Activation of anti-aging gene Klotho

Synthesit almost doubles the activation of anti-aging gene Klotho. Scientific studies have shown that the genetic mechanism of Synthesit action maintains overall health and prolongs youth
Anti-age
Hair & nails
Immunity

The latest sensational research findings have proven our hypothesis to be true that the bioactive Synthesit mineral works at the genetic level as well promoting (activating) Klotho gene expression by 1.9 times.

In vitro research was conducted at the Federal Research Center of Fundamentals of Biotechnology.

It has been scientifically proven that Klotho gene expression contributes to the normalization of growth hormone (GH) production, prevents the aging of the body and the development of impaired glucose tolerance (type 2 diabetes mellitus), cerebral blood flow impairment and coronary heart disease. The Klotho gene also promotes B-cell differentiation and prevents the development of osteoporosis.

The graph below shows an increase in the activity of the Klotho gene when the use of Synthesit. This is a phenomenal result. This action has no analogs.

The beneficial effect of Synthesit action on the Klotho gene is another complement to the previously obtained scientific data that Synthesit increases the number of stem cells by 2.45 times (Increasing the number of stem cells), helps to reduce age-related values of blood biochemistry up to 40% (Alt, Ast, Cholesterol levels), suppresses the growth of cancer cells (Oncology and experiments on monkeys), reduces the activity of "harmful" Adenosine Deaminase and Xanthine Oxidase enzymes (Health recovery research), thereby protecting cells from destruction, counteracting free radicals and promoting tissue respiration.

The study was performed by Darya Kaplun, Jr. Scientist, Biology at the Federal Research Center of Fundamentals of Biotechnology.

Read the full scientific research document below:

Liver tissue of a typical histological structure

(hematoxylin and eosin coloring, x400 scaling)

Myocardial tissue of a typical histological structure

(hematoxylin and eosin coloring, x400 scaling)

Kidney tissue of a typical histological structure

(hematoxylin and eosin coloring, x400 scaling)

Lung tissue of a typical histological structure

(hematoxylin and eosin coloring, x400 scaling)

Bone marrow of a mouse not taking iron citrate

(hematoxylin and eosin coloring, x400 scaling)

Bone marrow of a mouse taking iron citrate

(hematoxylin and eosin coloring, x400 scaling)
THE CONTROL

A smear imprint of the bone marrow of a mouse not taking iron citrate

(May-Grunwald-Giemsa coloring, cytological micropreparation, scaling x400)
THE EXPERIMENT

A smear imprint of the bone marrow of a mouse taking iron citrate

(May-Grunwald-Giemsa coloring, cytological micropreparation, scaling x400)
THE CONTROL

A smear imprint of the bone marrow of a mouse not taking iron citrate

(May-Grunwald-Giemsa coloring, cytological micropreparation, scaling x1000)
THE EXPERIMENT

A smear imprint of the bone marrow of a mouse taking iron citrate

(May-Grunwald-Giemsa coloring, cytological micropreparation, scaling x1000)
INDICATORS
CONTROL GROUP
EXPERIMENTAL GROUP
Total myelokaryocyte amount (on the thigh),mln
15,0 ± 0,9
*22,2 ± 1,2
Reticular cells
1,3 ± 0,1
*1,5 ± 0,1
Non-deferred blasts(monocular cells)
2,2 ± 0,1
*5,4 ± 0,1
Myeloblasts
2,1 ± 0,1
*3,5 ± 0,1
Myeloid cell mitosis
0,1 ± 0,0
*0,2 ± 0,0
Lymphocytes
16,8 ± 1,8
*22,0 ± 1,1
Megakaryocytes
0,3 ± 0,0
*1,1 ± 0,1
Erythroblasts
0,5 ± 0,1
*1,9 ± 0,1
*statistically significant difference compared with the control group.

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