Tom2004
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- May 19, 2019
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Seeing as there is no chance of growing naturally, I will inject BMP-7 into the knee joint so I can grow
Need sources tho..
Need sources tho..
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How much generic HGH is enough for significant growth. I’m talking like IGF-1 levels above 800ng/mLJesus, good luck.
also enjoying spending like $5000 monthly for this shite, also good luck finding a source that is actually legit.
firstly, a childs IGF-1 is through the fucking roof, my baseline was 486ng/dl at 17 years old, even before I took peptides it was high. after my peptide protocol, my IGF-1 was beyond 800ng/dl, insanely high. I'm taking 7.5iu's daily of puretropin from ironlionlabs, I'm getting intense side effects that all GH users experience.How much generic HGH is enough for significant growth. I’m talking like IGF-1 levels above 800ng/mL
does anything work at 20?firstly, a childs IGF-1 is through the fucking roof, my baseline was 486ng/dl at 17 years old, even before I took peptides it was high. after my peptide protocol, my IGF-1 was beyond 800ng/dl, insanely high. I'm taking 7.5iu's daily of puretropin from ironlionlabs, I'm getting intense side effects that all GH users experience.
I'd assume my IGF-1 is in the 850-900ng/dl range. I don't think it can go any higher without the usage of IGF-1 DES or LR3 as your liver can only convert at a certain rate and most of the GH will be metabolized before it can convert to IGF1.
my source costs approx $928AUD for 53 days at 7.5ius, I'm going to taper down to 5ius daily, this will make the growth hormone last around 80 days.
and does that even work or is that just a cope? any sides?BMP-7.
thats all.
I don't know anything about it tbhand does that even work or is that just a cope? any sides?
Can an oldcel get benefits from using hgh?I don't know anything about it tbh
all I know is that it's insanely expensive, hard to source and mostly cope.
Bro how old are you and did you grow with your protocol?firstly, a childs IGF-1 is through the fucking roof, my baseline was 486ng/dl at 17 years old, even before I took peptides it was high. after my peptide protocol, my IGF-1 was beyond 800ng/dl, insanely high. I'm taking 7.5iu's daily of puretropin from ironlionlabs, I'm getting intense side effects that all GH users experience.
I'd assume my IGF-1 is in the 850-900ng/dl range. I don't think it can go any higher without the usage of IGF-1 DES or LR3 as your liver can only convert at a certain rate and most of the GH will be metabolized before it can convert to IGF1.
my source costs approx $928AUD for 53 days at 7.5ius, I'm going to taper down to 5ius daily, this will make the growth hormone last around 80 days.
Why lose a limb?The chances of you acquiring legit bmp-7 and injecting it without losing a limb, all while being able to spend 5000$/month on it are pretty negligible tbh.
https://www.ncbi.nlm.nih.gov/pubmed/9599038Quote:OBJECTIVE:
In a recent study, we demonstrated that mesenchymal stem cells (MSCs) derived from the synovial membranes of bovine shoulder joints could differentiate into chondrocytes when cultured in alginate. The purpose of the present study was to establish the conditions under which synovial MSCs derived from aging human donors can be induced to undergo chondrogenic differentiation using the same alginate system.
[...]
RESULTS:
BMP-2 induced the chondrogenic differentiation of human synovial MSCs in a dose-dependent manner. The response elicited by BMP-7 was comparable. Both of these agents were more potent than TGF-beta1. A higher level of BMP-2-induced chondrogenic differentiation was achieved in the absence than in the presence of serum. In the presence of dexamethasone, the BMP-2-induced expression of mRNAs for aggrecan and type-II collagen was suppressed; the weaker TGF-beta1-induced expression of these chondrogenic markers was not obviously affected.
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However, this doesn't matter because:Quote:The objective of this study was to examine in vitro the influence of recombinant human osteogenic protein-1 [rhOP-1, or bone morphogenetic protein-7 (BMP-7)] on cartilage formation by human and goat perichondrium tissue containing progenitor cells with chondrogenic potential. Fragments of outer ear perichondrium tissue were embedded in clotting autologous blood to which rhOP-1 had been added or not added (controls), and the resulting explant was cultured for 3 weeks without further addition of rhOP-1. Cartilage formation was monitored biochemically by measuring [35S]-sulphate incorporation into proteoglycans and histologically by monitoring the presence of metachromatic matrix with cells in nests. The presence of rhOP-1 in the explant at the beginning of culture stimulated [35S]-sulphate incorporation into proteoglycans in a dose-dependent manner after 3 weeks of culture. Maximal stimulation was reached at 40 microg/mL (human explants: +148%; goat explants: +116%). Histology revealed that explants treated with 20-200 microg/mL of rhOP-1, but not untreated control explants, contained areas of metachromatic-staining matrix with chondrocytes in cell nests. It was concluded that rhOP-1 stimulates differentiation of cartilage from perichondrium tissue. The direct actions of rhOP-1 on perichondrium cells in the stimulation of chondrocytic differentiation and production of cartilage matrix in vitro provides a cellular mechanism for the induction of cartilage formation by rhOP-1 in vivo. Thus rhOP-1 may promote early steps in the cascade of events leading to cartilage formation and could prove to be an interesting factor in the regeneration of cartilage in articular cartilage defects.
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