71 - World of the Micro y Macro Cosm

Life is that what recombined, re-created, changed all the elements of the Universe (Byronic Matter) at atomic scale atom by atom - into double helix living structures. Called the replication of the DNA molecule - “The very first thing that embryonic stem cells do, without any effort at all, is that they make neurons,” our cell make up reflect the presence of multiple organisms working together in harmony

a human cell contain up to 1500 mitochondria energy sources

from microbial origins - Bio-Logica

it is also good to know every spermatozoon

DNA double helix molecule

is impulsed by one of these, with a tail to steer on a pheromone trail following a calling sign from a beacon in space . A dark force is that power, that brings matter under control - the dark controlling force - is a life force - as life is a form of intelligent energy - created out of the matter of the Universe - We are all children of light and star dust - As all we eat comes from the sun - all the biomass we consume derive its assembly and energies from Inti.

Also good to know that the red color of our blood is from iron atoms, formed in super nova stellar explosions

but now, intelligence can exist without this Sun-God-Inti or call him Aten if you wish

Man have entered the era of light, insight and vision, to see and make his future very clear

“Reality isn't a thing or static place,”

“It’s a Biological process.”

Bio-Logica.

The very first thing embryonic mother cells do,

without any effort at all "Wu Wei"

they make neurons for communication

“They are assembling basically the building blocks of reality.

If you look at embryonic stem cells, or the Ants

they can do everything - just like us, every cell of the body is inter connected to communicate

with what we call neurons, pheromones, just like words - it is about the right vibration, intonation and sequence of command

As we do on the Internet - Now I am talking to you.

The laws of physics and chemistry can explain the biology of living systems, in detail. Right down to the

chemical foundations and cellular organization of Bio-Cells,

it is all about Bio-Logica:

oxidation, biophysical metabolism, the carbohydrates and amino acid patterns.

Every living creature is the center of

his own Aura and reality.

In fact, space and time fall into the realm of Bio-Reason

as animal sense perception - not of physics.

They are properties of the mind,

Consciousness cannot exist without a living creature

Life embody its perceptive powers of creation.

Therefore we must turn to the logica of Life,

to Bio-Logica,

if we are to understand the world around us.

Is to see the reflected light from the living

The Macrocosm mirror the Microcosm

The spinning atoms in Hafnium Carbide Crystals

"lock in resonance together"

in the same stable geometric shape as the face of the crystals.

I think the word is to resonate in harmony.

The light of knowledge, enlighten the dark matter.

See the magic world of the Living.

All Life with the Double Helix structure is the sacred creator of all.

It is within human capacity

to gain control, and flip-flop Photons and Electrons

where we want them to be. At speeds of 100gigas/sec.

To gain control of everything in the abstract realm is Bio-Logica

within our star-ship Helios.

Meaning all that dark uncontrolled asteroids floating out there as indicated in image below on the right.

In control of all the Mass - meaning to be in control of all the kinetic energy and apply to our advantage as logica indicates.

Must be under control and directed to our advantage.

Intelligent Objective Reason

must Re-Create the whole order of the Universe by Bio-Logica

Synchronize movement to create order in harmony.

Like cosmic music - echo in our IDREA.

Where it is noble to be creators in resonance.

Intelligent Reason is the Logica to indicate where everything should go.

Intelligence is seated here on mother earth from where it will expand into alternative life forms of our making.

To explore the Universe as if with our own eyes -

looking deeper into visual time, under our control.

Light is life's energy and reflected light a visual source for memory

Intelligence is know how to interpret all detail in that visual world.

Have insight into the whole story

which is the scope and extend of all reflected light.

We are children of light

it is the essence of everything we eat entwined in the DNA of our genetic make-up.

Reflected light spin energy is the content of this memory.

It is all about vision - connected at the speed of thought.

The constellation of all proteins in a cell is called its proteome. Unlike the relatively unchanging genome, the dynamic proteome changes from minute to minute in response to tens of thousands of intra -and extracellular environmental signals.

A protein's chemistry and behavior are determined by the gene sequence and by the number and identities of other proteins made in the same cell at the same time and with which it associates and reacts. Studies to explore protein structure and activities, known as proteomics, will be the focus of much research for decades to come and will elucidate the nutrient-sensing systems, molecular basis of health and disease.

