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  3. Pasotuxizumab

Pasotuxizumab  (Synonyms: BAY 2010112; AMG 212; MT112)

製品番号: HY-P99802 純度: 99.79%
COA Technical Support

Pasotuxizumab (BAY 2010112) is a PSMA and CD3 bispecific T-cell engager (BiTE). Pasotuxizumab binds to CD3 and PSMA with KDs of 9.4 nM and 47.0 nM for human CD3 and PSMA. Pasotuxizumab can be used for research of metastatic castration-resistant prostate cancer (mCRPC).

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研究用途以外に使用した場合、当社は一切の責任を負いかねます。

CAS 番号 : 1442657-12-6

容量 価格(税別) 在庫状況 数量
1 mg $450 在庫あり
5 mg $1170 在庫あり
10 mg $1870 在庫あり
50 mg   お問い合わせ  
100 mg   お問い合わせ  

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

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Based on 1 publication(s) in Google Scholar

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製品説明

Pasotuxizumab (BAY 2010112) is a PSMA and CD3 bispecific T-cell engager (BiTE). Pasotuxizumab binds to CD3 and PSMA with KDs of 9.4 nM and 47.0 nM for human CD3 and PSMA. Pasotuxizumab can be used for research of metastatic castration-resistant prostate cancer (mCRPC)[1][2].

Isotype

(scFv-heavy-kappa)-(scFv-heavy-lambda)

Species Reactivity

Human

IC50 & Target

CD3E & FOLH1

体外実験

Pasotuxizumab (0-100 ng/mL approximately, 48 h) leads to activation of CD4+ and CD8+ T cell populations, with EC50s of 3.4-6.7 ng/mL for human cocultures, and 13.7-21.2 ng/mL for cynomolgus monkey cell cocultures[2].
Pasotuxizumab (0-100 ng/mL approximately, 48 h) increases release of interferon-γ, TNF-α, IL-2 and IL-10 in T cells[2].

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

体内実験

Pasotuxizumab (0-100 ng/mL approximately, 48 h) leads to activation of CD4+ and CD8+ T cell populations, with EC50s of 3.4-6.7 ng/mL for human cocultures, and 13.7-21.2 ng/mL for cynomolgus monkey cell cocultures[2].
Pasotuxizumab (0-100 ng/mL approximately, 48 h) increases release of interferon-γ, TNF-α, IL-2 and IL-10 in T cells[2].

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

Animal Model: PC-3-huPSMA mouse xenograft model[2]
Dosage: 0.005-5 mg/kg
Administration: i.v., once daily
Result: Inhibited tumor growth by 86% (0.005 mg/kg/d) and 99% (5 mg/kg/d).
Animal Model: BALB/c mice (PK Assay)[2]
Dosage: 0.1, 0.3, and 1 mg/kg
Administration: i.v. bolus administration or s.c.
Result: Pharmacokinetic profile of Rafivirumab.
Dose (mg/kg) AUC (mg h/L) CLmatrix (L/h/kg) T1/2 (h) F (%)
i.v. (0.3) 0.93 0.32 9.7 100
s.c. (0.3) 0.17 11 18
臨床実験
Gene ID

916  [NCBI] & 2346  [NCBI]

Accession
Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

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

分子量

53.55 kDa

CAS 番号
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Pasotuxizumab]

輸送条件

Shipping with dry ice.

Formulation

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

保管条件

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

Format
  • (scFv-heavy-kappa)-(scFv-heavy-lambda)
Biological Activity
  • Immobilized PSMA Protein, Human (HEK293, His, HY-P70548A) can bind Pasotuxizumab. The EC50 for this effect is 315.4 ng/mL.
  • Immobilized CD3D-CD3E Heterodimer Protein, Human (HEK293, His, HY-P72726) can bind Pasotuxizumab. The EC50 for this effect is 6.564 ng/mL.
純度とドキュメンテーション

純度: 99.79%

参考文献
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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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Inquiry Information

製品名:
Pasotuxizumab
製品番号:
HY-P99802
数量:
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