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Post by bannanny on Sept 19, 2010 13:34:44 GMT -5
I think you're right ruth... and I LOOOOOOVE your "electrospinning" thread too. Everything I've read so far of what you're posting seems to define exactly what I "see" goin on all around me in the environment and what I've been trying to explain for such a long time now.
Don't know what to do or say about it all yet... but with Berkeley now finding a way to make it controllable gives me hope!
love ya ~~ bannanny
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Post by cyn on Sept 20, 2010 5:02:54 GMT -5
Hey Ruth,
I am sure you are right about all this, but I'm unable to process this as it applies to us.
Sounds like they knew humans would be affected by the QD's back in 2004, yet they went ahead or gave their information to Ventner and the likes to aide them in project Morgellons.
Ruth, the only blue I see has always represented deep pools of gel. Regular gel appeared as silverish until it got deeper and turned blue. There have been blue circle dots of course lined up with the rest of course. This occurs during the process of building a fiber, like what the gel does when left on a slide.
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Post by toni on Sept 20, 2010 9:08:48 GMT -5
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Post by bannanny on Sept 20, 2010 13:43:03 GMT -5
I've been seeing blue sparks and blue hues of light in the air around me for quite some time now... seen alot of silver fluid looking stuff too cyn, so I know there's definitely SOMETHING blue and silvery in morgellons. I think it was about a year ago that I started trying to contact physicists about our mess ruth. I sent pics and explanations... but of course never ever got a reply. I saved a list of noteable ones tho, some of whom I wrote to. If anyone else wants to have a go at them, here's the link for ya... en.wikipedia.org/wiki/List_of_physicistsI sure do like what you're finding ruth... I definitely feel it has a whole lot to do with what's happening to us and around us. If I only knew where to take it from here. I'm so very tired (I know we all are) of trying to get attention from those who could help us but don't even seem to wanna get their hands in it at all. I know if I were a researcher and had any kind of degree I sure would be interested in wanting to solve this puzzle. Isn't that what scientists are supposed to be made of... to have the curiuosity to solve something no one else has yet been able to solve? Seems not these days huh? Seems not when it comes to morgellons anyway. big hugs ~~ bannanny
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Post by skytroll on Sept 20, 2010 21:30:25 GMT -5
You got them on the run and the buckyball oocytes are involved in the polarity.
Beginning process was the bacteriophage, the injectisome is made from yersinia pestis.
The initiation, then the other cells form, but the quantum directs its movement and charge.
Execellent observations my friend, and super finds.
Keep at it ruth, full speed around the bend!
Skytroll
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Post by skytroll on Sept 20, 2010 21:57:15 GMT -5
CdSe can cause pellagra(excessive selenium ) this is terrible, had a dose of it myself. Selenium cadium selenium: Ruth! We have it narrowed down, or You do! These are PHOTONS...not electrons, not neutrons, not protons, but PHOTONS, are based on light............................... But the core is this: =========================== (CdSe)ZnS Core−Shell Quantum Dots: Synthesis and Characterization of a Size Series of Highly Luminescent Nanocrystallites Bet they are hex form? ========================== We report a synthesis of highly luminescent (CdSe)ZnS composite quantum dots with CdSe cores ranging in diameter from 23 to 55 Å. The narrow photoluminescence (fwhm ≤ 40 nm) from these composite dots spans most of the visible spectrum from blue through red with quantum yields of 30−50% at room temperature. We characterize these materials using a range of optical and structural techniques. Optical absorption and photoluminescence spectroscopies probe the effect of ZnS passivation on the electronic structure of the dots. We use a combination of wavelength dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, small and wide angle X-ray scattering, and transmission electron microscopy to analyze the composite dots and determine their chemical composition, average size, size distribution, shape, and internal structure. Using a simple effective mass theory, we model the energy shift for the first excited state for (CdSe)ZnS and (CdSe)CdS dots with varying shell thickness. Finally, we characterize the growth of ZnS on CdSe cores as locally epitaxial and determine how the structure of the ZnS shell influences the photoluminescence properties. pubs.acs.org/doi/abs/10.1021/jp971091y====================== what is the ZnS grown on CdSe cores? Note the photoluminescence! bioilluminent! ======================= Coming UNGLUED, others are