IGF-1 LR3

Long R3 IGF-I · 83-residue IGF-I analogue for cell-culture and receptor research

≥ 99.0% · target, verify batch COACAS 143045-27-6RUO
Batch COA
MOQ1 kit (10 vials) per SKU
Supplied form83-residue engineered, three-disulfide IGF-I protein analogue
Lead time14–21 days
IGF-1 LR3 — Lyophilized material; confirm released-lot appearance on the COA
IGF-1 LR3 — Lyophilized material; confirm released-lot appearance on the COA · Representative packaging image · verify the ordered lot
Representative packaging image · verify the ordered lot

Decision summary

Key benefits

  • Research value: IGF-1 LR3 supports controlled studies of IGF1R signaling, IGFBP resistance, mitogenic/anti-apoptotic pathways, cell-line growth and bioprocess optimization
  • Animal anabolic, organ-growth and metabolic results do not establish human muscle growth, fat loss, recovery, tissue repair or anti-aging benefits.
Published research context is presented for literature orientation only. It is not a dosing, treatment or human-use instruction.

Qualification data

Specifications to confirm against the released lot

CAS
143045-27-6
Formula
C400H619N111O115S9 (three disulfides; reduced chain C400H625N111O115S9)
Molecular weight
9111.45 g/mol
Appearance
Lyophilized material; confirm released-lot appearance on the COA
Purity
≥ 99.0% · target, verify batch COA
Storage
Use the released-lot COA and stability statement for the supplied recombinant form. Define temperature, container closure, freeze-thaw allowance, adsorption controls, solvent, concentration and microbiological limits. Repligen instructions apply to its own qualified cell-culture formulations and are not automatically transferable to another lot.
MOQ
1 kit (10 vials) per SKU
Lead time
14–21 days

Qualification matrix

Identity, purity and content are separate release questions.

Identity

Confirm the stated molecule and supplied form. Start with the matching batch COA; request sequence-level evidence only when the buyer's written procedure requires it and availability or a separate scope has been agreed.

Purity

Review RP-HPLC method conditions, wavelength, integration and related-peak handling. A percentage without the method is not enough.

Content

Net peptide content is not the same as gross lyophilized powder weight. Ask which assay supports the stated amount and whether water/counter-ion is addressed.

Stability

Follow the storage condition stated on the batch COA or label from receipt onward.

Research context

What researchers study about IGF-1 LR3

IGF-1 LR3 (Long R3 IGF-I) is an 83-residue recombinant analogue of human IGF-I, engineered with a 13-residue N-terminal extension and an Arg substitution at position 3 to reduce binding to IGF-binding proteins. Its established commercial role is as a mammalian cell-culture supplement and research reagent. Direct evidence is predominantly in vitro and animal research; no qualifying interventional human trial of LR3 IGF-I was identified. FDA GSRS records the substance identity but explicitly states that UNII availability does not imply regulatory review or approval. This catalog material is RUO and not a finished dosage form.

  • Evidence contexts include recombinant cell-culture supplementation, IGF1R/IGFBP mechanism research, and animal studies of growth, endocrine feedback and tissue biology
  • Native IGF-I studies, epidemiology, veterinary case series and other analogues are indirect context and cannot establish LR3 human efficacy or safety.

Mechanism context

The question the literature is testing

IGF-1 LR3 activates the type 1 IGF receptor. Its N-terminal extension and Arg3 substitution markedly reduce affinity for IGF-binding proteins, increasing receptor availability in relevant in vitro systems. Downstream signaling can include PI3K/Akt/mTOR and MAPK/ERK pathways, but pathway activation does not establish a clinical outcome or lot-specific biological potency without a qualified assay.

Evidence map

Research routes and exposure context

Evidence tierAnalytical / laboratory context
Routes reported in sources
No administration route applies
Dose / exposure contextProtocol-specific; verify the cited primary source
Routes and exposure contexts summarize cited studies or approved finished-product labels. They are not instructions for administering this RUO material; no customer dose is provided.

