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Post by skyship on Mar 1, 2014 3:48:31 GMT -5
There are Janus (U of Pa)particles hydrophilic/hydrophobic and there is NH3 (U of Mi)Which, if either are correct, or is one fixing the other? Who in the h is the enemy here? Or is there something even more devious?
Why 2 kinds? Different strokes for different folks? Is there a war above us for our body carrier system? Bet there is~! I have seen black lines lain down above, and then white lines under them. So, what is going on, here? I guess some use the UN's planes and some use Evergreens? Depends on your poison? And who is controlling WHO? who works under UN. A bill is in Congress to get US out of UN. Or are Aliens involved in this? The GODS are coming back, because the gods of earth wish it so. ~!~!~! ---------------------------------- These are cryo-TEM and 3-D intensity profiles of (A and D) polygonal dendrimersomes. (B and E) Bicontinuous cubic particles co-exist with low concentration of spherical dendrimersomes. (C and F) These are micelles. (G and J) These are tubular dendrimersomes. (H and K) Rodlike, ribbon and helical micelles. (I and L) Disk-like micelles and toroids.www.azonano.com/images/news/NewsImage_17625.jpg***************************************************** *************************** BUT, U of MI is using NH3. For the Defense community~!oai.dtic.mil/oai/oai?verb=getRecord&metadataPrefix=html&identifier=ADA406313============================================== So if Ammonium at core or janus particle, we still are showing them coming out. So, they have sensors, biomonitors, etc. Can change genes, and do use the Laser, it seems.
This is without our consent~! They took our CO2....RuBisCo. All monsanto patents through U of Pa, Janus particle. well has different surfaces etc. kinda evasive on the definition.=================================================== soft-matter.seas.harvard.edu/index.php/Janus_Particles_Templated_from_Double_Emulsion_Droplets_Generated_Using_Microfluidics So, if they are in droplets we know from whence they come~!~!~!~! even nucleated snow, and those darn ole 'jumping genes" oops "jumping fleas" carrying the cold shock proteins and who knows what other janus particles and nucleated information.
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Post by skyship on Mar 1, 2014 13:20:47 GMT -5
These can be seen under regular microscope. So, why they fool us by using TEM and SEM is because they have to see inside them. so. it appears they are nano, same size as proteins in genes. Size of proteins, do we have a list for those? naw....... they are nano. are they really?
Remember RuBisCO molecules? which alter carbon dioxide, including humans. remember OMe?The OMe in ..some (pronounced sohm)? mersome......polymersome......dendrimersome........... S=wireless? ---------------------------- Rib o some:nicedefinition.com/Definition/Word/ribosome/ribosome.aspx-------------------------- Sohm?.....Ohm...........======================= =============== In the case of humans the N and the C terminals. Ohms in polymersomes?
Color changing molecular SENSORS:======================================= [[/b] Posted on 18. Aug, 2011 by Admin in technology It is helpful - even life-saving - to have a warning sign before a structural system fails, but, when the system is only a few nanometers in size, having a sign that’s easy to read is a challenge. A new report shows that a simple color change can signal such a warning. The authors started with the assumption that carefully assembled composites that respond intelligently to physical changes within a material could be useful as intrinsic sensors. They used near-infrared emissive supermolecular porphyrin-based fluorophore probes embedded within the hydrophobic core of a polymersome membrane. The researchers’ work involves two molecules: porphyrins, a class of naturally occurring pigments, and polymersomes, artificially engineered capsules that can carry a molecular payload in their hollow interiors.They hypothesized that polymersomes could be used as stress sensors if their membranes were embedded with a certain type of light-emitting porphyrins. The Penn researchers collaborated with the Therien lab at Duke, where the porphyrins were originally developed, to design polymersomes that were studded with the light-emitting molecules. When light is shined on these labeled polymersomes, the porphyrins absorb the light and then release it at a specific wavelength, or color. The Therien lab’s