looking! ================= CdSe quantum dots induce superoxide stress in engineered biosensor bacteria That biosensor bacteria, is the the DICTY, listed above in inventions......... A panel of genetically-engineered Escherichia coli biosensor bacteria, responsive to chemical stressors inducing heat shock, DNA damage, oxidative stress (peroxide- and superoxide-type) and fatty acid metabolism interference, was used to characterize the chemical effect of CdSe quantum dot exposure. Results implicate a primary mode of superoxide-type stress toxicity that is dependent upon quantum dot dose, size, and chain length of capping agent, and are consistent with results from other reports employing mammalian cell lines. Imaging studies confirm association of quantum dots with lipophilic regions of the biosensor bacteria (i.e., inner/outer membranes, cell wall, periplasmic space), and demonstrate intracellular alteration of the quantum dot lattice. Corroboratory experiments with superoxide stress mutants and antioxidant amendments confirm oxidative stress while also implicating destabilization of quantum dots. Keywords Biosensor, superoxide stress, quantum dot, CdSe, nanotoxicity informahealthcare.com/doi/abs/10.1080/17435390802546089?journalCode=nan===================================== Well Citizen Physicists on the prowl. Since they are so greedy with their pure science, we have to do this ourselves. We are showing them, by our observations. I study the photos folks, and some really strange things are seen, so different yet alike in the sense that stem cells and progenitor cells were used as are the newer quantum dots and sensors, which can turn into stem cells replications or formations. Like this one and this is a big one, the sensors, are made from Dicty thanks to others searching in other directions....... ========================= Ni nanowire that has been grown into direct contact with one of the Dictyostelium cells of FIG. 2 after NiSO4 was added to the buffer. www.faqs.org/patents/app/20090200170Read more: www.faqs.org/patents/app/20090200170#ixzz107yvucU5www.freepatentsonline.com/EP1005568.pdf=================== toni, your questioning the little ball in ruths video, got me to thinkin......and you are so right it has a purpose. You all are great, and you know what, it is a process, all of us have observed and felt the process in our bodies at one point or another. that is why is different, because, it is not one entity, it is stem cells progenitors cells, inorganic substances as well, and the photons, as our "london" said quite a while ago! I remember Orions, gnat as well, it is of importance to some of us, because this is all around us in certain environments. And yes, there is a bug, there is fungi, conjugation, there is an injectisome, and an insectisome. stem cells and progenitor cells from insects, protozoans, archaea, under the sea protozoans, and rotifers and plants, ribozymes, roots of plants......mouse gene, fruit fly, worm, a. nidulans, s. cerevisciae, s pombe, we have found the injectisome, which is from yersinia pestis. Put the needle is what I am looking for now. Needle as in stinger apparatus....not just bee, although there is a "fairy wasp" or parasitoid wasp, as london had mentioned as well. But, the progenitor cell of the stinger and the stinger gene is all that was needed! and so on. But, Ruth, you have the controlling mover, the photon, which is a quantum dot. YaaaaaaaaaaaaaaHOOOOOOOOOOOOOOOOOOOOOO! skytroll
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Post by skytroll on Sept 20, 2010 22:02:06 GMT -5
Ruth,
It is time release agent though, so we need the bio, the chem, the inorganics, the physicists.
the quantum is the end stage. is the controller, but the stem cells are already in us.
Scary crap.
But, if the process can be stopped, we will need the molecularists, the microbiologists, the geologists(minerals), the metalloprotein folks, geneticists to look for the stem cells and progenitors used.
Convergent specialists............Kurzweil knows all about them............as does Venter Hamilton Smith, Stephen Mann...... etc.......
Many High notch scientists are out there Way up there!
They may or may not help us.
But, we can only try, folks...............
There is the spark of life, from above, and the filament of life from below, all within the source of life itself!
Not the deception science, light from below and filament from above!
Skytroll
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Post by toni on Sept 21, 2010 8:13:32 GMT -5
Sky,
I find the Yersenia Pestis veeeery interesting, because "of all things" I was tested for that when I'd gone to the hosp a couple of years ago. See...when they said they were testing me for (that) I thought, WHY THAT of all things? Hummmm
Sky, I do think much of what you said too is involed. What do you think about the Magnetotactic bacteria in correlation with "the lunar cycle and Morgs cycle" seeming to have a possible parallel of sensations many of us feel. I believe cytokine storms (are seriously involved) but that's another conversation.
