This is shocking. I won't post a link, but you will know where to find it.
ERV has switched the labels from one western blot in Lombard et al. that was looking for the presence of ENV protein and ascribed them to the western blot data presented by Mikovits in Canada, when that western blot was constructed to detect the presence of GAG protein. The control lane in the western blot data was for gag protein and not env protein as claimed by ERV.
Here is Mikovits slide from Canada. As you can see it is a WB using goat antibody to gag. Lane 8 cannot refer to SFFV env because she is testing for gag.
I will post the 2 Western Blots from Lombardi et al. at the bottom of the screen. This is the description in Lombardi that goes with them.
(C) Lysates of activated PBMCs from healthy donors (lanes 1, 2, 4, 5, and 7) or
from CFS patients (lanes 3 and 6) were analyzed by Western blots using rat
mAb to SFFV Env (top panel) or goat antiserum to MLV p30 Gag (bottom
panel). Lane 8, SFFV-infected HCD-57 cells. Molecular weight (MW) markers
in kilodaltons are at left.
As you can see the top
one that ERV uses the labels from is western blots using rat
mAb to SFFV Env (top panel)
As you can see the bottom one
that ERV then takes the gel from is the western blot using goat
antiserum to MLV p30 Gag
So ERV would you like to explain why you don't know your env from you gag?
ERVs new creation is below the Lombardi et al. western blots.