I have run these westerns a billion times and something or the other doesn’t work out. For eg, my gel ran straight and fine but when I transfer the gel to my membrane, half of the membrane shows no protein and the other half shows this weird curvy transfer. For context, I ran precast gel 4-12% transferred to membrane using iBLOT P0 dry transfer. Then, I cut the membrane into half (the two halves being biological replicates). One half shows barely anything and the other membrane is curved. What am I doing wrong? Samples are lyses in SDS licor loading buffer