T1020 Search Results


99
New England Biolabs monarch dna gel extraction kit
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TargetMol dox
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FLIR Systems thermohygrometer camera t1020
Thermohygrometer Camera T1020, supplied by FLIR Systems, 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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Beijing Solarbio Science 1.0 m tris(hydroxymethyl)aminomethane (tris-hcl ) (ph 6.8) solarbio t1020
1.0 M Tris(Hydroxymethyl)Aminomethane (Tris Hcl ) (Ph 6.8) Solarbio T1020, supplied by Beijing Solarbio Science, 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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90
ATTO Corp e-pagel cat# e-t1020
E Pagel Cat# E T1020, supplied by ATTO Corp, 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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Bruker Corporation ir spectrophotometer bruker-alpha-t-1020
Ir Spectrophotometer Bruker Alpha T 1020, supplied by Bruker Corporation, 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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Danville Materials Inc flat number t1020
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Topscience Co Ltd adriamycin
Effects of luteolin (LUT) treatment on the viability and apoptosis of ADR-treated MPC-5 cells as well as the protein expressions of AKT1 and CASP3. (A) The viability of MPC-5 cells in the LUT (0, 100, 150, 200, 250 μM) groups was determined by cell counting kit-8 (CCK-8) assay. (B) CCK-8 assay was also performed again to detect the cell viability in the control, <t>adriamycin</t> (ADR), ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups. (C–D) The apoptosis rate of MPC-5 cells in the control, ADR, ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups was measured by flow cytometry. (E–F) The protein expressions of cleaved (Clea)-caspase-3, AKT1, and phosphorylated (p)-AKT1 were determined by Western blot, with GAPDH serving as the loading control.
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Genentech inc method of administration of ifg-1 t-1020/03
Effects of luteolin (LUT) treatment on the viability and apoptosis of ADR-treated MPC-5 cells as well as the protein expressions of AKT1 and CASP3. (A) The viability of MPC-5 cells in the LUT (0, 100, 150, 200, 250 μM) groups was determined by cell counting kit-8 (CCK-8) assay. (B) CCK-8 assay was also performed again to detect the cell viability in the control, <t>adriamycin</t> (ADR), ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups. (C–D) The apoptosis rate of MPC-5 cells in the control, ADR, ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups was measured by flow cytometry. (E–F) The protein expressions of cleaved (Clea)-caspase-3, AKT1, and phosphorylated (p)-AKT1 were determined by Western blot, with GAPDH serving as the loading control.
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Effects of luteolin (LUT) treatment on the viability and apoptosis of ADR-treated MPC-5 cells as well as the protein expressions of AKT1 and CASP3. (A) The viability of MPC-5 cells in the LUT (0, 100, 150, 200, 250 μM) groups was determined by cell counting kit-8 (CCK-8) assay. (B) CCK-8 assay was also performed again to detect the cell viability in the control, adriamycin (ADR), ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups. (C–D) The apoptosis rate of MPC-5 cells in the control, ADR, ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups was measured by flow cytometry. (E–F) The protein expressions of cleaved (Clea)-caspase-3, AKT1, and phosphorylated (p)-AKT1 were determined by Western blot, with GAPDH serving as the loading control.

Journal: Renal Failure

Article Title: Forecast and verification of the active compounds and latent targets of Guyuan decoction in treating frequently relapsing nephrotic syndrome based on network pharmacology

doi: 10.1080/0886022X.2023.2184654

Figure Lengend Snippet: Effects of luteolin (LUT) treatment on the viability and apoptosis of ADR-treated MPC-5 cells as well as the protein expressions of AKT1 and CASP3. (A) The viability of MPC-5 cells in the LUT (0, 100, 150, 200, 250 μM) groups was determined by cell counting kit-8 (CCK-8) assay. (B) CCK-8 assay was also performed again to detect the cell viability in the control, adriamycin (ADR), ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups. (C–D) The apoptosis rate of MPC-5 cells in the control, ADR, ADR + LUT-100, ADR + LUT-150, and ADR + LUT-200 groups was measured by flow cytometry. (E–F) The protein expressions of cleaved (Clea)-caspase-3, AKT1, and phosphorylated (p)-AKT1 were determined by Western blot, with GAPDH serving as the loading control.

Article Snippet: To mimic FRNS in vitro , MPC-5 cells were stimulated with 10 μM adriamycin (ADR, T1020, TopScience, China) for 6 h (h).

Techniques: Cell Counting, CCK-8 Assay, Control, Flow Cytometry, Western Blot