porphyrins play a critical role in using the polymersomes as stress sensors, because their configuration and concentration controls the release of light. “When you package these porphyrins in a confined environment, such as a polymersome membrane, you can modulate the light emission from the molecules,” Hammer said. “If you put a stress on the confined environment, you change the porphyrin’s configuration, and, because their optical release is tied to their configuration, you can use the optical release as a direct measure of the stress in the environment.” For example, the labeled polymersomes could be injected into the blood stream and serve as a proxy for neighboring red blood cells. As both the cells and polymersomes travel through an arterial blockage, for example, scientists would be able to better understand what happens to the blood cell membranes by making inferences from the stress label measurements. The researchers calibrated the polymersomes by subjecting them to several kinds of controlled stresses — tension and heat, among others — and measuring their color changes. The changes are gradations of the near infrared spectrum, so measurements must be made by computers, rather than the naked eye. Rapidly advancing body-scanning technology, which uses light rather than magnetism or radiation, is well suited to this approach. Other advances in medicine could benefit, as well. As cutting-edge pharmaceutical approaches already use similar molecular technology, the researchers’ porphyrin labeling system could be integrated into medicine-carrying polymersomes. The study was conducted by professor Daniel Hammer and graduate students Neha Kamat and Laurel Moses of the Department of Bioengineering in Penn’s School of Engineering and Applied Science. They collaborated with associate professor Ivan Dmochowski and graduate student Zhengzheng Liao of the Department of Chemistry in Penn’s School of Arts and Sciences, as well as professor Michael Therien and graduate student Jeff Rawson of Duke. “These kinds of tools could be used to monitor drug delivery, for example,” Kamat said. “If we have a way to see how stressed the container is over time, we know how much of the drug has come out.” And, though the researchers chose the engineered polymersomes due to the wide range of stress they can endure, the same stress-labeling technique could soon be applied directly to naturally occurring tissues. “One future application for this is to use dyes like these porphyrins but include them directly in a cellular membranes,” Kamat said. “No one has taken a look at the intrinsic stress inside a membrane so these molecules would be perfect for the job.” The work was supported by the National Institutes of Health, the National Science Foundation and its Materials Research Science and Engineering Center program and the National Center for Research Resources. Sensing membrane stress with near IR-emissive porphyrins. Neha P. Kamat, Zhengzheng Liao, Laurel E. Moses, Jeff Rawson, Michael J. Therien, Ivan J. Dmochowski, and Daniel A. Hammer PNAS 2011 ; published ahead of print August 15, 2011, doi:10.1073/pnas.1102125108 www.sciencedebate.com/science-blog/color-changing-molecular-stress-sensor[/quote]www.sciencedebate.com/sites/default/files/polymersome_porphyrin-release.pngEnhanced image of a polymersome changing color under stress. Image Credit: Upenn media service ========================================== proteins:Figure: Size-optimized phospholipid nanodiscs for structural studies of membrane proteins with NMR spectroscopy. Nanodiscs consist of lipids encircled by two copies of apolipoprotein A-1 (ApoA-1). The length of the ApoA-1 defines the diameter of the nanodisc. Truncated ApoA-1 constructs lead to smaller nanodiscs as monitored by negative-stain electron microscopy (EM), which are suitable for high-resolution structure determination by NMR spectroscopy. www.hfsp.org/sites/www.hfsp.org/files/Hagn2013a_0.gif
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Post by skyship on Mar 1, 2014 13:31:42 GMT -5
You will find the Janus particle patents, the Janus dendron, dendrimersome, the Monsanto patents through U of PA. Tons of them.
Google Ohms in Polymersomes.....
RuBisCO messes with the carbon in us, then the 3 amino added units, then the 3 functions: DNa methylation, histone modification and RNAi. Then the Janus particle or NH3 core (Tomalia brand), then micelles, dendrons, dendrites, dendrimersomes, dendrimers. etc. the ohm sensors, control by voltage, and magnetism.
