2mg/Vial Peptides Hormone AOD-9604 for Fat Lossing
AOD9604 Basic Info.
Model NO.:CAS: 221231-10-3
Synonyms:Fragment 177-191, Aod-9604
Packing:According to Every Customers′s Requirements
Standard:SGS GMP ISO
Grade : Pharmaceutical Grade
Storage: Closed, below 2 ~ 8oC preservation
Related substance: Total Impurities(%) ≤ 2.0%
Acetate content: ≤ 15.0%
Bacterial Endotoxins: ≤5 IU/mg
Reduces the most stubborn abdominal fat.
Increases muscle mass
Increases IGF-1 levels, in an effective manner, thus making this a
peptide that burns fat
Increases energy expenditure
Improves lipid profiles and lipolytic activity does not negatively
impact blood glucose level, nor does cell proliferation occur, like
Human Extremely potent and effective fat burner.
fragment 176-191 is an analog of the -releasing factor (GRF) which
signals the effects of . It is a 15-mer peptide residue of the
C-terminus of to which tyrosine is added at the N-terminal end.
This synthetically produced hormone is very common to weightlifters
and bodybuilders because of a number of physical benefits. Studies
claimed that it actually acts on the reduction of excessive adipose
tissues such as those in the abdominal area, increase in muscle
mass, and enhances the lipid content of the body.
These segments of the synthetic peptide AOD9604 have been
researched for their in vivo effects in laboratory mice musculus.
Results have shown that AOD9604 have resulted to a short-period
increase in blood glucose and a more sustained increase in plasma
insulin, together with other fragments such as 172-191, 177-191 and
In addition, the researchers have suggested that functionality of
the peptide depends not only in the informational sequence but
should also have the correct physical configuration (Ng and
Borstein 1978). Also, AOD9604, being a region of high accessibility
to proteases and also rich in proline, have been demonstrated to
affect the conformational change in the cytoplasmic domain of the
band 3 of erythrocyte membrane protein by serving as the hinge for
the pivoting of the two subdomains. This then suggest that such
residue is significant in conformational changes be serving as
sites for peripheral protein binding in some body cells (Low et al.
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