But the macro observations under the scope, just wondering your thoughts of the macro magentotactic?
Ruth keep up the great work, thank you.
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Post by skytroll on Sept 21, 2010 14:41:05 GMT -5
toni, You asked: Sky, I do think much of what you said too is involed. What do you think about the Magnetotactic bacteria in correlation with "the lunar cycle and Morgs cycle" seeming to have a possible parallel of sensations many of us feel. I believe cytokine storms (are seriously involved) but that's another conversation. I think the blue is from dinoflagellates, when shaken in a jar it creates a blue light, that is the bioilluminent element. The magnetic has to have an ferritin, or iron element to attract the magnetic particles, which are most likely in the quantum dot itself. However there is magnetic bacteria that has to be the signal. So the magnetic bacteria could be in the yersinia pestis bacteriophage injectisome, which set the stage for the quantum dot to recognize the manetic quality in the bacteria. It appears there is a signalling that has to happen, most likely through the magnetic bacteria. I will find the specific dinoflagellate that has the bioillum blue light, I think it may be connected to a mycelia element, this blue light can be seen in abysses under earth or ocean floor, but that with the dino is making a blue light, lights up our bodies at night. Many have alternaria, cladosporium, candida, and penicillium, not penicillin, is different. someone had pencillium olsonii? was that Ruth? look at the first picture then compare to this web page photo, they are blue! www.dehs.umn.edu/iaq_fib_fg_gloss_penicilliumsp.htmwww.schimmel-schimmelpilze.de/penicillium-olsonii.htmlsomething about the number of electrical frequency? If go over 528 (the electrical number freq of human) then it cannot penetrate the body. So, if the alveoli of this is the bud, or pellicle that is what was used to attract the quantum dot. Does that make sense? If that signal is there, then the cell of the organism(s) would proliferate, being then directed by the control of the quantum dot. It would proliferate or replicate once the progenitor cell, for say actin or fibrin, the filaments in us, is intitiated by the injectisome which injects whatever dna is in the head of the bacteriophage. The thing about bacteriophage, is it needs to mutate, the viral components, once they are in the body, they then work to eat the bacteria which was put in there, by a previous bacteriophage, namely the llambda. However, the bacteria has to be there for the quantum dot to change its course, or to effect it polarity. If the buckyball oocyte is on the cell, it is directed by the quantum dot. C60 was used in the bucky ball which is caged inside the clathrin coated cage. That cage breaks down and releases the bucky ball nanome to attach to the cell. DNA aptamer: magnetic pull of moon. Had a lot of movement this am, then blood like clump came out of lesions. Lesions look like trail, the M13 I bel is snow white and 7 dwarfs, which are related to mother bacteriophage, nurse cell and note this pic: ge is germarium GSC (germ stem cell) genesdev.cshlp.org/content/12/23/3715/F4.large.jpgskytroll
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Post by skytroll on Sept 21, 2010 15:15:21 GMT -5
Since the pellagra, or as derm doc called pseudovesicles, meaning false vesicles, however, something made it. From my elbow down my arm is this trail, that look similar to the above pic. So a GSC cell most like inserted from the mother ship: the M13 which is a mutating bacteriphage, also carries the nanowire which has dicty as shown in the patent I posted, as a biosensor. There is a trail of this........just like the nasty trail on our skin, tells the story. Alveoli from certain fungi was used. The seven dwarfs are the even bacteriophages, like T2, T4 etc. "The murky origin of Snow White and her T-even dwarfs." THE T-even bacteriophages—T2, T4, and T6— represent facile experimental systems that are both relatively complex and meticulously well defined. They played essential roles in the birth and early nurturing of the field of molecular genetics and could serve simi- larly as model organisms for ecology. Identification of the source habitat from which these phages were iso- lated would be satisfying from an ecological as well as historical perspective. Here I infer, mostly from pub- lished materials, the habitats from which these three phages were isolated, plus I delve into the history of their host, Escherichia coli B. what is e. coli B vs the K-12 series. seems was used from 1918 on? ?? yersinia pestis, way back then..................the bacteriophage injectisome............ www.ncbi.nlm.nih.gov/pmc/articles/PMC1461100/pdf/10835374.pdf================== black plague............................. there was a problem, seems from this report of the two e.coli? ==================== "Studier, who participated in the study, said that while analyzing the history of E. coli B, Brookhaven researchers uncovered a laboratory mishap from the 1960s that had obscured the identities of the two different B strains. When scientists from different labs shared samples, one seems to have been mislabeled, and the true identity of each strain became unknown. " ........ "After learning about the historical mix-up and utilizing gene sequencing technology, the team was able to identify the differences between the two B strains, as well as determine the different laboratory manipulations used on the original 1918 strain. According to Brookhaven, this analysis shed light on the changes the bacterial genome undergoes due to standard laboratory procedures, such as chemical exposure, irradiation, and DNA transfer between genomes. “It’s amazing how much valuable information can be revealed by looking in detail at genome sequences,” said Studier, in a Brookhaven press release. According to Studier, the history of the B strains is important to those who want to work with E. coli. “Detailed information about these two strains is useful for future laboratory studies but is also important for companies who are using proteins made from E. coli B strains for medical purposes,” said Studier. “They want to know as much as possible about the bacterial strain, including where it came from.” The researchers compared the K-12 genome to those of the B strains, which were sequenced at KRIBB and Genoscope. “Although the B and K-12 strains came into the laboratory half a world apart, their genome sequences show that they are closely related,” said Studier. All three strains—K-12 and both B strains—were found to contain about 4.6 million nucleotide base pairs. “One of the most striking observations in comparing the B and K-12 genomes is the seemingly non-random distribution of single base-pair differences between them,” Sergi Maslov, a physicist at Brookhaven, said in a press release. The team published its results online on October 17, in three papers in the Journal of Molecular Biology. The research was supported by the Korean Ministry of Education, Science and Technology; the Consortium National de Recherche en Génomique; the GTL Program of the Office of Biological and Environmental Sciences and the Division of Materials Science within the Department of Energy Office of Science; the National Science Foundation; and the Defense Advanced Research Projects Agency. " www.biotechniques.com/news/Genome-sequencing-helps-define-history-of-E.-coli-B-strains/biotechniques-179477.html====================== So, since the formation of e-coli B............... ================= The seven dwarfs, not all even phages, made up of the even phages though. www.mun.ca/biochem/courses/3107/Lectures/Topics/bacteriophage.html==================== Channels and transporters: www.ls.manchester.ac.uk/research/researchgroups/channelsandtransporters/skyship
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Post by skytroll on Sept 21, 2010 15:31:55 GMT -5
It seems when you are looking for something, all of a sudden, things begin to make sense. 1918......... remake of the plague virus, remember Bush made a point of reading the booK? So, by way of bacteriphage eating a planted bacteria, which signals the quantum dot for poloarization, related to moon cycles, as well. just thinking here toni, but, they have to have something to do with this. hunchback protein? and so on. the literature tells the story. bicoid and hunchback genes......... hunchback of Notre Dame? www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=dbio&part=A1971&rendertype=figure&id=A1972holy maloney................................. or Holy Baloney........................................ ========== Origins of anterior/posterior polarity. www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=dbio&part=A1971skytroll
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Post by skytroll on Sept 21, 2010 15:57:02 GMT -5
Replisome: takes us right back to the bacteriophages......used as mutative replicates over and over. Mu or M13..... the mother, snow white......... definition of replisomes: ..."The replisome is a complex molecular machine that carries out replication of DNA. It is made up of a number of subcomponents that each provide a specific function during the process of replication.".................... stem cells replicate, progenitor cells divide (reproduce for a time) so we know this has to be from a particular stem cell. germarium stem cell from fruit fly. is related to fermentation........ mycoplasma fermentens.................... a formin..............means forms cell................. a protein from fruit fly? ?? or the embryo itself? www.uniprot.org/uniprot/P48608tinyurl.com/2ff5l7tskytroll
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Post by skytroll on Sept 21, 2010 17:48:03 GMT -5
or protein from the water flea?
has the barbed ends.
diaphanous;
mites and fleas.............
but the water flea is new.
