https://www.alecsatin.com/what-is-luciferase/
Green Fluorescent Protein – Cool Uses – HIV Virulence (conncoll.edu)
The avian retroviruses, (as referred to in the list of contents for the coronavirus BIOWEAPON): https://pubmed.ncbi.nlm.nih.gov/12584331/
HeLa cells as referenced in the ingredients list: https://www.hopkinsmedicine.org/henriettalacks/immortal-life-of-henrietta-lacks.html
Cervical cancer cells used in the CORONAVIRUS BIOWEAPON: https://www.hopkinsmedicine.org/henriettalacks/index.html
Intervirion Fusion. HIV-luc(ACE2) (500 ng of p24) was mixed with
1,000 ng of p24 of HIV-gfp particles incorporating ASLV-A
envelope, SARS-CoV S protein, or both envelopes in PBS at 4°C
for 30 min to allow binding. Samples were raised to 37°C for 15 min
to allow for conformational rearrangements. Virions were adjusted
to the desired pH with 0.1 M citric acid. PBS, TPCK-trypsin (final
concentration 10 gml), CTSL, cathepsin B (CTSB) (final concentrations 2 gml) or CTSL buffer alone was then added.
Recombinant CTSL (R & D Systems) was preactivated by incubation for 15 min at 10 gml in 50 mM Mes, pH 6.0, on ice.
Recombinant CTSB (R & D Systems) was preactivated in 25 mM
Mes, 5 mM DTT, pH 5.0, for 30 min at 25°C. After a 10-min
incubation at 25°C, proteolysis was halted by the addition of 300 l
of DMEM10 containing leupeptin (25 gml) and STI (75 gml).
Virions were then incubated at 37°C for 30 min to allow membrane
fusion. 100 l of the virion mixture was added in quadruplicate to
HeLa-Tva cells pretreated for 1 h with leupeptin (20 gml). The
cells were spin-infected and incubated at 37°C for 5 h. The medium
was replaced with fresh DMEM10 and the cells were assayed for
luciferase activity 40 h later.
‘GLOBALIST EXTERMINATION WINDOW TO WIPE-OUT HUMANITY IS RAPIDLY CLOSING – JOHN MOORE INTERVIEWED BY MIKE ADAMS’: Brighteon
‘COMMON PURPOSE EXPOSED’: https://www.cpexposed.com/
MASONIC SYMBOLISM IN YOUR FACE!!!!