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Post by skyship on Mar 1, 2014 13:34:08 GMT -5
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Post by skyship on Mar 5, 2014 18:50:08 GMT -5
Please See: Surface plasmon resonance thread. What we have to sort out are the TOOLS and the working or nonworking products.=========================== RIBOs? Smart material for your genome: looking for the architecture model~! ========================== SMART: Simple Modular Architecture Research Toolsmart.embl-heidelberg.de/smart/show_secondary.cgi?domain=RIBOc============================== First, Genome Editing: in form of ZINC FINGER> ===================
Reverse genetics in model organisms such as Drosophila melanogaster, Arabidopsis thaliana, zebrafish and rats, efficient genome engineering in human embryonic stem and induced pluripotent stem cells, targeted integration in crop plants, and HIV resistance in immune cells - this broad range of outcomes has resulted from the application of the same core technology: targeted genome cleavage by engineered, sequence-specific zinc finger nucleases followed by gene modification during subsequent repair. Such 'genome editing' is now established in human cells and a number of model organisms, thus opening the door to a range of new experimental and therapeutic possibilities.www.ncbi.nlm.nih.gov/pubmed/20717154?access_num=20717154&link_type=MED&dopt=Abstract[/quote]======================= So how was the "zinc finger" engineered and what is it made of?
One needs EDITING for the WRITTEN TEXT in the NATIVE GENOME~!======================== =============================== So, ZFNs nucleases and CoDa (context-dependent-assembly- A Platform for "genome wide alterations. again, what is the ZFN? ====================== Schematic overview of Context-Dependent Assembly (CoDA)Zinc fingers are represented as colored spheres (F1 = amino-terminal finger, F2 = middle finger, F3 = carboxy-terminal finger) and 3 bp DNA “subsites” are represented as colored rectangles. www.ncbi.nlm.nih.gov/pmc/articles/PMC3018472/figure/F1/
Were these used in the Schematic models or real time. real editing and clonging and alterations?
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Post by skyship on Mar 5, 2014 19:22:42 GMT -5
These are Artificial Restriction Enzymes: used in the ZFNs.
***************
===================================== So ZFNs are made with Restriction Enzymes Organic and Artificial: Directed evolution:
======================
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Post by skyship on Mar 5, 2014 19:51:27 GMT -5
ZFN suppliers: www.sigmaaldrich.com/life-science/zinc-finger-nuclease-technology.htmlNotice that RNAi or the RNAi www.sigmaaldrich.com/life-science/zinc-finger-nuclease-technology/learning-center/zfn-faqs.htmlSo, the molecular basis is not found...... hidden most likely. Three zinc fingers recognize nine base pairs, a sequence which would occur randomly several times in a large genome. However six fingers linked together would recognise a DNA sequence 18 basepairs in length, sufficiently long to constitute a rare address in the human genome. We have learned how to engineer longer runs of zinc fingers which can target longer DNA sequences. By adding functional groups to the engineered DNA binding domains, eg silencing or activation domains, novel transcription factors can be generated to up or downregulate expression of a target gene. Some recent applications by ourselves and others will be described: (i) the disruption of the infective cycle of infection by herpes simplex virus (ii) inhibition of HIV-1 expression (iii) activating the expression of erythropoietin (EPO) in a human kidney cell line (iv) activating the expression of vascular endothelial growth factor (VEGF) in a human cell line, and in an animal model. Postscript While it has long been known that TFIIIA binds RNA as well as DNA, there is now increasing evidence that zinc fingers are more widely used to recognize RNA. However the molecular basis of the recognition has remained elusive. We have recently determined the X-ray structure of a zinc finger RNA complex which reveals two modes of zinc finger binding, both different from that for DNA. www.med.miami.edu/mnbws/x49.xmlIs this what is used in the ncRNA? I bet it is. and later in the buckyball.
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Post by skyship on Mar 5, 2014 19:53:47 GMT -5
Interesting? Seeking to harness zinc finger potential, researchers and entrepreneurs collaborated to form Sangamo Biosciences in 1995, which emerged as the sole commercial provider of the protein. Today, the Sangamo monopoly raises a variety difficult ethical and economic questions about intellectual property within the zinc finger field, and synthetic biology as a whole. As an open-source alternative to Sangamo’s proprietary system and commercial dominance, Keith Joung and others have published the OPEN system[5] of zinc finger creation. However, while the OPEN system and subsequent improvements are promising for massive zinc finger production, the methods are difficult and time-consuming to implement, and gaps remain in the list of available DNA binding targets. Zinc Finger Historical Timeline 1985 1991 1995 1996 2000 2004 2008 2009 2011 iGEM '11 2011.igem.org/Team:Harvard/Human_Practices
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Post by skyship on Mar 5, 2014 20:07:29 GMT -5
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Post by skyship on Mar 5, 2014 21:41:51 GMT -5
So, those experimental ZFNS? Does that mean open global field petri dish? that would still qualify under the non disclosure items. Well, but, what about the open experiments themselves. For gene therapy only or dump in environment and see what it can do? The Primordial ooze protocell, protomolecule delivered to the environment in their so called experiments. Even govt approved ...and what ever else .....in the Aerosol operations document.
