dynabeads protein a g (Santa Cruz Biotechnology)
Structured Review
Dynabeads Protein A G, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 4599 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dynabeads+protein+a+g/Stat3+Antibody/pm41834581-83-9-36
Average 96 stars, based on 4599 article reviews
Images
Related Articles
Incubation:Article Title: Oncogenic GPR161 Drives Melanoma Proliferation and Metabolic Activity through TXNIP Inhibition Article Snippet: Cells were lysed in ChIP lysis buffer on ice for 10 min, and chromatin was fragmented to ~250–750 bp by sonication (Sonics & Materials, Inc., USA). .. The diluted lysates were pre-cleared with 50 μl of Article Title: Oncogenic GPR161 Drives Melanoma Proliferation and Metabolic Activity through TXNIP Inhibition. Article Snippet: Cells were lysed in ChIP lysis buffer on ice for 10 min, and chromatin was fragmented to ~250– 750 bp by sonication (Sonics & Materials, Inc., USA). .. The diluted lysates were pre-cleared with 50 μl of Control:Article Title: Oncogenic GPR161 Drives Melanoma Proliferation and Metabolic Activity through TXNIP Inhibition Article Snippet: Cells were lysed in ChIP lysis buffer on ice for 10 min, and chromatin was fragmented to ~250–750 bp by sonication (Sonics & Materials, Inc., USA). .. The diluted lysates were pre-cleared with 50 μl of Article Title: Oncogenic GPR161 Drives Melanoma Proliferation and Metabolic Activity through TXNIP Inhibition. Article Snippet: Cells were lysed in ChIP lysis buffer on ice for 10 min, and chromatin was fragmented to ~250– 750 bp by sonication (Sonics & Materials, Inc., USA). .. The diluted lysates were pre-cleared with 50 μl of |
![( A ) Two paralogous ZAD-ZnF genes D19B and D19A are tandemly placed at the locus. ( B ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19A and D19B proteins. Two- to 4-hour embryos from corresponding homozygous strains were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( C ) Measurement of the embryo hatching rate. Embryos from corresponding homozygous full-locus deletion mutant adults were used for the analysis. ( D ) Confocal images of His2Av-emiRFP670 in embryos from WT or homozygous D19B[ Δ 1] mutant adults. The maximum-intensity–projected images of His2Av-emiRFP670 are shown. ( E ) Measurement of the embryo hatching rate. Maternal supply of D19B is essential for the correct progression of embryogenesis. ( F ) Schematic of the full-length D19B protein. ( G ) AlphaFold3 prediction of the D19B ZAD dimer. Protein structure was visualized using UCSF ChimeraX . ( H ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19B and WT/ΔZAD D19B rescue constructs reintroduced into the endogenous locus via recombinase-mediated cassette exchange (RMCE). Two- to 4-hour embryos from corresponding homozygous mutant adults were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( I ) Airyscan imaging of GFP-3xFLAG–tagged WT and ΔZAD D19B expressed from the endogenous locus. Images were taken ~15 min after entry into nc14. Embryos from corresponding homozygous strains were used for the analysis. The maximum-intensity–projected images are shown. ( J ) Measurement of embryo hatching rate. Embryos from corresponding homozygous RMCE strains were used for the analysis.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_7871/pmc12947871/pmc12947871__sciadv.ady7568-f5.jpg)