Lederberg knew about the water fleas.
the book Arrowsmith?
Bacteriophages typhinium..........water flea......................
I do not know if clues or not.
skytroll
skytroll
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Post by bannanny on Sept 22, 2010 13:28:06 GMT -5
I'm gonna go buy some magnets and put 'em on the bottoms of my feet and see if they pull this sh*t outta me... I think.
Can't talk anymore today... got a little intestinal problem to deal with but I'll be back tomorrow.
love ya's ~~ bannanny
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Post by skytroll on Sept 22, 2010 20:40:25 GMT -5
Magnesium Citrate works folks, if you can stand the lemony. Has mag in it. If can get in all one place and blast those bas. tinkies out. Been eating black licorice and marshmellows, ingred in Dr Clark's remedies. Why do you think when you have a colonoscopy done, they make you drink this magnesium citrate? Clears out the quantum dots so they do not interfere with the scope. Yeah, ruth, mmmmmmmmmmmmmm indeed......... Have found the original biocell........ We are in the third stage.......... Process of Selection, folks!A three-stage model to explain the role of the cytoskeleton during axonal guidance is presented. The third stage shows the role of microtubules in the formation of an axon tube in a selected site.tinyurl.com/2539xudRead more: www.faqs.org/abstracts/Biological-sciences/Making-the-connection-cytoskeletal-rearrangements-during-growth-cone-guidance.html#ixzz10JRf3JYOtrying to get this out there, so we can find the things that will save us. skytroll
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Post by skytroll on Sept 22, 2010 21:37:03 GMT -5
The third stage: pages 16 note the fibers flayed and then the closing in on third photo. Done by photosynthesis, quantum dot........ Growth cone is already there, dynein.............. from tetrahymena... and other proteins from the wild............. dynein was found in tetrahymena a century and a half ago. That would be right around the time of Erasmus Darwin. Focus was put on Charles when it should have been put on what Erasmus Darwin achieved. He knew about the muscle motor, effects all nerves, muscles, especially smooth muscle. Dynein Actin cytoskeleton rearrangement is ongoing. Darwin knew of Duchenne, and Giavani, and the electrical stimulation of muscles. Smooth muscles involvement: =================== Alpha smooth muscle actin distribution in cytoplasm and nuclear invaginations of connective tissue fibroblasts " Abstract Alpha smooth muscle actin (α-SMA) was recently shown to be present in mouse subcutaneous tissue fibroblasts in the absence of tissue injury. In this study, we used a combination of immunohistochemistry and correlative confocal scanning laser and electron microscopy to investigate the structural organization of α-SMA in relation to the nucleus. Furthermore, we explored colocalization analysis as a method for quantifying the amount of α-SMA in close approximation to the nucleic acid marker, 4′,6-diamidino-2-phenyl-indole, dihydrochloride. Our findings indicate the presence of α-SMA within nuclear invaginations in close proximity to the nuclear membrane, but not in the nucleoplasm. Although the function of these α-SMA-rich nuclear invaginations is at present unknown, the morphology of these structures suggests their possible involvement in cellular and nuclear mechanotransduction as well as nuclear transport. Keywords Subcutaneous connective tissue - Alpha smooth muscle actin - Fibroblast - Nucleus - Quantum dots" www.springerlink.com/content/w18836h13747t562/alpha smooth muscle actin: alpha means new novel organism substituting for our native. ======== . The presence of these cells during the early remodeling may further indicate that α-smooth muscle actin containing fibroblastic cells are involved in the earliest stages of fiber bundle formation. The role and function of this special cell type for the anterior cruciate ligament needs to be further clarified onlinelibrary.wiley.com/doi/10.1016/S0736-0266%2801%2900109-7/abstract=============== fibroblastic cells: www.molvis.org/molvis/v14/a127/yang-fig2.htmlSo, Morgellons is the transformation of this, however, if on the extra x we carry diseases, those have been activated. This is where trisomy comes in....... a third strand within existing double strand, however, it was taken one step further, a double strand within a double strand. that newest latest strand involves the artificial dna strand. Linked with the bio strand that was created back when, from tetrahymena thermophile, dynein, Poly ethanol from the arabidopsis plant. and more. I will get the exact ingredients of the 3rd stage restructuring. Skytroll
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Post by skytroll on Sept 22, 2010 22:11:03 GMT -5