So, my question is, was the ZFN used for the RNAi the ncRNA, or snoRNA, or the SRNA or smRNA all involving the tRNA. ncRNA is supposedly all over the environment, now.
So any connections there?==================== ZINC FINGER 1, 2, 3 Epidemial growth factor??Astrocytes?
Epidermal-growth-factor-induced proliferation of astrocytes requires Egr transcription factorsjcs.biologists.org/content/122/18/3340/F7.expansion.html--------------------------
Are these the Editosomes? RNAi the editor? or ZFN? Hence the deformed Euglena organism in us? Shape looks like a trypanasome to me. Did they use all four from T. Bruceii, Leishmania etc? www.jbc.org/content/286/22/19320.short========= www.landesbioscience.com/resized_cover/400/books/Iuchi.jpgwww.landesbioscience.com/books/iu/id/900/?nocache=1198827067
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Post by skyship on Mar 5, 2014 22:39:26 GMT -5
The cobalt ferrite nanoparticles fired at temperature 800°C; show the highest saturation magnetization while the zinc ferrite nanoparticles coated with silica shell shows the highest diffuse reflectance. On the other hand, core/shell zinc ferrite/silica nanoparticles fired at 400°C show a ferromagnetic behavior and high diffuse reflectance when compared with all the uncoated or coated ferrites nanoparticles. These characteristics of core/shell zinc ferrite/silica nanostructures make them promising candidates for magneto-optical nanodevice applications. Keywords: nanostructures; oxides; cobalt ferrite; cobalt zinc ferrite; zinc ferrite; magnetic properties; diffuse reflectance. www.nanoscalereslett.com/content/6/1/460================================= Since these show reflectance the could be plasmon resonance nanoparticles. Again, the video from "plasmon resonance .." thread by aqt.... and the nanoparticles: Here there are plasmon resonant nanoparticles. an explanation..... www.youtube.com/watch?v=1-LyEHp0GIM
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Post by kritters on Mar 10, 2014 22:03:22 GMT -5
Well, this Ormus and m-rodium is BA-LOWING MY MIND!!! First, thanks for tolerating me here. I'm like a fly on the wall drop-jawed and so appreciative of all this incredible knowledge and information. I feel like the little yippie mascot jumping up and down and asking about things I don't understand! Hopefully I am providing some light distraction for some well deserved mental breaks. I have never heard of this! Evidently, this Ormus thing is fairly new conceptually? Sky, weren't we talking on this forum a long while back about the dead sea? Is this how it's significant? Also, I'd like to back up a bit and ask a seemingly stupid question: who was it that had the idea to use the wine swish and spit test for Morgs? What made him/her think to try this? I mean, did someone get really drunk on wine one night and spit in the sink and see the Morg strings and say, Ureka, what a great test! ? Reason I ask is that I'm wondering if anyone tried using sugar and blue food coloring to swish. I'm wondering if it's the sugar in (did they use cheap, sweet wine in which sugar was added?) the wine that lured the critters out of the teeth, gums and tongue and the red wine just stained it. I'm thinking, on an aside, that the most effective treatments might be a combination of sugars for feeding frenzy and then a solution to trap and kill the suckers. Like what I just did in my mouse traps. Also, does anyone know if wine is made from seeded or seedless grapes? I would assume the quality wine would come from grapes with seeds intact. I go to whole foods to buy grapes with seeds so I can get the benefits, although I usually stay away from fruit because of my candida. But I figure, while I eat some of them, the grape seed extract might kill them. Thus my theory on the trap and kill LOL. Also the bioflavinoids in the grape skins, which are used to make red wine. How would they come into play? Anyway, thanks for that info you all seem to take in stride about Ormus. That is an amazing and seemingly untapped source for important health information. Best, Kritts
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Post by kritters on Mar 10, 2014 22:04:10 GMT -5
"...Also, I'd like to back up a bit and ask a seemingly stupid question: who was it that had the idea to use the wine swish and spit test for Morgs? What made him/her think to try this? I mean, did someone get really drunk on wine one night and spit in the sink and see the Morg strings and say, Ureka, what a great test! ? Reason I ask is that I'm wondering if anyone tried using sugar and blue food coloring to swish. I'm wondering if it's the sugar in (did they use cheap, sweet wine in which sugar was added?) the wine that lured the critters out of the teeth, gums and tongue and the red wine just stained it. I'm thinking, on an aside, that the most effective treatments might be a combination of sugars for feeding frenzy and then a solution to trap and kill the suckers. Like what I just did in my mouse traps..".
Can someone answer this?
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Post by skyship on Mar 13, 2014 10:54:04 GMT -5
I believe the swish test came from Dr. Gwen Scott.
But, It is the grape in the wine. It is fermented. But, I use grape juice, you get big strands out.
The organism I believe has the same frequency as the Morgellon's Organism.
S
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Post by skyship on Mar 13, 2014 11:19:02 GMT -5
Cell like Systems: This involves creating a "minimal cell" or recreating the LUCA. Just like the Big Bang, the desire to recreate it at Cern, the desire to recreate the "Last Universal Common Ancestor" or LUCA, however cell like systems are being created. One group worked on organic chemicals (protocells) the other worked on minimal cell, and thirdly they put them together, to create a biological machine that could interface with nano.
Mimic life, with "defined components"Different approaches to building new, artificial cells. Typically, laboratories either begin with chemicals (left) or an existing cell (right). Presumably an approximation of the last universal common ancestor (LUCA) exists in between these two extremes. A third approach is to piece together cellular systems from existing biological components (bottom). www.ncbi.nlm.nih.gov/pmc/articles/PMC3856425/figure/F1/
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Post by skyship on Mar 13, 2014 11:28:08 GMT -5
www.researchgate.net/publication/256426331_Piecing_Together_Cell-like_SystemsAre we witnessing the "bottlenecks" Bundles? "molten globules"? aggregration? Cell free genetic circuit assembly: ABSTRACT Cell-free genetic circuit elements were constructed in a transcription-translation extract. We engineered transcriptional activation and repression cascades, in which the protein product of each stage is the input required to drive or block the following stage. Although we can find regions of linear response for single stages, cascading to subsequent stages requires working in nonlinear regimes. Substantial time delays and dramatic decreases in output production are incurred with each additional stage because of a bottleneck at the translation machinery. Faster turnover of RNA message can relieve competition between genes and stabilize output against variations in input and parameters. www.researchgate.net/publication/9050157_Principles_of_cell-free_genetic_circuit_assembly
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Post by skyship on Mar 13, 2014 11:36:06 GMT -5
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Post by skyship on Mar 13, 2014 11:46:25 GMT -5
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Post by skyship on Mar 13, 2014 12:10:31 GMT -5
Now, is this to be used in the lab only? or is it being used in connection with creating these biological units to be used in Universal applications. Man one with the earth? They are libraries right now, but are those libraries to be on chips? like your medical history on a "lab on a chip library"? and your soon to be bank account? Is this cell free system what is in our Extracellular spaces, connective tissues etc. Translation bundles, are those the rna polymerases tangling as unfolded proteins? Traveling through pores? like tau all over the bod? In order to be proteins, amino acid chains have to be folded; the Never Born Proteins (NBP) project is directed toward the discrimination between folded and unfolded chains in a random ensemble of synthetic polypeptides. The approach involves a “total randomization” with no bias toward any given structural or functional property, leading almost necessarily to novel proteins not present in nature, the NBP (Chiarabelli et al., 2006b; Luisi et al., 2006a). ..". The experimental procedure developed to pursue this goal is based on the concept that folded polypeptides are more protected against digestion by a protease than unfolded ones. The first attempts to combine a library-production method with the selection of folded protein by proteolysis belong to Kristensen and Winter’s (1998). In that case the starting point has been the selection of variants with improved properties from known extant proteins. The originality of our procedure, with respect to literature, lies in the library itself, being made by de novo completely random sequences not present in nature and in the insertion of a specific short fixed sequence within a total random polypeptide sequence to create the library. Such short sequence is specifically recognized, so that folded peptides have less chances to be enzymatically digested than unfolded ones. The NBP selection method links the proteolytic resistance with the selective recovery, useful to get new folded peptides (Figure Figure11). With our approach, a library of 50 residues long random peptides has been produced and screened (Figure Figure11, bottom), and the work demonstrates that the selection of folded random proteins is feasible (Chiarabelli et al., 2006b, 2009, 2012; Luisi and Chiarabelli, 2011)"........ www.ncbi.nlm.nih.gov/pmc/articles/PMC3779815/fig 1. www.ncbi.nlm.nih.gov/core/lw/2.0/html/tileshop_pmc/tileshop_pmc_inline.html?title=Click%20on%20image%20to%20zoom&p=PMC3&id=3779815_fmicb-04-00285-g001.jpg
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Post by skyship on Mar 13, 2014 12:20:43 GMT -5
The NSF project: EMERGENT BEHAVIOR OF INTEGRATED CELLULAR SYSTEMS: AN ENGINEERING APPROACH TO THE DESIGN OF BIOLOGICAL MACHINES OUR GOALS ́ To understand the complexities of integrated cellular systems so that we can ultimately instruct cell populations to develop into unified functional machines To educate a diverse generation of students well-versed in the new biology ́ To inform and educate industry and the general public of the enormous potential for biological machines www.nsf.gov/od/iia/programs/stc/newdirectors2010/EBICS.pdf
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Post by skyship on Mar 13, 2014 12:33:10 GMT -5
Semi-synthetic minimal cells. (A) Semi-synthetic minimal cells are based on the encapsulation of the minimal number of biological molecules, like DNA, ribosomes, tRNAs, enzymes, amino acids, nucleotides, etc., inside lipid vesicles. Currently it is possible to encapsulate the whole transcription–translation machinery so that proteins are synthesized inside the synthetic cell. The goal of research is the self-reproduction of the minimal cells thanks to the simultaneous (and possibly coupled) production of internal and membrane components. Reproduced from Chiarabelli et al. (2009) with the permission of Elsevier. (B) Confocal fluorescence image of a liposome, prepared by the droplet transfer method, which contains the whole transcription–translation machinery (E. coli cell extracts) for producing a protein from the corresponding DNA sequence. In this case, the enhanced green fluorescence protein (eGFP) was synthesized, as evidenced by the green fluorescence. (C) The liposome membrane were made visible after Trypan blue addition, which binds to phospholipid bilayers and becomes red fluorescent upon 543 nm excitation. (D,E) Quantitation of fluorescence along the yellow lines in (B,C) gives typical bell-shaped and U-shaped profiles, respectively, for water-soluble (eGFP) and membrane-bound (Trypan blue) fluorochromes. www.ncbi.nlm.nih.gov/pmc/articles/PMC3779815/figure/F2/
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Post by skyship on Mar 14, 2014 0:48:45 GMT -5
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Post by skyship on Mar 14, 2014 1:35:26 GMT -5
What we are dealing with are synthetic parts (from other proteins, genes, other biological entities) and chemical creation on the other side. But, this is pretty clear on one of the subjects.
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Post by aqt on Mar 16, 2014 12:04:10 GMT -5
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Post by skyship on Mar 19, 2014 1:33:05 GMT -5
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Post by skyship on Mar 24, 2014 15:00:10 GMT -5
For the most part, I have come back where I started, just trying to understand the process of "The Art" or the "The Great Work". It appears that this happens at the beginning of a new so-called "Renaissance". You can see what is about to happen, but, was it done in a "good way" or only to sway as the previous one did. You can see the pattern. However, what went seriously wrong this time? The first stage? There are four stages. One can look at this in physical consequences, mental and emotional, spiritual, economically, politically, and health wise. It is all covered in this "Great Work". Note the four stages, in the second link:================================= 1. en.wikipedia.org/wiki/Great_Work================================= =================================== Nanotech: a new paradigm, a new science, a new "Renaissance". the error was at the first stage: Melanin as indicated by Nicolaus. There is natural and synthetic melanin. Acetylene and pyrroline: oligomers insoluable oligomers, amyloids, unfolding of basis of life and folding in a new life, of sorts on a self assembling basis. The goal: Transformation, transmutation, transference, trans.....tRNA with messenger RNA: mRNA etc, noncoding RNA: ncRNA. etc....... Melanin is in outer space, hydrocarbons, PAHs, buckyballs etc. One can see the links. When does Magic become science and science Magic?================================ ================================== Since when is Melanin a putrid factor? Matter is in all things.================== ========================== ======================= ===================== ============================== So, black, white, yellow and red. In Google terms: Blue, Red, Yellow and Green. So recording the physical reactions to this process. Melanin the beginning of this process: the quiding RNA strand (black). This was and is a process without our consent or knowledge, because the knowledge was and is kept from us, as always. But, why would we be rejecting these? We are Awake to the process and the core of it's process, yet we cannot find the elements used. That is because they are not of this crust, the earth. Stardust and rare metals, compounds, etc.....as in the days of the so-called gods~!
