1. Epigenetics Stem Cell/Wnt Protein Tyrosine Kinase/RTK JAK/STAT Signaling Immunology/Inflammation
  2. JAK IFNAR Interleukin Related
  3. pJAK2(1001-1013)

pJAK2(1001-1013) is a cell-penetrating peptide that corresponds to the activation loop of JAK2 tyrosine kinase and functions as a SOCS1/3antagonist. pJAK2 (1001-1013) blocks SOCS1-mediated negative regulation of immune function, and enhances the biological activity of cytokines such as IFNγ and IL6. pJAK2(1001-1013) inhibits the replication of a broad range of viruses and exerts dose-dependent protective efficacy against lethal viral infections. pJAK2(1001-1013) can be used for the study of immune regulation and infection.

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pJAK2(1001-1013)

pJAK2(1001-1013) Chemical Structure

CAS No. : 1259928-08-9

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Based on 1 publication(s) in Google Scholar

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Description

pJAK2(1001-1013) is a cell-penetrating peptide that corresponds to the activation loop of JAK2 tyrosine kinase and functions as a SOCS1/3antagonist. pJAK2 (1001-1013) blocks SOCS1-mediated negative regulation of immune function, and enhances the biological activity of cytokines such as IFNγ and IL6. pJAK2(1001-1013) inhibits the replication of a broad range of viruses and exerts dose-dependent protective efficacy against lethal viral infections. pJAK2(1001-1013) can be used for the study of immune regulation and infection[1][2][3].

In Vitro

pJAK2 (1001-1013) (50 μM) inhibits vaccinia virus replication by approximately 92% (intracellular virus yield) and 83% (extracellular virus yield)[1].
pJAK2 (1001-1013) (24 μM) inhibits EMCV growth by approximately 50%[1].
pJAK2(1001-1013) (11 μM, 22 h pretreatment) enhances the antiviral activity of suboptimal IFN-γ against encephalomyocarditis virus (EMCV) in human fibroblast WISH cells[2].
pJAK2(1001-1013) (20 μM, 30 min treatment) reverses SOCS-1-induced inhibition of IL-6-mediated STAT3 phosphorylation in SOCS-1-transfected human prostate cancer LNCaP cells[2].
pJAK2(1001-1013) (1-5 μM, 48 h) enhances IFN-γ-induced GAS promoter activity in WISH cells (transfected with pGAS-Luc reporter plasmid)[2].
pJAK2(1001-1013) (18 h pretreatment) inhibits replication of influenza A virus PR8 strain in MDCK cells[3].

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

In Vivo

pJAK2(1001-1013) (10-200 μg, i.p., once per day) demonstrates dose-dependent protective efficacy against lethal intranasal vaccinia virus or encephalomyocarditis virus (EMCV) infection in C57BL/6 mice[1].
pJAK2(1001–1013) (200 μg/mouse, i.p., on day -2, -1, and 0 relative to BSA immunization) enhances the Ag-specific immune response in C57BL/6 mice[2].
pJAK2(1001-1013) (200 μg/mouse, i.p., once daily for 1 week) demonstrates protective efficacy against lethal infection with influenza A/PR8 virus in female C57BL/6 mice[3].

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

Animal Model: C57BL/6 mice were intranasally challenged with a lethal dose of vaccinia virus or infected with encephalomyocarditis virus (EMCV) to establish a viral infection model[1]
Dosage: 10 μg, 50 μg, 200 μg
Administration: i.p., on days -2, -1, and 0 relative to virus challenge, once per day or every other day starting from day 2 post-virus infection
Result: Achieved dose-dependent protective efficacy.
Animal Model: C57BL/6 mice (used for Ag-specific immune response evaluation) were intraperitoneally injected with 50 μg bovine serum albumin (BSA) to establish an Ag-specific immune model[2]
Dosage: 200 μg/mouse
Administration: i.p., on day -2, -1, and 0 relative to BSA immunization
Result: Enhanced Ag-specific splenocyte proliferation 4 weeks post-BSA injection.
Animal Model: Mouse-adapted influenza A/PR8 virus (10×LD50 pfu in 10 μL PBS) was intranasally administered to 6-8-week-old female C57BL/6 mice, with 5 μL delivered into each nostril of lightly anesthetized mice[3]
Dosage: 200 μg/mouse
Administration: i.p., once daily for 1 week
Result: Demonstrated protective efficacy against lethal infection with influenza A/PR8 virus.
Alleviated influenza A/PR8 virus-induced morbidity in female C57BL/6 mice.
Molecular Weight

1716.82

Formula

C76H118N17O26P

CAS No.
Appearance

Solid

Color

White to off-white

Sequence

Leu-Pro-Gln-Asp-Lys-Glu-{pTyr}-Tyr-Lys-Val-Lys-Glu-Pro

Sequence Shortening

LPQDKE-{pTyr}-YKVKEP

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 : 1.89 mg/mL (1.10 mM; ultrasonic and adjust pH to 2 with 1 M HCl; 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 0.5825 mL 2.9124 mL 5.8247 mL
5 mM --- --- ---
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)

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Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

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Volume (start)

V1

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C2

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In Vivo:

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  15% Cremophor EL    85% Saline

    Solubility: 10 mg/mL (5.82 mM); Clear solution; Need ultrasonic

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

Purity: 99.89%

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 0.5825 mL 2.9124 mL 5.8247 mL 14.5618 mL
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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.

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Product Name:
pJAK2(1001-1013)
Cat. No.:
HY-P10373
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