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ADT1753-Human Anti-CD3xGPRC5D Bispecific Antibody
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ADT1753-Human Anti-CD3xGPRC5D Bispecific Antibody

  • Catalog Number ADT1753
  • Host CHO Cells
  • Species Human
  • Target CD3xGPRC5D
  • Application FuncS

CD3, T cell receptor complex (including CD3 γ/δ/ε/Zeta chains), is a core signaling molecule for T cell activation. GPRC5D, G protein-coupled receptor C5D, is specifically expressed in multiple myeloma and is a novel immunotherapy target.

 

In addition to supplying high-quality bispecific antibody products, Alpha Lifetech offers comprehensive bispecific antibody development services.

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Product Background

Talquetamab is a IgG4-PAA bispecific G protein-coupled receptor class C group 5 member D (GPRC5D)-directed CD3 T-cell engager. It consists of two arms - anti-GPRC5D and anti-CD3 arms - linked by two interchain disulfide bonds, each arm comprising a heavy and light chain. Talquetamab binds to GPRC5D, a cell surface receptor expressed predominantly on multiple myeloma cells, and CD3 on T cells. It works to recruit CD3-expressing T cells to GPRC5D-expressing multiple myeloma cells to induce T-cell–mediated cytotoxicity.

Product Specification

Catalog Number

ADT1753

Product Name

ADT1753-Human Anti-CD3xGPRC5D Bispecific Antibody

Isotype

Human IgG4-kappa

Clonity

Monoclonal

Alternate Names

Human Anti-CD3 mAb, Anti-CD3 Monoclonal Antibody, CD3 recombinant antibody, Anti-CD3 Bispecific Antibody, Human Anti-GPRC5D mAb, GPRC5D recombinant antibody, Anti-GPRC5D Monoclonal Antibody, Anti-GPRC5D Bispecific Antibody

Official Symbol

CD3xGPRC5D

Target 1

CD3

Gene ID 1

916

Target 2

GPRC5D

Gene ID 2

55507

Species

Human

Drug Name

Talquetamab

Endotoxin

<1EU/mg. Determined by the LAL method.

Sterility

0.2 μM filtered.

Expression Host

CHO Cells

CAS Number

2226212-40-2

Chemical Formula

C6410H9938N1716O2006S45

Molecular Weight

147 KDa

Product Description

Talquetamab is a bispecific antibody used to treat adults with relapsed or refractory multiple myeloma.

Mechanism of Action

Talquetamab is a bispecific T-cell-engaging antibody that binds to the CD3 receptor expressed on the surface of T-cells and GPRC5D expressed on the surface of MM cells. It works to recruit CD3-expressing T cells to GPRC5D-expressing MM cells to induce T-cell–mediated cytotoxicity, prevent tumor growth, and promote tumor regression. When activated, T cells cause the release of proinflammatory cytokines, promoting the lysis of MM cells.

Metabolism

Talquetamab is expected to be metabolized into small peptides by catabolic pathways.

Size

1mg,5mg,50mg,100mg

Research Area

Cancer

Application

FuncS

Purity

>90%

Concentration

Batch dependent

Buffer

Supplied in PBS, pH 7.4,Contains no stabilizers or preservatives

Recommended Dilution Buffer

ABDB-1002 or PBS, pH 7.4, Contains no stabilizers or preservatives.

Storage

2 weeks, 2-8℃ under sterile conditions after reconstitution. Avoid repeated freeze-thaw. -80°C for one-year storage.

Shipping Condition

Shipped on ice packs.

Protocol Information

Since applications vary, each investigator should use the application references as a guide to help estimate the appropriate dose or concentration. The dose or concentration can be further optimized experimentally in a dose-response or titration experiment. 

Note

For Research Use Only!

Reference

1. Pillarisetti K, Edavettal S, Mendonca M, Li Y, Tornetta M, Babich A, Majewski N, Husovsky M, Reeves D, Walsh E, Chin D, Luistro L, Joseph J, Chu G, Packman K, Shetty S, Elsayed Y, Attar R, Gaudet F: A T-cell-redirecting bispecific G-protein-coupled receptor class 5 member D x CD3 antibody to treat multiple myeloma. Blood. 2020 Apr 9;135(15):1232-1243. doi: 10.1182/blood.2019003342.
2. Verkleij CPM, Broekmans MEC, van Duin M, Frerichs KA, Kuiper R, de Jonge AV, Kaiser M, Morgan G, Axel A, Boominathan R, Sendecki J, Wong A, Verona RI, Sonneveld P, Zweegman S, Adams HC, Mutis T, van de Donk NWCJ: Preclinical activity and determinants of response of the GPRC5DxCD3 bispecific antibody talquetamab in multiple myeloma. Blood Adv. 2021 Apr 27;5(8):2196-2215. doi: 10.1182/bloodadvances.2020003805.

 

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