Ultima-CJC1295 DAC 2mg-int

$22.46

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

SKU: ULTIMA-AAS-7597 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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SKUULTIMA-AAS-7597EURO48542EURO67717EURO63953EURO31677EURO69147
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DescriptionACTIVE HALF-LIFE ?CLASSIFICATION ?DOSAGE ?ACNE ?WATER RETENTION ?HBR ?HEPATOTOXICITY ?AROMATIZATIONACTIVE HALF-LIFE 7-9 days  CLASSIFICATION Anabolic Steroid  DOSAGE 400-1200 mg/week  ACNE Yes  WATER RETENTION Yes  HBR Perhaps  HEPATOTOXICITY No  AROMATIZATION YesACTIVE HALF-LIFE 7-9 days  CLASSIFICATION Anabolic Steroid  DOSAGE 400-1200 mg/week  ACNE Yes  WATER RETENTION Yes  HBR Perhaps  HEPATOTOXICITY No  AROMATIZATION YesACTIVE HALF-LIFE Several Minutes  CLASSIFICATION Peptide Hormone  DOSAGE 500 mcg/day  ACNE No  WATER RETENTION No  HBR No  HEPATOTOXICITY No  AROMATIZATION NoACTIVE HALF-LIFE 1.5 hours  CLASSIFICATION Peptide Hormone  DOSAGE 25-50 mcg/day  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 No
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.During any physical work the body produces insulin-like growth factor. It leads to the appearance of a large number of muscle cells causing muscle growth. In addition this substance helps to accelerate the healing process. One of the types of this hormone is a peptide Peg MGF. It is similar to growth hormone because of its characteristics but the main difference is that it does not affect the ligaments and cartilage condition. An active substance MGF has a very short half-life. To increase the effectiveness of the hormone it is possible to create a kind of capsule consisting of polyethylene glycol surrounding the hormone. The human’s body does not react to polyethylene glycol and the transit time of the hormone in the organism can be increased. With this solution Peg MGF peptide has a long lasting effect allowing you to achieve your goals. Peg MGF feedbacks show that this peptide is especially popular among young athletes. It has been proved that the peptide has less effect on elder people so it depends on the age of the athlete. Researches show that the full course allows to increase muscle size by 15%. The effects of Peg MGF It is recommended to buy Peg MGF when you need to: increase the growth of muscle tissue; reduce the number of fat cells in the body; increase endurance and strength; achieve an apparent muscle relief; accelerate the recovery of muscle cells after workout or injury; achieve detailed venous pattern; stimulate the formation of new venous branches. In the addition to the above points, Peg MGF improves immune forces of the body, lowers cholesterol level in blood, strengthens the nervous system, stimulates the formation of bone marrow cells, improves skin and prevents the negative impact of the increased heart stress. Application and dosage of Peg MGF The peptide can be administered in two ways. In first case the dosage for Peg MGF is from 100 to 200 mcg. Preparation can be administered every 2-3 days during 5 or 6 weeks. Then the pause for 3 weeks must be made. It is recommended to inject the peptide immediately after workouts. The course is repeated if necessary until the desired result is achieved. Side effects and contraindications Before beginning a hormone course you must carefully read the instructions for the use of Peg MGF. In rare cases there are possible some complications such as increased growth and size of limbs and prostatic hyperplasia. So peptide administration is allowed under the careful attention of experienced professionals and after consulting a doctor.GHRP-6 peptide which is structurally very similar to its predecessor, GHRP-2 The main difference is that the GHRP-6 increases appetite in some people. Both peptides can be used together to achieve better synergistic effects. Studies have shown that the highest concentrations of growth hormone in the blood is achieved just combinations of GHRP-6 and GHRP-2. GHRP-6 stimulates the pituitary gland to produce GH. GHRP can be effectively used in the treatment of growth hormone deficiency. GHRP-6 is highly effective in increasing blood levels of the hormone HGH and IGF-1. GHRP-6 stimulates and strengthens the immune system, has a strong anabolic – for massive muscle gains and strength, helps burn body fat, has a very strong anti-aging effect, smooths wrinkles, improves the condition of hair and skin, gives a very good sleep and excellent regeneration, increases bone strength, has anti-inflammatory effects, brings a sense of the large influx of energy and vitality, and causing general overall rejuvenation of the body and all of its body tissues. GHRP-6 helps very effectively to gain muscle mass, increase strength, recovery and burn fat. GHRP-6 improves energy metabolism. Combining GHRP 6 with CJC 1295 The combined use of CJC 1295 peptide without DAC can greatly enhance its results in conjunction with GHRP 6. Combining GHRP 6 with T3 The efficiency of GHRP 6 can greatly amplify with little high levels of T3 in the body.Tesamorelin (Tesamorelin) is made with growth hormone-releasing factor (GRF). Tesamorelin is used to reduce excess fat around the stomach that is caused by taking certain HIV medications. This condition is also called lipodystrophy (LYE-poe-DIS-troe-fee). Tesamorelin is not a weight-loss medication and should not be used to treat obesity. Tesamorelin (Tesamorelin for injection) is indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Limitations of Use: Since the long-term cardiovascular safety and potential long-term cardiovascular benefit of Tesamorelin treatment have not been studied and are not known, careful consideration should be given whether to continue Tesamorelin treatment in patients who do not show a clear efficacy response as judged by the degree of reduction in visceral adipose tissue measured by waist circumference or CT scan. Tesamorelin is not indicated for weight loss management (weight neutral effect). There are no data to support improved compliance with anti-retroviral therapies in HIV-positive patients taking Tesamorelin. General Dosing Information The recommended dose of Tesamorelin is 2 mg injected subcutaneously once a day. The recommended injection site is the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel. Reconstitution Procedure Tesamorelin must be reconstituted with the diluent provided with the product. Reconstitute the 2 mg vial of Tesamorelin with 2.1 mL of diluent. Mix by rolling the vial gently in your hands for 30 seconds. Do not shake. Detailed instructions for reconstituting Tesamorelin are provided in the INSTRUCTIONS FOR USE leaflet enclosed in the boxes containing Tesamorelin and diluent. Administer Tesamorelin immediately following reconstitution and throw away any unused Tesamorelin solution. If not used immediately, the reconstituted Tesamorelin solution should be discarded. Do not freeze or refrigerate the reconstituted Tesamorelin solution. Administration Reconstituted Tesamorelin solution should always be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Tesamorelin must be injected only if the solution is clear, colorless and without particulate matter. Tesamorelin should be injected subcutaneously into the skin on the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel.
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