1. Cytoskeleton Apoptosis PI3K/Akt/mTOR
  2. Integrin Apoptosis Akt
  3. Etaracizumab

Etaracizumab  (Synonyms: LM 609; MEDI 523; Anti-αvβ3 Integrin Recombinant Antibody)

Cat. No.: HY-P99291 Purity: ≥99.0%
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Etaracizumab (LM 609) is an αvβ3 integrin IgG mAb. Etaracizumab is developed to target αvβ3+ cancer cells via NK cell-mediated cytotoxicity. Etaracizumab sterically hinders access of large ligands to the RGD-binding pocket, without obstructing it. Etaracizumab decreases p-Akt in vitro. Etaracizumab can decrease cancer proliferation and invasion. Etaracizumab induces tumor cell apoptosis, and inhibition ofαvβ3-mediated cell adhesion, endothelial cell migration and osteoclast-mediated bone resorption. Etaracizumab can be studied in anti-tumor research against cancers such as ovarian cancer, metastatic melanoma as well as advanced solid tumors. Recommend Isotype Control: Human IgG1 kappa, Isotype Control (HY-P99001).

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

CAS No. : 892553-42-3

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Description

Etaracizumab (LM 609) is an αvβ3 integrin IgG mAb. Etaracizumab is developed to target αvβ3+ cancer cells via NK cell-mediated cytotoxicity. Etaracizumab sterically hinders access of large ligands to the RGD-binding pocket, without obstructing it. Etaracizumab decreases p-Akt in vitro. Etaracizumab can decrease cancer proliferation and invasion. Etaracizumab induces tumor cell apoptosis, and inhibition ofαvβ3-mediated cell adhesion, endothelial cell migration and osteoclast-mediated bone resorption. Etaracizumab can be studied in anti-tumor research against cancers such as ovarian cancer, metastatic melanoma as well as advanced solid tumors. Recommend Isotype Control: Human IgG1 kappa, Isotype Control (HY-P99001)[1][2][3][4][5].

In Vitro

Etaracizumab (24 h) decreases the degree of p-Akt by 39% in the SKOV3ip1 cells[4].
Etaracizumab (100 μg/mL, 5 d) significantly inhibits growth of ovarian cancer cells in the presence of Vitronectin (HY-P2452)-coating[4].
Etaracizumab (1-10 μg/mL, 24 h) significantly inhibits ovarian cancer cell invasion[4].

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

In Vivo

Etaracizumab (10 mg/kg, i.p., twice per week) inhibits tumor growth in orthotopic mouse model of ovarian cancer[4].

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

Animal Model: Orthotopic mouse model of advanced ovarian cancer in three cell lines (SKOV3ip1, A2780ip2, and Hey8)[4]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection (i.p.), twice per week
Result: Reduced tumor growth by 48.8% compared to IgG control in the SKOV3ip1 model.
Significantly reduced tumor growth by 83.3% when combined with Paclitaxel (HY-B0015) compared to control IgG alone in the SKOV3ip1 model.
Significantly reduced tumor growth by 86.4% when combined with Paclitaxel compared to control in the A2780ip2 model.
Significantly reduced tumor weight by 35.6% in the HeyA8 model.
Clinical Trial
Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

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

Molecular Weight

146.64 kDa

CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Etaracizumab]

Shipping

Shipping with dry ice.

Storage

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

Format
  • Human IgG1 kappa
Purity & Documentation

Purity: ≥99.0%

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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Etaracizumab
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HY-P99291
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