This diagram shows the blueprint of a sump column of the Micellar Morpholograph,

designed to separate unnecessary lighter mass from heavier mass but reduce heaviest
calcified proteins to make way for glycolipid derived class of protein. Levitation and density
function together for synthesising the ‘backbone’ of the micelle cultivation.
Heat convection current ‘[-H,RT] = 40(-10^-2)’ in the chamber of a Micellar Morpholograph.
This is a dissection of the Micellar Morpholograph, labelled suggestions of what species of
chemical are needed to manipulate with. The position of the miscible slit (where the
spheres reside in the upper column) are inflicted with ‘Gravitation induced pressure’ an
upward downward compressive forces the membrane to accept passive electrical impulses
that leave dissipated heat spread over the membrane at different strengths according to
lower(low strength), higher(high strength) this keeps the ‘wheel turning’ on the micelle
ensuring envelop consistency and a change in envelope

thickness as rate increases.

This Diagram is the top view excluding the column and we call this the chamber of the
Micellar Morphologram. It is the start process and the end process for the micelle. The
striated plane is a high heat zone. Each bend competes with high acceleration. This rat out
the under formed micelle from the fully formed micelle. We test synthetic oocyte quality
through dispensing some fluid from the left or right side as they have equal acceleration
path lengths.
This is a dissection from a dissection, the Magnetic pulses give us structural path lengths so
that the convection pathway is following a common ‘normal’ direction. Not fully understood
and hard to apply in real life. This could change the behaviour of kinetic flow and
experiential mass accumulation. There are two poles that are different much like a circuit
without a control port. Hosting a sameness, must remember that it is the medium
generating this pathway over glow.
A rough guide to purification of mixture is maybe applying sponge materials in
chromatographic settings. Room temperatures are remaining similar to the more passive
environment and over time this should yield results. Soap water implies the gradual
deposition of the more calcified molecules.
This is a more simplistic view of an important aspect of Liquid Chromatography in general
these columns are shifting and separating molecules for the detection sheets that line the
columns at a column detecting point just after mobile phase.

A
schematic representation of mouse oocyte growth of differing periods in time. mRNA a
signal that is very important, detected at vast quantities. Located in the GV, geminal vesicle.
Picture from UNSW lead research teams, wiki.
Enveloper
Carbon-carbon body (two-
Way movement)
Cholesterol
Water + Silica based
Allergens sensitivity
Emulsifier (Attractant)
Charger
Phosphorus (volatile)
Ferrous-chelates DNA
coated
Water + Amines
“Energy Acceptor” (builder)
Enforcer
Lipid bilayer (oil)
Cyclo-organic molecules
Non-amine groups. Egg
sample/immune specified
broth
Oil
Attachment (building block)

Materials categorised that are roughly in the order they are in real life. To create a 360 angle
spheroidal non-inverse shape at best.

This fractioning column divides, separates and changes the state using hot and cold. It is
used for the most elemental ionic and primordial natures. Sound Is a nice replacement for
heat.
Gel Testing an added tool to be use for a very complicated investigation into superposition
of sub particle background periodic charge reducing fast activity and motility a deep
dissection garnered from the micellar morpholograph. We see a descending wave oscillation
frequency that is irregular as the pulse weakens toward midway to reaching the other side
more-so as the gel expands we see oscillation be guided to different directions. Hydrates in
gel homogenize current and gel is transforming as the charge moves through it. We can only
really expect erratic results when gel is in a fixed air composition ratio reformed container
(not air tight).
 This diagram
is a specifically usefully one to keep in mind the cell polarity changes and the need for
magnetism in a medium. Congrats to Schmidt to spreading this crucial informative
illustration. Reactivity in aggregates is our main focus. Loose network forms are the normal
chemical cycles need to be detected somehow so that they embody macroscopic behaviour
for the micellar Morpholograph bigger probing to relay an instant infographic sight-
informed image to a predictable conclusion.
Two step procedure for recombining a micelle (on a volume to mass scale called reaching a
net value) in which I keep calling homogeneity.
Tried testing the possibilities of the micelle trajectories using a kind of maths that is spatially
dissecting a cells proportional growth. The starting yield tries to stay an average of 2.1nm in
diameter. Some variables change some are stuck in a less formative tone length and stay the
same constant.
Quad partitioning is the stratification of micelle yield in each phase or stage of production.
We are cleansing the chamber of non-uniform product for another participle to take action
but to accompany that we need an environment available to the interface of chemical
inbound substance that have a zero to 2 to 3 quotients for formative use in cell this itself
brings a different kind of energy acceptance a particular binding quotient. Population
statistical data like what we can use for what stage of a process is very non-reactionary
chemically.
The stages that are enforced in the Micellar Morpholograph as a formative device. Around
six or more reactions can accompany this unique cellular cycle. Starting from a broad
estimate of how the network of energy concealment envelopes is to use other cells from the
‘mother’ complex and add this into an ‘energetics’ equation when stage splitting occurs or
endocytosis accepts female acquired mitochondrial organelles.

I am borrowing mathematical techniques of similar arrangement as these two descriptors to

show;
Combinatorial Heat Energy Reaction and below Nuclear Fusion Reaction:

Pab = nanbfab(T)Uab

B = (Zmp + Nmn − M)c2,

We are using size increase as a growth of cell factor for each quartile range disguised as a
stage of times 6 in-between 0.1mm – o.2nm as an indicator of a good Micellar
Morpholograph that gets twisted between two modes. A motif of importance in nano
literature.
This is a illustration of transformative medical theory that explains the transition between
charges over a simpler basic of about [Rn] undescribed region of space that should be
disclosed as a polymorphism exchange region that leaves the semicircle as a constant
“spheroidal” counter parting diagrammatically the region of liquid space, its erroneous
activity is full of incomplete recycled membrane mini ion participants that act as a collective
mop for carbon dioxide, methane and mobile hydrogen users and may or unfortunately so,
adjunct the product in the upper semi-spheroidal as a ethanoate, hydroxide, invites energy
catalyst like zinc(2) (3) open reaction currents. Enantiomers are a cease way chemical
multi-tasking in one chemical that delays certain cycles or rarely bond cycles together. They
are uncommon and toxic in concentration mal-use they are consequently a fixed ratio need.
The chemical [CHO2] is formate and undergoes fast paced electrophilic reactions with lipids
that split off from saponified surfactant end chains that mark endings and starts for sterol
induced lipophile or lyophilic decay. The addition of a polymorphic chains.
The Periodic Table is an elemental index by proton positive and electron negative number
descent. Which also indicates how much mass was procreated to form a stable nucleus to
withstand past and future environments a timeslot game. So, this table gives the false
indication of a static world but it is helpful to retain the human minds vision of what should
be held in memory to be ‘disembodied’ and ‘repurposed’. So, nothing evidently wrong with
everlasting principles as it fosters the later creativity on its human historical continuum.
The Biological table Is an adaption of the sequencing maths used for Q&A questions about
which gene is coded for what protein or what amino acid creates which protein. The Protein
production cycle as I call it. Is the synthesis point that is dependent on more passive modes
of transport and relies on a certain typ
e of linear energy usage?