Evidence boundaries

Compatibility, limitations and decision context

  • IGF-1 LR3 has no established administered-human safety profile
  • Mitogenic and glucose-regulatory activity creates material experimental hazards, and animal findings show strong species and protocol dependence
  • WADA prohibits IGF-1 and its analogues for athletes subject to the Code
  • Handle as an RUO recombinant growth factor under institutional risk controls; this record provides no injection, hypoglycaemia-management, cancer-screening or athletic-use advice.

Interactions reported in the literature

  • No human combination-use guidance is provided
  • Cell-culture co-supplementation with insulin is a process-development question requiring cell-line-specific titration and controls; it is not evidence for co-administration
  • Vendor stacking claims involving HGH, insulin, secretagogues, anabolic agents or other peptides are excluded.
Literature context is not a supplier release result or human-use instruction. Follow your institution's approved laboratory risk assessment.

Batch documentation

IGF-1 LR3 batch COAs

Laboratory: Manufacturer's QC laboratoryTests: HPLC purity · MS identity · endotoxin · fill amount

  • Blurred preview of a IGF-1 LR3 100 mcg batch COA100 mcg
  • Blurred preview of a IGF-1 LR3 1000 mcg batch COA1000 mcg

Previews are blurred on purpose so the documents cannot be reused; third-party reports show their first page only. Sales sends the clear full version for the product and strength you ask about.

Independent test fails? Full refund.

Representative records, refreshed periodically

Published COAs show recent representative batches and may not be the newest. For a quote or shipment, sales confirms the lot and sends its COA.

Third-party reports, added progressively

Previews of the first page of third-party reports are on our Quality page and on the matching product pages; sales sends the full report on request. You can also send any vial from your order to an independent laboratory of your choice. Unless agreed otherwise in writing, the buyer pays for optional testing.

Help reviewing your COA

Need help reading a batch COA or third-party report? Sales can explain the test items, specifications and how the results relate to the lot under discussion.

On every batch COA: HPLC purity · MS identity · endotoxin · fill amount · Verify LyoPep

Ask for the current packet, not a generic certificate

  • Require the complete 83-residue sequence, correct disulfide connectivity, high-resolution intact and reduced mass, orthogonal identity, protein-content assay, aggregate and fragment profile, residual host-cell proteins/DNA where relevant, endotoxin or bioburden limits appropriate to the model, water and residual process impurities
  • HPLC area purity or intact mass alone does not establish correct folding or biological activity.
Batch COA for the released lotHPLC purity with method contextMS identity resultEndotoxin resultFill amount (measured content per vial)SDS and handling statement

Available fills

Quote the fill and pack configuration you need

Reference SKUFillBase pack
IGF101100 mcg10 vials
IGF11000 mcg10 vials
IGF22 mg10 vials

Other format

Also available as a nasal spray (US stock)

Black 10 mL nasal spray bottle with a clear cap
10 mL nasal spray bottle

Besides lyophilized vials, IGF-1 LR3 is also supplied as a nasal spray solution, shipped from our US stock.

Strengths
0.1 mg · 1 mg
Bottle sizes
10 mL or 20 mL
Minimum order
10 bottles per strength and bottle size
Ships from
Our US stock

Handling

Plan storage before the parcel arrives

Use the released-lot COA and stability statement for the supplied recombinant form. Define temperature, container closure, freeze-thaw allowance, adsorption controls, solvent, concentration and microbiological limits. Repligen instructions apply to its own qualified cell-culture formulations and are not automatically transferable to another lot.

State the destination and timing so receipt can be planned, then move the material into its stated storage condition on arrival.

Buyer FAQ

Terms to settle before the purchase order

Can a buyer arrange third-party testing?+

Yes. You can send any vial from your order to an independent laboratory of your choice. If you want the laboratory, specification, sampling, method and acceptance rule agreed with us before testing, sales confirms them in writing. Unless otherwise agreed in writing, the buyer pays the cost of this optional testing.

What if my own lab test shows the product is out of specification?+

Send any vial from your order to an independent laboratory of your choice. If the report shows the product does not meet the specification on its COA — purity below the stated minimum, or an identity that does not match — share the report with our sales team and we refund that product in full.

Does HPLC purity prove peptide content?+

No. Chromatographic purity describes the relative peak profile under a stated method. Identity, water, counter-ion, residual solvents and assay/content may require separate methods.

