WebWestern blot analysis of extracts from COS cells, untreated or TPA-treated, using Bad Antibody #9292 (right) or Phospho-Bad (Ser112) Antibody (left). Western blot analysis of Bad fusion protein phosphorylated by CKII or PKA in vitro, using Phospho-Bad (Ser112) Antibody (upper) or Bad Antibody #9292 (lower). 1/3 Image Gallery WebWestern blot analysis of extracts from 293 or SK-N-MC cells treated with UV (40 mJ/cm2), using Phospho-SAPK/JNK (Thr183/Tyr185) Antibody (upper) or SAPK/JNK Antibody (lower). Simple Western™ analysis of lysates (0.1 mg/mL) from 293 cells treated with UV (50mJ, 0.5 hour recovery) using Phospho-SAPK/JNK (Thr183/Tyr185) Antibody #9251.
Protocols - Western - PhosphoSolutions
WebWe further show that PEDV infection and its N protein overexpression, although they upregulated STAT1 transcription level, could significantly block poly(I·C) and IFN-λ3-induced STAT1 phosphorylation and nuclear localization. Western blotting revealed that PEDV and its N protein promote STAT1 acetylation via downregulation of HDAC1. WebApr 7, 2024 · m Western blot analysis shows that overexpression of SARS-CoV-2 N protein induces and promotes Smad3 phosphorylation and nuclear translocation in HK-2 cells under high AGE conditions (50 μg/ml ... ray cole hanging with winners
Tips for Detecting Phosphoproteins by Western Blot
Web1 day ago · Regardless of their specificity, with one exception, the phospho-Tau antibodies tested were found to not detect the unphosphorylated protein. Conclusions: We identify Tau antibodies across all categories (total, PTM-dependent and isoform-specific) that can be employed in Western blot and/or immunohistochemistry applications to reliably detect ... WebProtein Membrane Blot: -PVDF membrane is recommended. -Refer to Western Blot Protocol (up to Protein Transfer) to prepare protein membrane blot. Lambda Phosphatase Enzyme: Sigma Aldrich product, includes 10X phosphatase buffer … WebPhospho-EGFR (Tyr1068) Antibody (44-788G) in ICC/IF Immunofluorescence analysis of Phospho-EGFR (Tyr1068) was performed using 70% confluent log phase A-431 cells treated with 200 ng/mL of EGF for 10 minutes. ray cole bio