1. JAK/STAT Signaling Protein Tyrosine Kinase/RTK PI3K/Akt/mTOR MAPK/ERK Pathway Stem Cell/Wnt Epigenetics Cell Cycle/DNA Damage Apoptosis
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  3. Patritumab

Patritumab  (Synonyms: AMG-888; U3-1287)

Cat. No.: HY-P99275 Purity: 99.28%
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Patritumab (Human Anti-ERBB3 Recombinant Antibody) is a neutralizing monoclonal antibody to ERBB3. Patritumab shows a synergy with Cetuximab (HY-P9905), potently inhibits the phosphorylation of EGFR, HER2, HER3, ERK, and AKT. Patritumab also induces cell apoptosis and suppresses the growth of pancreatic, non-small cell lung cancer, and colorectal cancer xenograft tumors.

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

CAS No. : 1262787-83-6

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Customer Review

Based on 1 publication(s) in Google Scholar

Top Publications Citing Use of Products

1 Publications Citing Use of MCE Patritumab

WB

    Patritumab purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2024 Apr 15;30(8):1530-1543.  [Abstract]

    Patritumab (10 μM; 2 h) reduced pHER3 after NRG1 stimulation (100 ng/mL; 15 min) in CWR-R1 cells.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Patritumab (Human Anti-ERBB3 Recombinant Antibody) is a neutralizing monoclonal antibody to ERBB3. Patritumab shows a synergy with Cetuximab (HY-P9905), potently inhibits the phosphorylation of EGFR, HER2, HER3, ERK, and AKT. Patritumab also induces cell apoptosis and suppresses the growth of pancreatic, non-small cell lung cancer, and colorectal cancer xenograft tumors[1].

    Isotype

    Human IgG1(K214R) kappa

    Recommend Isotype Controls
    Species Reactivity

    Human

    IC50 & Target

    ERBB3/HER3

    In Vitro

    Patritumab targets to the extracellular domain (ECD) of HER3 and (10 μg/mL; 5 d) induces DiFi-HRG4 cells apoptosis[1].
    Patritumab (10 μg/mL; 6 h) markedly inhibits the phosphorylation of HER3 and AKT, without affecting that of ERK, in DiFi-HRG4 cells[1].
    Patritumab (10 μg/mL; 48 h) also induces the cleavage of PARP accompanied with both up-regulation of BIM and down-regulation of survivin expression[1].

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

    Western Blot Analysis[1]

    Cell Line: DiFi-HRG cells
    Concentration: 10 μg/mL
    Incubation Time: 6 hours
    Result: Inhibited the phosphorylation of HER3 and AKT as well as down-regulated survivin expression.
    In Vivo

    Patritumab (1 mg/mouse; i.p.; twice a week for 4 weeks) combines with 1 mg Cetuximab and restores Cetuximab sensitivity in DiFi-HRG tumor xenografts model in mice[1].
    Heregulin produced by colorectal cancer tumors harboring wild-type KRAS induces Cetuximab resistance, and that combination therapy with cetuximab and patritumab overcomes such resistance in vivo[1].

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

    Animal Model: Female athymic nude mice (BALB/c; 5-6 weeks old) with DiFi-Mock1 or DiFi-HRG4 (s.c.)[1]
    Dosage: 1 mg/body
    Administration: Intraperitoneal injection; twice a week for 4 weeks
    Result: Individual Patritumab treatment had little effect on the growth of tumors formed by either cell line.
    Combination of Cetuximab and Patritumab induced substantial regression of DiFi-HRG4 xenografts.
    Clinical Trial
    Gene ID

    2065  [NCBI]

    Accession
    Application

    ELISA, FACS, Functional assay

    Conjugated

    Unconjugated

    Reconsititution

    The product can be reconstituted/diluted with sterile PBS or saline.

    Molecular Weight

    146.86 kDa

    CAS No.
    Appearance

    Liquid

    Color

    Colorless to light yellow

    SMILES

    [Patritumab]

    Shipping

    Shipping with dry ice.

    Formulation

    Please refer to the lot-specific COA for specific buffer information.

    Storage

    Please store the product under the recommended conditions in the Certificate of Analysis.

    Format
    • Human IgG1 kappa
    Biological Activity
    • Flow cytometric analysis of 1×106 MCF-7 cells labelling HER3 (red) with Patritumab (HY-P99275). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then stained with the primary antibody at 1/200 dilution for an hour at 4℃. Alexa Goat Anti-Human IgG H&L (AF488) (HY-P83776) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Human IgG1(K214R) kappa Isotype Control (HY-P99995, blue) was used as the isotype control.
    • Immobilized Human HER3/ERBB3 Protein (ECD, His Tag) can bind Patritumab. The EC50 for this effect is 1.41 ng/mL.
    • Loaded Patritumab on AHC2 biosensor, can bind HER3 Protein, Human (HEK293, His, HY-P72625) with an affinity constant of 1.804E-09 M as determined in BLI assay.
    Purity & Documentation

    Purity: 99.28%

    References
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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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