Many are uncovering this so called nano, magic, science. When one looks at the patents for this new science, one sees that whoever is going for the patent, has to be educated in "The Art". The Alchemical Art. And will direct those under them to compartmentalize their part in the "Great Work", but, will not inform them of what is to be done with their part~!======================= Our part, is to expose what they have done, so we at least have an idea of what is wrong with us, thereby find ways to see beyond what has control over us, and freedom resides in this knowledge as well. For we are "individually made", not "unitarianized" or "universal" all one hive, as is desired. We have our own histories~! We know who runs the earth~! and all it's genes and elements~! and it has been loosed for a time~!------------------------------ So, the essence of life, can be tampered with, we now know, but, the spirit of life, is still there and here, we feel it, we see it, we hear it, we smell it, we speak it. When melanin switches, it sparks, according to Nicolaus.
What is the "wrong" switch? What is the "right" switch?
more on this later.
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Post by skyship on Mar 24, 2014 15:47:27 GMT -5
More on how melanin studies were mis directed: physically and functionally: The Polymer.
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Post by skyship on Mar 24, 2014 22:05:54 GMT -5
Here are the alchemical elements symbols. How are they used today in the nanoworld? or nobel metals found under crust, hydrovents: extremophiles etc.3.bp.blogspot.com/_pFD3voOGUZ4/SMrGnhZcdVI/AAAAAAAAADg/GnQy7zgZLYs/s400/Dalton_atomic_symbols.jpgI would not get into the process unless you understand it. These are used though by top scientists today. Could they be wrong in use of some of them? Maybe? Or they enjoy the magic of it all. Rather than the true science and since the "common folk" don't know the true alchemy, how would (we) know if it was wrong? or intentionally wrong. Or intentionally for a purpose? We wouldn't. But, when it comes to our personal selves and health, we have every right to know~!
Where I am going with this, "The Great Work", is into Genetics, involving nano. So, has this been tried every 500 years or so? Or is it ongoing to a final tranformation? transhumanism? or the next industrial age, created, called "The Singularity"? Does this mean people are singled out? Does it have multiple meanings?
If molecules and molecular machine was the mistake, how can we be certain the nanodevice or nanomachine inside the human body is legit, or safe or not a spy device, film, or recorder? How can we determine if the filaments are not the device now? or the melanin particle? Can it be programmed? Was it?
====================== Has nano corrected the molecular problem with melanin?
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Post by skyship on Mar 24, 2014 22:22:24 GMT -5
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Post by skyship on Mar 24, 2014 22:41:35 GMT -5
Identification of Partially Degraded Oligomers of 5,6-Dihydroxyindole-2-carboxylic Acid in Sepia Melanin by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry--------------------------------------------- Melanin is a polymer, so it would have been easy to make a mimic of this melanin polymer, that would be the oligomer polymer. Acetylene, pyrroline, sepia, making it synthetic by using from other animals. But, would not be human. Cannabalism comes to mind, if eating human brains was pagan, and pagan is running the show, well then, we know where a lot of melanin would be. Is this the importance of the "skull"? Not the bone matter, but what was taken from it. Have we resorted to this? the particle melanin or the molecular melanin? i32.photobucket.com/albums/d25/GoldenMenes/factpath.gif
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