they knew about these a while ago. www.cdc.gov/ncidod/eid/vol5no2/goosney.htmWere used to make sure cytoskeleton was restructured. the only solution after that, would be the integration of artificial cell less systems. Quantum dots do that. Just listening to egg issues ............ Salmonella................. Watch for the shigella again...............and the tainted e-coli, that is how the k-12 primers and pyrimidines got in us. but, final stage:............... ================ :"“Synthetic biology” is a concept that has developed together with, or slightly after, “systems biology”. But while systems biology aims at the full understanding of large systems by integrating more and more details into their models, synthetic biology phrases different questions, namely: what particular biological function could be obtained with a certain known subsystem of reduced complexity; can this function be manipulated or engineered in artificial environments or genetically modified organisms; and if so, how? The most prominent representation of synthetic biology has so far been microbial engineering by recombinant DNA technology, employing modular concepts known from information technology. However, there are an increasing number of biophysical groups who follow similar strategies of dissecting cellular processes and networks, trying to identify functional minimal modules that could then be combined in a bottom-up approach towards biology. These modules are so far not as particularly defined by their impact on DNA processing, but rather influenced by core fields of biophysics, such as cell mechanics and membrane dynamics. This review will give an overview of some classical and some quite new biophysical strategies for constructing minimal systems of certain cellular modules. We will show that with recent advances in understanding of cytoskeletal and membrane elements, the time might have come to experimentally challenge the concept of a minimal cell. Keywords In vitro reconstitution, molecular motors, model membranes, artificial cells, microdroplets, biological oscillations informahealthcare.com/doi/abs/10.1080/10409230903074549?journalCode=bmgquantum dots in microdroplets? All-Liquid Photonic Microcavity Stabilized by Quantum Dots We demonstrate two simple methods to fabricate QD-stabilized toluene microdroplets in water as whispering gallery mode microscale resonators in an all-liquid phase. The toluene microdroplets show size-dependently high Q-factors up to 5100 resulting from the stable QD-loaded microdroplets. The highly QD-stabilized toluene microdroplet resonators in the all-liquid phase would be promising for multiple all-liquid lasers. pubs.acs.org/doi/abs/10.1021/ja909483wtoulene is in aerosol opeations. Skytroll skytroll
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Post by skytroll on Sept 22, 2010 22:13:36 GMT -5
So, lasers would control the quantum dots, our very bodies, our very cells, from a computer.
London was right.
Skytroll
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Post by skytroll on Sept 22, 2010 23:08:56 GMT -5
Ruth, Here's one for ya. == quantum dot wireless mechanotransducers: I do not think it worked, they only tested frogs, and how many of them have died? ========================== First Quantum Dots Applied To Living Organism The collaborating team of physicists and molecular biologists, microinject (inject a large quantity) quantum dots to very early frog embryos. Though in their first experiments a single quantum dot was toxic to the embryo, they purified the quantum dots so that a quantity of 10^9, or a billion, quantum dots could be injected to a single cell. The differentiation processes of their rapidly dividing cells make embryos highly sensitive to physical and chemical changes in their environment. The Rockefeller scientists are pleased that such a large number of quantum dots has proven safe. "We have made the quantum dot compatible with life," says Brivanlou. "Each safe application in an organism requires experimentation. But we're optimistic that if they work in frog embryos, they will work in other in vivo contexts." www.sciencedaily.com/releases/2002/11/021127071742.htm.."Quantum dots are nano-sized crystals that exhibit all the colors of the rainbow due to their unique semiconductor qualities. These exquisitely small, human-made beacons have the power to shine their fluorescent light for months, even years. But in the near-decade since they were first readily produced, quantum dots have excluded themselves from the useful purview of biology. Now, for the first time, this flexible tool has been refined, and delivered to the hands of biologists. ".............. BEACONS? 1,000 points of light...................come on........................... Skytroll
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Post by skytroll on Sept 22, 2010 23:09:53 GMT -5
Or maybe it did work and is part of the New Program.
skytroll
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