1. Cytoskeleton Metabolic Enzyme/Protease PI3K/Akt/mTOR MAPK/ERK Pathway Stem Cell/Wnt Apoptosis
  2. Integrin Transglutaminase Akt p38 MAPK ERK Caspase Apoptosis
  3. Q-Peptide

Q-Peptide is an angiopoietin-1 derived peptide (QHREDGS). Q-Peptide interacts with β1-integrin, binds to integrins on the surface of osteoblasts, and serves as an acyl donor substrate for Streptomyces mobaraensis transglutaminase. Q-Peptide activates Akt, MAPKp42/44, ILK, ERK1/2, and downregulates caspase-3/7. Q-Peptide inhibits cell apoptosis, enhances cell adhesion and migration, and promotes osteoblast differentiation, bone matrix deposition and mineralization. Q-Peptide can be used in studies related to myocardial infarction, bone regeneration, diabetic wound repair and human induced pluripotent stem cells.

For research use only. We do not sell to patients.

Custom Peptide Synthesis

Q-Peptide

Q-Peptide Chemical Structure

CAS No. : 1361235-89-3

Size Price Stock Quantity
1 mg In-stock
5 mg In-stock
10 mg In-stock
50 mg   Get quote  
100 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 Customer Validation

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Q-Peptide is an angiopoietin-1 derived peptide (QHREDGS). Q-Peptide interacts with β1-integrin, binds to integrins on the surface of osteoblasts, and serves as an acyl donor substrate for Streptomyces mobaraensis transglutaminase. Q-Peptide activates Akt, MAPKp42/44, ILK, ERK1/2, and downregulates caspase-3/7. Q-Peptide inhibits cell apoptosis, enhances cell adhesion and migration, and promotes osteoblast differentiation, bone matrix deposition and mineralization. Q-Peptide can be used in studies related to myocardial infarction, bone regeneration, diabetic wound repair and human induced pluripotent stem cells[1][2][3][4][5].

IC50 & Target[1][3]

Akt

 

p38 MAPK

 

ERK1

 

ERK2

 

Caspase 3

 

Caspase-7

 

In Vitro

Q-Peptide (QHREDGS) (5-500 μM; 5 continuous passages, 7 days) improves human induced pluripotent stem cell (BJ1D, 0901B, IMR90) expansion and viability in feeder-dependent culture by reducing caspase-dependent apoptosis, without altering proliferation, while having no significant effect on human embryonic stem cells (H9)[1].
Q-Peptide (50 μM; 5 continuous passages) preserves the in vitro pluripotency of human induced pluripotent stem cells (BJ1D, 0901B)[1].
Q-Peptide (5-500 μM; 48h) significantly increases colony number and size in feeder-free human induced pluripotent stem cells cultured on Matrigel[1].
Q-Peptide (50 μM; 0min-24h) increases integrin-linked kinase (ILK) expression, and increases expression and activation of extracellular signal-regulated kinases 1/2 (ERK1/2) across multiple time points, without affecting AKT activation[1].
Q-Peptide (7.2-29.0 mM; 6h) dose-dependently enhances human induced pluripotent stem cell adhesion to non-adhesive PEG hydrogels, and this interaction is mediated by β1-integrins[1].
Q-Peptide (200 μM; 40 min) potently acts as a substrate for Streptomyces mobaraensis transglutaminase (STG), with a cross-linking conversion yield of 93.0%[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: human induced pluripotent stem cells
Concentration: 50 μM
Incubation Time: 0min, 30min, 1.5h, 2h, 4h, 24h
Result: Increased ILK protein expression.
Significantly upregulated ERK1/2 expression.
Showed no increase in AKT phosphorylation.
In Vivo

Q-Peptide (2.2 nmol; topical; single application) significantly accelerates diabetic wound healing in db/db mice by promoting re-epithelialization and granulation tissue formation; it is significantly superior to clinically approved collagen dressings in accelerating diabetic wound healing in db/db mice, achieving near-complete wound closure by day 21[3].
QP-derived functional peptide hydrogel (1% w/v, for local single injection) mediated mesenchymal stem cell transplantation can improve cardiac function (EF and FS), reduce infarct size, collagen content and cardiomyocyte apoptosis in rat myocardial infarction models. This treatment also elevates the survival rate of transplanted cells and promotes angiogenesis. Ctf1 pretreatment can further enhance the therapeutic effects of QP-based hydrogel mediated mesenchymal stem cell transplantation[5].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: BKS.Cg-Dock7m+/+Leprdb/J (db/db) (8-week-old male, leptin-receptor deficient type 2 diabetic, full-thickness 8-mm dorsal excisional wounds)[3]
Dosage: 2.2 nmol
5.9 nmol
Administration: topical; single application
Result: Showed faster wound closure starting on day 8.
Reduced normalized wound area significantly by day 14 compared to blank or peptide-free hydrogel controls.
Reduced epithelial gap significantly compared to controls.
Increased re-epithelialization percentage significantly compared to controls.
Enlarged granulation tissue area significantly compared to controls.
Thinned advancing epidermal tongue significantly compared to controls.
Increased total number of blood vessels in the wound significantly compared to blank and peptide-free hydrogel controls.
Was significantly superior to clinically approved collagen dressings in accelerating diabetic wound healing in db/db mice, achieving near-complete wound closure by day 21
Molecular Weight

827.80

Formula

C31H49N13O14

CAS No.
Appearance

Solid

Color

White to off-white

Sequence

Gln-His-Arg-Glu-Asp-Gly-Ser

Sequence Shortening

QHREDGS

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Sealed storage, away from moisture

Powder -80°C 2 years
-20°C 1 year

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (120.80 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.2080 mL 6.0401 mL 12.0802 mL
5 mM 0.2416 mL 1.2080 mL 2.4160 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.2080 mL 6.0401 mL 12.0802 mL 30.2005 mL
5 mM 0.2416 mL 1.2080 mL 2.4160 mL 6.0401 mL
10 mM 0.1208 mL 0.6040 mL 1.2080 mL 3.0201 mL
15 mM 0.0805 mL 0.4027 mL 0.8053 mL 2.0134 mL
20 mM 0.0604 mL 0.3020 mL 0.6040 mL 1.5100 mL
25 mM 0.0483 mL 0.2416 mL 0.4832 mL 1.2080 mL
30 mM 0.0403 mL 0.2013 mL 0.4027 mL 1.0067 mL
40 mM 0.0302 mL 0.1510 mL 0.3020 mL 0.7550 mL
50 mM 0.0242 mL 0.1208 mL 0.2416 mL 0.6040 mL
60 mM 0.0201 mL 0.1007 mL 0.2013 mL 0.5033 mL
80 mM 0.0151 mL 0.0755 mL 0.1510 mL 0.3775 mL
100 mM 0.0121 mL 0.0604 mL 0.1208 mL 0.3020 mL
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
Q-Peptide
Cat. No.:
HY-P4866
Quantity:
MCE Japan Authorized Agent: