Ultima-CJC1295 no DAC 2mg-int

$18.19

Availability: In Stock

ACTIVE HALF-LIFE
?CLASSIFICATION
?DOSAGE
?ACNE
?WATER RETENTION
?HBR
?HEPATOTOXICITY
?AROMATIZATION

SKU: ULTIMA-AAS-2744 Categories: , , ,

Description

Products are shipping without brand label for security reasons.

CJC-1295 is a synthetic GHRH (growth hormone releasing hormone) analogue made up of 30 amino acids. It has been found to be highly effective with regards to the increase of growth hormone secretion and IGF-1 without negatively affecting the pulsatility of GH secretion.

CJC-1295 is often combined with Ipamorelin due to its enhanced specificity as a GHRH. This peptide generates similar increases in growth hormone secretion, but without the appetite stimulation and increase in cortisol, acetylcholine, prolactin, and aldosterone seen with other peptides in its class. This peptide has been found to be very well-tolerated and perfect when combined with Ipamorelin.

Gland Stimulated: Pituitary

Benefits of CJC-1295:

Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin
Increased Body Weight and Length through increased protein synthesis
Increased Muscle Growth
Increased Bone Density
Improved Immune Function
Improved Cognition and Memory
Increased Collagen Production
Increased Fat Loss
Increased Cellular Repair and Regeneration

CJC-1295 also promotes slow wave deep sleep, which is responsible for the highest level of muscle growth and memory retention and rejuvenation

Two types of CJC 1295:

GHRH (growth hormone releasing hormone) is produced in the hypothalamus. Its pulsatile release from the hypothalamus triggers a pulsatile release of GH from the pituitary gland. GHRH has a very short half-life of only a few minutes (half-life = the time required to remove half of the substance from the blood. The shorter the half-life, the more rapidly the substance is removed from the body, and the less its effect on the body).

The first 29 amino acids of GHRH is the active segment. They are available as a manufactured peptide called Sermorelin. Sermorelin was further modified to increase its half-life to 30 minutes. This is called CJC 1295. CJC-1295 was further modified by adding DAC (Drug Affinity Complex) to it. DAC binds to a blood protein called albumin, which increases it’s half-life to 8 days. It is called CJC 1295 + DAC. CJC 1295 can also be compounded in a non-DAC form which mimics a more normal physiologic GH spike each night.

The longer half-life from the DAC binding to albumin means injections are only required once or twice per week. However, the long half-life and relatively constant blood level provide a constant stimulus for GH release from the pituitary through the GHRH receptor, which is not physiological. This can decrease the GH pulse amplitude which will result in decreased GH tissue stimulation.

Safety:

It is recommended when using a long-acting CJC molecule to have ‘hormone holidays’ of three months each three to six months, to allow the pituitary to ‘recover’. During the holidays, Sermorelin is used instead of CJC 1295 + DAC.

The ‘hormone holidays’ may also minimize the risk of GH resistance developing. This resistance, or insensitivity, may occur via antibodies forming that bind to and inactivate GH, or by a decreased number of GH receptors on tissues (down-regulation). These are theoretical concerns as no long-term studies have been undertaken to clarify the issues.
Side effects of CJC-1295 may include injection site reactions (irritation, erythema, induration, pain, itching), headache, diarrhea, vasodilation (flushing, warmth, transient hypotension), nausea, abdominal pain.

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SettingsUltima-CJC1295 no DAC 2mg-int removeCJC-1295 NO-DAC removePAL-GHK 10mg Gold removeIGF 1-LR3 1mg Gold removeCJC-1295 2mg Gold removeTest 400 Gold remove
NameUltima-CJC1295 no DAC 2mg-int removeCJC-1295 NO-DAC removePAL-GHK 10mg Gold removeIGF 1-LR3 1mg Gold removeCJC-1295 2mg Gold removeTest 400 Gold remove
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SKUULTIMA-AAS-2744RF-Axiom peptides-domestic6594EURO25999EURO87915EURO73688EURO48542
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DescriptionACTIVE HALF-LIFE ?CLASSIFICATION ?DOSAGE ?ACNE ?WATER RETENTION ?HBR ?HEPATOTOXICITY ?AROMATIZATIONACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE  CLASSIFICATION Peptide Hormone  DOSAGE  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE 7-9 days  CLASSIFICATION Anabolic Steroid  DOSAGE 400-1200 mg/week  ACNE Yes  WATER RETENTION Yes  HBR Perhaps  HEPATOTOXICITY No  AROMATIZATION Yes
ContentProducts are shipping without brand label for security reasons. CJC-1295 is a synthetic GHRH (growth hormone releasing hormone) analogue made up of 30 amino acids. It has been found to be highly effective with regards to the increase of growth hormone secretion and IGF-1 without negatively affecting the pulsatility of GH secretion. CJC-1295 is often combined with Ipamorelin due to its enhanced specificity as a GHRH. This peptide generates similar increases in growth hormone secretion, but without the appetite stimulation and increase in cortisol, acetylcholine, prolactin, and aldosterone seen with other peptides in its class. This peptide has been found to be very well-tolerated and perfect when combined with Ipamorelin. Gland Stimulated: Pituitary Benefits of CJC-1295: Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin Increased Body Weight and Length through increased protein synthesis Increased Muscle Growth Increased Bone Density Improved Immune Function Improved Cognition and Memory Increased Collagen Production Increased Fat Loss Increased Cellular Repair and Regeneration CJC-1295 also promotes slow wave deep sleep, which is responsible for the highest level of muscle growth and memory retention and rejuvenation Two types of CJC 1295: GHRH (growth hormone releasing hormone) is produced in the hypothalamus. Its pulsatile release from the hypothalamus triggers a pulsatile release of GH from the pituitary gland. GHRH has a very short half-life of only a few minutes (half-life = the time required to remove half of the substance from the blood. The shorter the half-life, the more rapidly the substance is removed from the body, and the less its effect on the body). The first 29 amino acids of GHRH is the active segment. They are available as a manufactured peptide called Sermorelin. Sermorelin was further modified to increase its half-life to 30 minutes. This is called CJC 1295. CJC-1295 was further modified by adding DAC (Drug Affinity Complex) to it. DAC binds to a blood protein called albumin, which increases it's half-life to 8 days. It is called CJC 1295 + DAC. CJC 1295 can also be compounded in a non-DAC form which mimics a more normal physiologic GH spike each night. The longer half-life from the DAC binding to albumin means injections are only required once or twice per week. However, the long half-life and relatively constant blood level provide a constant stimulus for GH release from the pituitary through the GHRH receptor, which is not physiological. This can decrease the GH pulse amplitude which will result in decreased GH tissue stimulation. Safety: It is recommended when using a long-acting CJC molecule to have 'hormone holidays' of three months each three to six months, to allow the pituitary to 'recover'. During the holidays, Sermorelin is used instead of CJC 1295 + DAC. The 'hormone holidays' may also minimize the risk of GH resistance developing. This resistance, or insensitivity, may occur via antibodies forming that bind to and inactivate GH, or by a decreased number of GH receptors on tissues (down-regulation). These are theoretical concerns as no long-term studies have been undertaken to clarify the issues. Side effects of CJC-1295 may include injection site reactions (irritation, erythema, induration, pain, itching), headache, diarrhea, vasodilation (flushing, warmth, transient hypotension), nausea, abdominal pain.This peptide CJC-1295 NO-DAC imitates the function of GHRF or Growth Hormone Releasing Factors by which it increases and enhances the release of Growth Hormones in the Body. Use this from 1mg-2mg for 5 days out of 7 days from 6pm-8pm for best results.Insulin-like growth factor-1 (IGF-1) helps encourage normal bone and tissue growth and development and also has the ability to decrease blood glucose levels. IGF-1 advances to fat cells and therefore burns fat. Subsequently, it increases lean body mass and decreases fat. These effects are desired mostly by athletes and bodybuilders. Increased IGF-1 levels are also comparable to weight gain. This weight gain is a result of lean body mass growth, not fat production. IGF-1 is favored in the bodybuilding industry and for people who workout regularly. It helps enhance recovery time after workout and improves energy during the workout. IGF-1 injections are common for adults and children if they have a growth hormone deficiency. IGF-1 contains many necessary amino acids that can help children who are not developing at a standard rate and supplement adults that are deficient. Research has also shown that the anabolic effects of IGF-1 may reflect inhibited protein breakdown and stimulated protein synthesis in skeletal muscle and that this response may be caused by a direct effect of IGF-1 on muscle tissue, therefore assisting burns on the skin and other tissue abnormalities. Mechanism of Action IGF-1 is a hormone found naturally in human blood. Its primary function is to manage the effects of growth hormone in the body. Normal IGF-1 and growth hormone functions include tissue and bone growth. IGF-1 is formed in different tissues as a result of growth hormone in the blood. IGF-1 promotes systemic body growth, and has growth-stimulating effects on mostly every cell in the body, mainly bone, cartilage, skeletal muscle, liver, kidney, nerve, skin and lung cells. As well as the insulin-like effects, IGF-1 can also manage cellular DNA synthesis. Administration Mode of Administration: Subcutaneous injection to a fleshy part of the body, typically to the stomach or abdominal area. IGF-1 can also be administered intramuscularly. Before administering IGF-1, always be sure to use a clean and sterile syringe. Hold the IGF-1 vial upright and insert the syringe in the center of the cap. Draw the plunger until you have the correct amount (see ‘Dosage’ below) in the syringe and carefully remove it. Before administering the syringe, use alcohol to cleanse the area of skin. Pinch the skin around the area to be injected, leave about 2 cm on each side. Hold the syringe at a 90 degree angle to your skin and swiftly insert the syringe. Depress the plunger fully, until the syringe is empty, and carefully draw out. Dosage Dosage Amount: For lean muscle growth and fat loss 40 mcg - 50 mcg daily (men) 10 mcg - 20 mcg daily (women) IGF-1 should not be injected more than twice daily A typical dosage cycle of IGF-1 will continue for 2 to 12 weeks Children and adults who are prescribed IGF-1 for development deficiency should consult with a care provider about correct dosing. Side Effects The side effects of IGF-1 can be similar to those of other growth hormones. These include growth of excess body tissue, also known as acromegaly, and damage to the joints, liver, and heart. IGF-1 could possibly cause joint pain, muscle pain, headaches and nausea. IGF-1 can also decrease levels of blood glucose, resulting in hypoglycemia. Researchers also associate IGF-1 with an increased risk of developing some cancers, such as lung, breast, colorectal and prostate. Benefits Facilitation of protein synthesis in the body Regulation of stored fat and channeling it to be used for energy production, resulting in fat loss Promotion of positive effects on metabolism and increasing lean body mass and muscle growth Protection against autoimmune disease, heart disease and plaque buildup Aid development in young children and adults deficient in essential amino acids Improvement in blood sugar regulation Promotion of optimal health, wellness and fitness in usersCJC-1295 is a synthetic GHRH (growth hormone releasing hormone) analogue made up of 30 amino acids. It has been found to be highly effective with regards to the increase of growth hormone secretion and IGF-1 without negatively affecting the pulsatility of GH secretion. CJC-1295 is often combined with Ipamorelin due to its enhanced specificity as a GHRH. This peptide generates similar increases in growth hormone secretion, but without the appetite stimulation and increase in cortisol, acetylcholine, prolactin, and aldosterone seen with other peptides in its class. This peptide has been found to be very well-tolerated and perfect when combined with Ipamorelin. Gland Stimulated: Pituitary Benefits of CJC-1295: Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin Increased Body Weight and Length through increased protein synthesis Increased Muscle Growth Increased Bone Density Improved Immune Function Improved Cognition and Memory Increased Collagen Production Increased Fat Loss Increased Cellular Repair and Regeneration CJC-1295 also promotes slow wave deep sleep, which is responsible for the highest level of muscle growth and memory retention and rejuvenation Two types of CJC 1295: GHRH (growth hormone releasing hormone) is produced in the hypothalamus. Its pulsatile release from the hypothalamus triggers a pulsatile release of GH from the pituitary gland. GHRH has a very short half-life of only a few minutes (half-life = the time required to remove half of the substance from the blood. The shorter the half-life, the more rapidly the substance is removed from the body, and the less its effect on the body). The first 29 amino acids of GHRH is the active segment. They are available as a manufactured peptide called Sermorelin. Sermorelin was further modified to increase its half-life to 30 minutes. This is called CJC 1295. CJC-1295 was further modified by adding DAC (Drug Affinity Complex) to it. DAC binds to a blood protein called albumin, which increases it's half-life to 8 days. It is called CJC 1295 + DAC. CJC 1295 can also be compounded in a non-DAC form which mimics a more normal physiologic GH spike each night. The longer half-life from the DAC binding to albumin means injections are only required once or twice per week. However, the long half-life and relatively constant blood level provide a constant stimulus for GH release from the pituitary through the GHRH receptor, which is not physiological. This can decrease the GH pulse amplitude which will result in decreased GH tissue stimulation. Safety: It is recommended when using a long-acting CJC molecule to have 'hormone holidays' of three months each three to six months, to allow the pituitary to 'recover'. During the holidays, Sermorelin is used instead of CJC 1295 + DAC. The 'hormone holidays' may also minimize the risk of GH resistance developing. This resistance, or insensitivity, may occur via antibodies forming that bind to and inactivate GH, or by a decreased number of GH receptors on tissues (down-regulation). These are theoretical concerns as no long-term studies have been undertaken to clarify the issues. Side effects of CJC-1295 may include injection site reactions (irritation, erythema, induration, pain, itching), headache, diarrhea, vasodilation (flushing, warmth, transient hypotension), nausea, abdominal pain.
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Additional information
PEPDITES

2mg, 5mg