First Time Order Discount 15% (Code: BEST PEPTIDE)

Search

In Stock

CJC 1295 DAC 10mg

CJC-1295 with DAC is a synthetic peptide, analog of the growth hormone-releasing hormone. Though CJC-1295 without DAC has the same effect and stimulates the production and secretion of growth hormone, the addition of Drug Affinity Complex (DAC) is what increases its half-life allowing it to act longer and more potently.

Research also suggests that CJC-1295 with DAC stimulates insulin-like growth factor 1 (IGF-1) and plays a part in a number of physiological processes.

References:

Alba M, Fintini D, Sagazio A, Lawrence B, Castaigne JP, Frohman LA, Salvatori R. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. Am J Physiol Endocrinol Metab. 2006 Dec;291(6):E1290-4. doi: 10.1152/ajpendo.00201.2006. Epub 2006 Jul 5. PMID: 16822960.

$110.00

CJC-1295+DAC – Peptide Overview

As previously mentioned, CJC-1295+ DAC was developed by ConjuChem Biotechnologies, where the company modified Growth Hormone Releasing Hormone (GHRH), to preserve its benefits while steering clear of the negative effects.

One such modification consists of only the first 29 amino acids of GHRH and is called CJC-1295. Additional effort was then made to prolong its half-life, eliminate some harmful effects, improve its action duration, and generally get a more soluble GH secretagogue, that would be easier to produce in larger quantities, while preserving its effectiveness.

Some might say that CJC-1295 is similar to other GH analogues (such as Sermorelin), but this is not entirely true. Though they are similar, the two peptides differ in structure and mechanism of action.

DAC (drug affinity complex) was added to the original peptide compound to protect it while it circulates the bloodstream. This led to the increased half-life of the peptide and prolonged action.

CJC-1295+DAC – Research, Studies and Potential Effects

Growth Hormone

Numerous lab studies in mice showed CJC-1295 as an effective way of promoting the release of GH. What researchers saw from the studies was the potency of a single dose to increase GH levels in mice by 2 and up to 10 times! What’s even more surprising is that the peak of this GH secretion in mice was reached approximately 2 hours after the administration, and lasted a full 6 days.

Why researchers find CJC-1295 so interesting and worth testing is that its application preserved the normal physiologic GH release. What this means is they were able to see circadian peaks and valleys present in normal GH release cycles. Preserving this rhythm while simultaneously increasing the amount of the hormone in the bloodstream is what’s ensuring minimal side effects and irregularities.

CJC-1295+ DAC studies were able to show its ability to preserve psychological effects GH has on protein synthesis, myocardial function, bone density, blood sugar, lipid metabolism etc, in mice.

Growth

Since CJC-1295 helps maintain normal circadian rhythm and promotes normal GH release, numerous studies in mice showed its potential in normalizing growth issues in mammalian species.

The only limiting factor to its therapeutic application is its short half-life, which is why scientists are experimenting with adding DAC to improve it.

(In)Fertility

Way back in the 90’s, scientists made the connection between ovarian cycle stimulation and ovulation and IGF-1 hormones (as well as the release of GH). Furthermore, an animal study in superovulation proved that the levels of IGF-1 and GH rose significantly during an ovulation.

This leaves an open question as to if administration of CJC-1295 in infertile animal test subjects has the potential to reverse their infertility. Some additional speculations have been made regarding male infertility and CJC’s potential to regulate sperm production. Sadly, by the time of this writing, no such studies have been done, but we’ll be looking forward to seeing them in the future.

CJC-1295+ DAC – Final Conclusion

Numerous animal studies showed a promising future for this peptide as it not only promotes GH secretion, but does so by maintaining a regular circadian rhythm and normal physiological response.

CJC-1295 also presented itself with only moderate side effects and showed, like many other peptides, modest oral and superb subcutaneous bioavailability in mice testing.

 

References:

Ionescu and L. A. Frohman, “Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog,” J. Clin. Endocrinol. Metab., vol. 91, no. 12, pp. 4792–4797, Dec. 2006.

Jetté, Lucie & Leger, Roger & Thibaudeau, Karen & Benquet, Corinne & Robitaille, Martin & Pellerin, Isabelle & Paradis, Véronique & Wyk, Pieter & Pham, Khan & Bridon, Dominique. (2005). hGRF1-29-Albumin Bioconjugates Activate the GRF Receptor on the Anterior Pituitary in Rats: Identification of CJC-1295 as a Long Lasting GRF Analog.

Alba et al., “Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse,” Am. J. Physiol. Endocrinol. Metab., vol. 291, no. 6, pp. E1290-1294, Dec. 2006.

Volpe, G. Coukos, A. Barreca, G. Giordano, P. G. Artini, and A. R. Genazzani, “Clinical use of growth hormone-releasing factor for induction of superovulation,” Hum. Reprod., vol. 6, no. 9, pp. 1228–1232, Oct. 1991.

Reviews

There are no reviews yet.

Write a review

Your email address will not be published. Required fields are marked *

42 + = 47

Bestsellers

AICAR 50mg

$55.00
(0 Reviews)
AICAR (5-Aminoimidazole-4-carboxamide ribonucleoside) is one of the most commonly used pharmacological modulators of AMPK activity. AMPK is an enzyme that acts as a fuel gauge in high energy consumption situations. Of course, AICAR can also be synthesized in the lab, which is why it continues to be studied due to its potential in performance boost.

Tesamorelin

$70.00$125.00
(0 Reviews)
Tesamorelin is a synthetic growth hormone-releasing hormone (GHRH) analog. It was based on the 44 amino acids sequence of GHRH and contains a trans-3 hexenoic group to protect it from enzymatic degradation. These modifications allow it to be more stable and have a longer half-life.   Just like Sermorelin, Ipamorelin or GHRP-2, Tesamorelin is considered a growth hormone secretagogue (GHS) which stimulates the secretion of GH and increases the level of insulin-like growth factor (IGF-1). The importance of IGF-1 is it tends to be lower in patients with obesity, diabetes and especially in those with lipodystrophy. References: 
  1. Sinha DK, Balasubramanian A, Tatem AJ, Rivera-Mirabal J, Yu J, Kovac J, Pastuszak AW, Lipshultz LI. Beyond the androgen receptor: the role of growth hormone secretagogues in the modern management of body composition in hypogonadal males. Transl Androl Urol. 2020 Mar;9(Suppl 2):S149-S159. doi: 10.21037/tau.2019.11.30. PMID: 32257855; PMCID: PMC7108996.

GHRP 2 10mg

$50.00
(0 Reviews)
GHRP-2, also known as pralmorelin, is a synthetic growth hormone secretagogue, which specifically targets ghrelin (growth hormone receptor). The significance of targeting ghrelin becomes apparent when we see what are its two main effects – growth hormone secretion and meal initiation.   GHRP-2 was a pioneering growth hormone (GH) secretagogue and is currently used to evaluate GH deficiency and secondary adrenal failure.

Semaglutide

$105.00$190.00
(0 Reviews)
This is a synthetic peptide modeled after the naturally occurring hormone glucagon-like peptide-1 (GLP-1). GLP-1 is an incretin, a gut-derived peptide secreted in response to a meal, that regulates insulin secretion based on glucose levels in the blood. This GLP-1 agonist was developed specifically to have an extended half-life without losing potency. Since it falls under the category of glucagon-like peptide-1 receptor agonists, it acts to prompt the body to secrete more insulin and inhibit glucagon secretion. By allowing the body to secrete more insulin and inhibiting the secretion of glucagon, this joint effort brings blood glucose levels down.

KPV 10mg

$100.00
(0 Reviews)
KPV is one of several short peptide derivatives of alpha-melanocyte stimulating hormones, which originates from the C-terminal fragment of alpha-MSH.   Due to Lysine-proline-valine’s (KPV’s) potency, this peptide has been garnering more and more attention from the scientific community, and we are eager to see what the future lab research is going to show.

Melanotan 2 10mg

$55.00
(0 Reviews)
Melanotan 2 (MT-2) is a synthetic analogue of alpha-melanocyte-stimulating hormone, created in the 1980s. It has been found to act as a non-selective agonist of melanocortin receptors MC1, MC3, MC4 and MC5. It has been clinically documented that melanotan II activates MC1 receptor, which leads to melanogenesis, which is why this particular peptide was deemed “barbie drug.” References:
  1. https://pubmed.ncbi.nlm.nih.gov/8637402/
  2. https://www.sciencedirect.com/science/article/abs/pii/S0022354915495474
  3. https://www.sciencedirect.com/science/article/abs/pii/S2211266915000055

Thymosin Alpha 1 10mg

$120.00
(0 Reviews)
When speaking about thymosin alpha 1, we know that it’s a 28 amino acid peptide which naturally occurs in the thymus gland and has been known to modify and regulate the immune system via its action as a toll-like receptor and TLR-2 agonist.   Naturally present thymosin 1 in the body intensifies t-cell maturation and differentiation, the activity of natural killer cells, and also cytokine-mediated inflammation.
Back to Top
Product has been added to your cart