The DNA in each human cell is packaged into 46 chromosomes arranged into 23 pairs. Each chromosome is a physically separate molecule of DNA that ranges in length from about 50 million to 250 million base pairs. A few types of major chromosomal abnormalities, including missing or extra copies or gross breaks and rejoining (translocations), can be detected by microscopic examination. Most changes in DNA, however, are more subtle and require a closer analysis of the DNA molecule to find perhaps single-base differences.

Each chromosome contains many genes, the basic physical and functional units of heredity. Genes are specific sequences of bases that encode instructions on how to make proteins. Genes comprise only about 2% of the human genome; the remainder consists of non coding regions, whose functions may include providing chromosomal structural integrity and regulating where, when, and in what quantity proteins are made. The human genome is estimated to contain some 25,000 genes.

Basics on DNA Research.Over the next decade, as molecular biologists tackle the task of sequencing the human genome on a massive scale, any number of innovations can be expected in mapping and sequencing technologies. But several of the central tools of molecular genetics are likely to stay with us -- much improved perhaps, but not fundamentally different. One such tool is the class of DNA-cutting proteins known as restriction enzymes. These enzymes, the first of which were discovered in the late 1960s, cleave double-stranded DNA molecules at specific recognition sites, usually four or six nucleotides long. For example, a restriction enzyme called EcoRI recognizes the single-strand sequence GAATTC and invariably cuts the double helix as shown in the illustration futher down on the left.

When digested with a particular restriction enzyme, then, identical segments of human DNA yield identical sets of restriction fragments. On the other hand, DNA from the same genomic region of two different people, with their subtly different genomic sequences, can yield dissimilar sets of fragments, which then produce different patterns when sorted according to size.

In classical gel electrophoresis, electrically charged macromolecules are caused to migrate through a polymeric gel under the influence of an imposed static electric field. In time the molecules sort themselves by size, since the smaller ones move more rapidly through the gel than do larger ones.

In 1984 a further advance was made with the invention of pulsed-field gel electrophoresis, in which the strength and direction of the applied field is varied rapidly, thus allowing DNA strands of more than 50,000 base pairs to be separated. A third necessary tool is some means of DNA "amplification." The classic example is the cloning vector, which may be circular DNA molecules derived from bacteria or from bacteriophages (virus like parasites of bacteria), or artificial chromosomes constructed from yeast or bacterial genomic DNA.

A yeast artificial chromosome, or YAC, for instance, is constructed by assembling the essential functional parts of a natural yeast chromosome -- DNA sequences that initiate replication, sequences that mark the ends of the chromosomes, and sequences required for chromosome separation during cell division -- then splicing in a fragment of human DNA. This engineered chromosome is then reinserted into a yeast cell, which reproduces the YAC during cell division, as if it were part of the yeast's normal complement of chromosomes. The result is a colony of yeast cells, each containing a copy, or clone, of the same fragment of human DNA. One of the important achievements of the Human Genome Project has been to establish several libraries of such cloned fragments, using several different vectors (bacterial artificial chromosomes, P1 phages, and P1-derived cloning systems), that cover the entire human genome.

Another way of amplifying DNA is the polymerase chain reaction, or PCR. This enzymatic replication technique requires that initiators, or PCR primers, be attached as short complementary strands at the ends of the separated DNA fragments to be replicated. An enzyme then completes the synthesis of the complementary strands, thus doubling the amount of DNA originally present. Again and again, the strands can be separated and the polymerase reaction repeated -- so effectively, in fact, that DNA can be amplified (replicate) by 100,000-fold in less than three hours.

When a clone library can be ordered -- that is, when the relative positions on the human chromosomes can be established for all the fragments -- one then has the perfect resource for achieving the project's central goal, sequencing the human genome. How the sequencing is actually done can be illustrated by the most popular method in current use, the Sanger procedure, which is depicted schematically above. The first step is to prime each identical DNA strand in a preparation of cloned fragments. The preparation is then divided into four portions, each of which contains a different reaction-terminating nucleotide, together with the usual reagents for replication. In one batch, the replication reaction always produces complementary strands that end with A; in another, with G; and so on. Gel electrophoresis is used to sift the resulting products according to size, allowing one to infer the exact nucleotide sequence for the original DNA strand.