Anti sars cov 2 spike mouse mab 1a9

Maternal blood and cord blood were diluted in RNAlater in 1:1.3 ratio, placenta was preserved in RNAlater. Protein lysates were obtained from samples using RIPA buffer (150 mM NaCl, 25 mM Tris-HCl (pH 7.4), 1% NP-40, 0.5% sodium deoxycholate, 0.1% sodium dodecyl sulfate) containing Halt™ protease inhibitor cocktail (ThermoScientific). Cell Lysates were resolved by SDS/PAGE on a Bis-Tris methane 4–12% polyacrylamide gel and transferred to a nitrocellulose membrane, blocked with 5% skimmed milk diluted in PBS, an incubated overnight at 4 °C with anti-SARS-CoV-2 Spike mouse mAb (1A9, GeneTex) or anti-GAPDH rabbit polyclonal antibody (GTX100118, GeneTex), respectively, diluted 1:1000 or 1:5000 in blocking buffer. The membrane was washed in PBS buffer containing Tween-20 (0.1%) and then incubated for 1 h with horseradish peroxidase-conjugated anti-mouse and anti-rabbit secondary antibody (Jackson ImmunoResearch) diluted, respectively, 1:5000 and 1:10,000. The membrane was thoroughly washed, and proteins visualized using Immobilon Forte Western HRP substrate (Millipore). Samples were compared to a positive control of 293T cells constitutively expressing wild-type SARS-CoV-2 Spike protein. Dynamic range of the standard curve of the Spike protein western blot was 5 ng to 200 ng (Supplementary Fig. 2).

Maternal blood and cord blood were diluted in RNAlater in 1:1.3 ratio, placenta was preserved in RNAlater. Protein lysates were obtained from samples using RIPA buffer (150 mM NaCl, 25 mM Tris-HCl (pH 7.4), 1% NP-40, 0.5% sodium deoxycholate, 0.1% sodium dodecyl sulfate) containing Halt™ protease inhibitor cocktail (ThermoScientific).Cell Lysates were resolved by SDS/PAGE on a Bis-Tris methane 4–12% polyacrylamide gel and transferred to a nitrocellulose membrane, blocked with 5% skimmed milk diluted in PBS, an incubated overnight at 4°C with anti-SARS-CoV-2 Spike mouse mAb (1A9, GeneTex) or anti-GAPDH rabbit polyclonal antibody (GTX100118, GeneTex) respectively diluted 1:1,000 or 1:5,000 in blocking buffer. The membrane was washed in PBS buffer containing Tween-20 (0.1%) and then incubated for 1 h with horseradish peroxidase-conjugated anti-mouse and anti-rabbit secondary antibody (Jackson ImmunoResearch) diluted respectively 1:5,000 and 1:10,000. The membrane was thoroughly washed, and proteins visualized using Immobilon Forte Western HRP substrate (Millipore).