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CJC-1295 + Ipamorelin Blend

CJC-1295 + Ipamorelin Blend

Research Peptide | Lyophilized Powder | Batch Tested

Tested for
Purity
Size
$125.00
$1.25/mg
In StockLatest batch: CP10-260601
1

For laboratory research use only. Not for human or animal consumption. Insulated shipping · Styrofoam box available.

Product Overview

This blend combines the GHRH analog CJC-1295 (No DAC) with the selective secretagogue Ipamorelin — one of the most classic pairings in growth-hormone-axis research, because the two act on different receptors.

Batch CP10-260601Tested Jun 1, 2026
TestResultStatus
Purity98.6%Passed ✓
Batch CP20-260601Tested Jun 1, 2026
TestResultStatus
Purity98.9%Passed ✓
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Research Information

The combination is used to study synergistic growth-hormone release: GHRH-receptor stimulation (CJC-1295) and ghrelin-receptor activation (Ipamorelin) together produce a stronger, more physiological GH pulse than either alone, a widely used model for probing GH-secretion mechanisms. Supplied strictly for in-vitro and laboratory research use only — not for human or animal consumption.

CJC-1295 + Ipamorelin Blend Research & Studies

What is CJC-1295 + Ipamorelin Blend?

CJC-1295 + Ipamorelin Blend is a research peptide combination pairing the GHRH analog CJC-1295 (No DAC) with the selective growth-hormone secretagogue Ipamorelin. Laboratory investigators use this pairing to examine coordinated stimulation of the growth-hormone axis through two distinct receptor systems. The blend is supplied exclusively for in-vitro and controlled laboratory research applications. It is not intended for any form of consumption or administration outside experimental model systems.

Mechanism of Action

CJC-1295 (No DAC) binds GHRH receptors on somatotroph cells, activating adenylate cyclase and elevating intracellular cAMP to promote growth-hormone gene transcription and release. Ipamorelin selectively engages the ghrelin receptor GHS-R1a, triggering calcium-dependent signaling that further amplifies GH secretion. When studied together, the dual-receptor input produces a coordinated pulse that more closely models endogenous GH release patterns than either ligand alone. This complementary mechanism is the primary rationale for their combined use in mechanistic research.

Primary Areas of Research

Investigators employ the blend to probe synergistic growth-hormone release dynamics in pituitary cell cultures and isolated tissue preparations. Studies focus on receptor crosstalk between GHRH-R and GHS-R1a pathways, pulse amplitude modulation, and feedback interactions involving somatostatin. The combination also serves as a tool for examining second-messenger integration and the temporal characteristics of physiological GH secretory episodes under controlled laboratory conditions.

Key Research Findings

Experimental models consistently demonstrate that concurrent GHRH-receptor and ghrelin-receptor activation yields greater GH output than either stimulus applied separately. This synergy is attributed to complementary intracellular signaling cascades that converge on the secretory machinery of somatotrophs. Research using the blend has helped clarify how dual-pathway stimulation can generate more robust, physiologically patterned GH pulses. Such findings inform broader understanding of hypothalamic-pituitary regulation without implying any applied use outside the laboratory.

Research Handling & Considerations

The blend is intended solely for in-vitro assays and laboratory model systems. Researchers typically reconstitute lyophilized material in appropriate sterile solvents under aseptic conditions and store aliquots according to standard peptide-stability protocols. Experimental design should account for the short half-life of CJC-1295 (No DAC) relative to DAC-containing analogs and the high receptor selectivity of Ipamorelin. All work must remain confined to controlled research environments.

Frequently Asked Questions

CJC-1295 (No DAC) acts at the GHRH receptor while Ipamorelin selectively activates the ghrelin receptor GHS-R1a, allowing investigators to study dual-pathway stimulation of somatotroph cells.

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