How should material be stored after delivery?+

Move it into the storage condition stated on the batch COA or label as soon as it arrives, and record the package condition on receipt.

How are payment terms handled?+

Available methods and milestones depend on order value, destination and project type. The pro forma invoice should state currency, bank details, fees, payment milestones and the release condition.

Why must the testing laboratory understand peptide chemistry?+

Free-base and salt forms, hydrophilic and hydrophobic sequences, aggregation and adsorption can change sample preparation and method suitability. Use a laboratory experienced with the molecule class.

These are buyer-qualification references, not claims that this RUO material is regulated, certified or released under those frameworks. Applicability depends on the buyer's workflow and jurisdiction.

Selected sources

Literature behind the research context

  • Key sources: FDA GSRS UNII M9L22Y19H9; Repligen LONG R3 IGF-I product and FAQ/quality documents; WADA 2026 Prohibited List; Tomas et al. 1992 (PMID 1378742); the 1995 guinea-pig study (PMID 7561636); the 1999 satellite-cell study (PMID 10632630); and the listed IGF-1 signaling, anti-doping and tendon reviews. Evidence is labelled as direct LR3, parent-pathway, animal, veterinary or secondary context.
  1. 01

    Novel recombinant fusion protein analogues of insulin-like growth factor (IGF)-I indicate the relative importance of IGF-binding protein and receptor binding for enhanced biological potency

    Journal of Molecular Endocrinology · 1992 · peer-reviewed original research

    Open source
  2. 02

    Long R3 insulin-like growth factor-I (IGF-I) infusion stimulates organ growth but reduces plasma IGF-I, IGF-II and IGF binding protein concentrations in the guinea pig

    Journal of Endocrinology · 1995 · peer-reviewed original research (animal study)

    Open source
  3. 03

    Contribution of satellite cells to IGF-I induced hypertrophy of skeletal muscle

    Acta Physiologica Scandinavica · 1999 · peer-reviewed original research (animal study)

    Open source
  4. 04

    Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy

    Cells · 2020 · peer-reviewed review

    Open source
  5. 05

    Insulin-Like Growth Factor-1 (IGF-1) and Its Monitoring in Medical Diagnostic and in Sports

    Biomolecules · 2021 · peer-reviewed review

    Open source
  6. 06

    Doping and sports endocrinology: growth hormone, IGF-1, insulin, and erythropoietin

    Revista Clínica Española (Barcelona) · 2023 · peer-reviewed review

    Open source
  7. 07

    Insulin-like growth factor-1 (IGF-1) empowering tendon regenerative therapies

    Frontiers in Bioengineering and Biotechnology · 2025 · peer-reviewed review

    Open source
  8. 08

    Intralesional injection of insulin-like growth factor-I for treatment of superficial digital flexor tendonitis in Thoroughbred racehorses: 40 cases (2000-2004)

    Journal of the American Veterinary Medical Association · 2011 · peer-reviewed original research (veterinary clinical case series)

    Open source

Product FAQ

Questions buyers ask about IGF-1 LR3

What analytical package is appropriate for IGF-1 LR3?+

Confirm the complete 83-residue sequence, intact and reduced mass, peptide mapping or another orthogonal identity method, the three native disulfide bonds, chromatographic and electrophoretic purity, aggregates and fragments, and protein content. A qualified receptor or cell-based potency assay is needed if biological activity matters. If the lot is made in E. coli, set appropriate endotoxin, host-cell protein and residual host-cell DNA limits; do not infer the expression system from the product name alone.

Why can two molecular masses be reported for the same 83-residue sequence?+

The reduced free-thiol chain has composition C₄₀₀H₆₂₅N₁₁₁O₁₁₅S₉ and an average mass of about 9,117.6 Da. Formation of three intramolecular disulfide bonds removes six hydrogens, giving C₄₀₀H₆₁₉N₁₁₁O₁₁₅S₉ and about 9,111.6 Da; Repligen’s current freeze-dried product COA uses a 9,108–9,112 Da mass-spectrometry acceptance range. A COA should state whether a theoretical or measured value is average or monoisotopic and whether it refers to reduced or disulfide-bonded material.

Evidence before order

Buyer intelligence