Blood Serum, complex Hydrogel, and Scaffolding of tissue like material.

A possible cause for triggering of rapid clots via cell mimicry agents. Complex technologies combined in aid of what seems to be a trans-humanist agenda.

The above image shows serum from centrifuged blood that has been sitting at room temperature for approximately 12 days. A sample from the vacutainer containing mostly plasma and separated gels was prepared on an RO and detergent cleaned slide for viewing in Dark field. It cleans well for our needs.

The video above shows a 20x speed capture of blood serum revealing what we believe to be the laminating of pre-alligned cell structures and cross linked colloidal molecules. We think these processes match technologies where a mixture of Nanoparticles and other materials laminate the aligned constructive guiders that appear to be like the dream weaver patterns caused by colloidal molecules and other linked material that we have consistently found across endless samples so far. There are complex material forming secretions from the faint cells layed in the ordered and linked tracks after they are coated in the other laminating materials.

From our previous research Colloidal molecules can secrete a large range of programmed products including cells or reactive structures, they can each have very unique properties programmed in to them. We believe there is likely biological products involved here also and that this process seems to possibly be mimicking tissue formations among other integrations. The networks and structuring are extensive. The serum is extremely loaded with nanoparticles, colloidal materials, suspect crystal formations, polymer substrates containing various particles with other products, microfuidic pump systems (chemical/material factories), Constructor rings, fibers, and more.

Most of these visual products would appear in literature to be the result of hydrogels saturated in the blood.

The initial droplet of serum under the slide is densely populated by particles, some cell structures, with a few fibers and NP loaded substrates. Localized charge phenomenon can be observed in areas of the slide, likely related to same or similar methods that cause zeta potential manipulation in the injectables and other sources. The zeta charges in those products are used to manipulate rapid entry of material in to cell membranes and to manipulate flows. This is likely also a technique employed in part of the microfluidic systems we will see later or in the next post if there is not room in this one.

Using UV light at two different wavelengths at once allows us to see the serum contaminants materializing particles at the edge of the droplet. This is regularly seen in the other sources or products we have tested. These particles are often absorbed in to what we shall call a ring constructor or sphere for now since there are several written papers that show a candidate for this kind of activity and we cannot be sure which is correct yet.

A ring constructor and other types of ring or cell looking constructors will selectively absorb particles formed from or stored as cargo in hydrogels found in the serum just as it seems to in the injectables and other sources. Pay attention to the other kind of guidance constructor located in the center of the 3 armed and 2 armed structures, small ones appear as a sphere, larger ones seem to have a bright ring and look less like a polymer sphere for reasons that are not entirely clear yet, this could be due to the programmed individuality. Material will align strategically in to the linked and patterned colloidal molecule based template structures after we force the laminating process to trigger off. In this case many variables speed up or trigger this process while on the slide and it is likely slightly different or maybe even slower in other places of the body where it may be occurring.

After the serum has finished the reactions it is able too before drying we can see clearly dehydrated and cracked spheres that look like polymer encapsulations. The outer ring of the membrane presumably has taken iron rich hemoglobin and concentrated it in a very specific positioning. It is most common that a sphere will be involved in the relationship that produces the colorful blue fiber like veins that stand proud. We see this in blood where it rapidly tears in from the cover slip edges and seems to also contain same concentrations of embedded material. The fact these fibrous networks seem to rapidly tear out from a sphere location upon droplet drying indicates an unnatural process with clearly very unusual behavior.

See here where there is a sphere structure which once floated like polymer microshpere. Bright colours can be seen at the tear site and most notably fibrous polymer networks branch out giving the impression of dried blood cracking open to reveal empty voids. But these are not voids, they are rapidly forming polymers with an unknown and very well ordered or consistent internal arrangement it would seem.

Due to the unintended triggering of these scaffolding events on the slide it looks as if though there is material which did not find its placing or finished constructing. They may not have fit the criteria to form under these conditions or in this kind of environment possibly. I would imagine that the blood is carrying a range of hydrogel based material and that some of its varying products are inclined to unpack with there constructors in other body locations. Just thoughts at the moment.

The matrix of particles and other material surrounds the fiber like networks above. The raised terrain of these rapid forming structures is easily seen. A great density of glistening particles fill the inner tubule of the fibers which seem more frosted and much less opaque while focused out.

A complex arrangement of fast formed polymer structures which all formed uniquely to each other where visual properties were observed. The colour of the glassy polymers and many other details vary intriguingly. The visual layout is rather mind boggling when you see intensely glowing red sheets next to completely opaque or clear sheets layered on other strange geometric formations.

Above: UV exploitation of constructive templating structures outside of the blood droplet area. The initial drop extended past these structures but quickly shrunk to exclude them from the lamination process. By the time events peaked and the lamination process had been triggered the only material which could be constructed further was in the path of said materials involved in overlaying lamination process.

We find samples can and do often exhaust their ability to go through to the next morphological stages if the materials in the matrix are consumed or run out, not jut because of drying out, PH, etc. We see this for most aspects of this technology in multiple samples, they will only trigger and unfold correctly under specific condition. You may see it that outside of their intended environment they are extremely unstable and will behave very differently at many stages. The wrong conditions can show morphology or behavior that can often match what would seem like the flow of another product in literature. For example some hydrogels are meant to polymerize as part of the design requirement or maybe not meant to for another intended product design but will be seen doing so if the PH, light, Electrical, or other criteria goes out of range. When the one that is not supposed to polymerize does so and the polymerization is not beneficial to that particular design then that hydrogel is then seen as misbehaving. Other stages of the technology seem to be just as volatile, maybe not breaking the product but altering shape, form and appearance even if still achieving its intended developments.

I am sure others will jump to conclusions with this material based on visuals. We think we understand these structures and processes in more detail than is shown here but will observe things much more closely before referencing the wrong or right papers. There is similarity between many of the papers based on hydrogels showing these kinds of scaffolds and varying constructors.

Analysis using HPLC and Raman microscopy would help confirm these particular details. Without that kind of comparative analysis these are just the processes of anything or any paper that is remotely close by visual comparisons and by vague descriptions. The visuals and other criteria so far are absolutely indicative of what we think we can see when you put it all together, but is not enough to target that correct selection of design products specifically without more data to back it.

4x mag of serum droplet after reactions, assembly and drying out. Image on right is UV showing a few structres outside the droplet drying area which could not be laminated like the ones which fell inside.

These are brief and modular notes of what we have seen recently, it is only a small part of more complex processes and all the stages we have down so far need stitching together correctly so they form a correct product chain. For that reason it is best not to be too technical with these observations here.

The processes are so complicated that our walls are littered with long chains of stitched images which we adjust to place in closest order of morphology. Some seem right, some are unclear likely because of multiple pathways which have been observed and for which the behavior changes based on environmental factors that add complication where clarity is needed.

We need more answers asap!

We appreciate help towards the pricey lab gear for which we are not able to afford. Let us find definitive answers together.

Thank you all, much love as usual.

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ALSO a huge thank you to

koppykat

, YOU ARE AWESOME!