kidneys frozen at the time of dissection (Time zero; T0). The kidneys of 3 rats were used per condition for 48h cold exposure and 2 to 3 rats per condition for 72h cold exposure. After 48h cold treatment, for each rat, one kidney was frozen for mRNA analysis and the other kidney was fixed in paraformaldehyde for immunofluorescence analysis. After 72h cold treatment, all kidneys were processed for qPCR analysis. The mRNA levels of Tcf21 (A, C) and Aqp1 (B, D) were determined by qPCR analysis and normalized to GAPDH. Gene expression in control and DAFP1- or TmAFP- treated tissues kept in cold condition is expressed as fold change of the levels measured in samples frozen after dissection (T0). Statistical significance: * p≤0.05, ** p≤0.01. (E-G) Representative pictures showing the general morphology and immunofluorescence signals of Tcf21 and Aqp1 in kidneys at time zero (E) vs tissues kept at 4°C for 48h with medium (Control) (F) or 1000 μg/mL DAFP1 (G). White arrows point at glomeruli, red arrows point at tubules, and red stars indicate areas of tissue degeneration.

Journal: Toxicology letters

Article Title: Toxicity profiles and protective effects of antifreeze proteins from insect in mammalian models

doi: 10.1016/j.toxlet.2022.07.009

Figure Lengend Snippet: The expression of gene and protein levels of Aqp1 (Aquaporin water channel 1) and Tcf21 (Pod1) were examined in PND6 rat kidneys kept at 4°C for 48h (A, B, E-G) or 72h (C, D) in the presence of medium (Control/0) or 1000 μg/mL DAFP1 or TmAFP, in comparison to kidneys frozen at the time of dissection (Time zero; T0). The kidneys of 3 rats were used per condition for 48h cold exposure and 2 to 3 rats per condition for 72h cold exposure. After 48h cold treatment, for each rat, one kidney was frozen for mRNA analysis and the other kidney was fixed in paraformaldehyde for immunofluorescence analysis. After 72h cold treatment, all kidneys were processed for qPCR analysis. The mRNA levels of Tcf21 (A, C) and Aqp1 (B, D) were determined by qPCR analysis and normalized to GAPDH. Gene expression in control and DAFP1- or TmAFP- treated tissues kept in cold condition is expressed as fold change of the levels measured in samples frozen after dissection (T0). Statistical significance: * p≤0.05, ** p≤0.01. (E-G) Representative pictures showing the general morphology and immunofluorescence signals of Tcf21 and Aqp1 in kidneys at time zero (E) vs tissues kept at 4°C for 48h with medium (Control) (F) or 1000 μg/mL DAFP1 (G). White arrows point at glomeruli, red arrows point at tubules, and red stars indicate areas of tissue degeneration.

Article Snippet: The sections were then incubated with anti-Aquaporin 1 (AQP1) antibody (ab189291, Abcam, Cambridge, UK) or anti-POD1 (Tcf21) (bs-8688r, Bioss Antibodies, Woburn, MA) antibody diluted in PBS containing 10% BSA, 0.1% Triton-X 100, and donkey serum overnight at 4°C.

Techniques: Expressing, Control, Comparison, Dissection, Immunofluorescence

List of qPCR primers

Journal: Toxicology letters

Article Title: Toxicity profiles and protective effects of antifreeze proteins from insect in mammalian models

doi: 10.1016/j.toxlet.2022.07.009

Figure Lengend Snippet: List of qPCR primers

Article Snippet: The sections were then incubated with anti-Aquaporin 1 (AQP1) antibody (ab189291, Abcam, Cambridge, UK) or anti-POD1 (Tcf21) (bs-8688r, Bioss Antibodies, Woburn, MA) antibody diluted in PBS containing 10% BSA, 0.1% Triton-X 100, and donkey serum overnight at 4°C.

Techniques: