Black Book
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Brains are created in a lab from the foreskin of circumcised babies, and are then taught to play the game pong by a punishment and reward system in which the brain is sent electrical stimulation - failing to hit the ball overwhelms the brain with randomized signals, and hitting the ball sends it predictable, synchronized signals which are apparently pleasurable.
The foreskins are infected with a virus which transforms them into stem cells.
Video talking about all of this in depth: https://www.youtube.com/watch?v=67r7fDRBlNc
According to the video, baby foreskins are sold on the internet for about $480... What a great price to pay parents to circumcise their child and remove its most sensitive part of their genitalia in the process, leaving scars all over, and then sell it online to a lab, to be turned into a brain through infecting the foreskin with a virus and then torturing it to play pong all day. Sounds like a kike's wild daydream.
The medical research: https://www.cell.com/neuron/fulltext/S0896-6273(22)00806-6
The foreskins are infected with a virus which transforms them into stem cells.
Video talking about all of this in depth: https://www.youtube.com/watch?v=67r7fDRBlNc
According to the video, baby foreskins are sold on the internet for about $480... What a great price to pay parents to circumcise their child and remove its most sensitive part of their genitalia in the process, leaving scars all over, and then sell it online to a lab, to be turned into a brain through infecting the foreskin with a virus and then torturing it to play pong all day. Sounds like a kike's wild daydream.
The medical research: https://www.cell.com/neuron/fulltext/S0896-6273(22)00806-6
Initial work was conducted using a control hiPSC line supplied by the Gene Editing Facility at the Murdoch Children’s Research Institute (ATCC® PCS-201-010) from an ATCC PCS-201-010 background and transferred under a Material Transfer Agreement. ATCC line has been validated as per https://www.atcc.org/products/pcs-201-010 and comes from an XY donor isolated from neonatal foreskin. Later work involved an hiPSC lines used in this work constitutively expressing fluorescent reporters under control of the glyceraldehyde 3-phosphate dehydrogenase (GAPDH) promoter (cell lines were generated by Professor Edouard G. Stanley and colleagues from the Murdoch Children’s Research Institute and provided under a Material Transfer Agreement) (Kao et al., 2016
). The GAPDH gene encodes a protein critical in the glycolytic pathway, whereby ATP is synthesised from glucose. As this function is highly conserved across multiple cell types GAPDH is ubiquitously expressed at high levels across multiple cell types, making it a suitable gene for which to base a gene-expression system (Barber et al., 2005
). RM3.5 line validation is reported in (Barber et al., 2005
) and comes from an XY donor isolated from neonatal foreskin. This transgene expression system, termed GAPTrap, involves the insertion of the specific reporter gene into the GAPDH locus in hiPSCs using gene-editing technology (Kao et al., 2016
). For this study, RM3.5 GT-GFP-01 constitutively expressing green fluorescent protein under the GAPDH promoter was utilised. The RM3.5 hiPSC line was initially derived from human foreskin fibroblasts and reprogrammed using the hSTEMCCAloxP four factor lentiviral vector as reported previously (Somers et al., 2010
). All procedures described below were applied to be both cell lines. Both lines were maintained in an undifferentiated, pluripotent state in a feeder-free system using E8 media (Thermo Fisher Scientific, Carlsbad, USA) supplemented by a Penicillin/streptomycin solution at 5 μL/mL. Cells were plated on T25 353108 Blue Vented Falcon Flasks (Corning, Durham, USA) that were coated approximately 1 h prior with extracellular matrix vitronectin (Thermo Fisher Scientific, Carlsbad, USA).