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Bispecific Antibody Drug Conjugates (ADCs)

Emerging Trends

Bispecific antibodies (bsAbs) and antibody-drug conjugates (ADCs) are two inspiring methods to the treatment of cancers in various clinical studies. In the development of therapeutic ADCs, strategies for optimizing ADCs about antibodies mainly include enhancing specificity, affinity, and internalization. The rapid development of BsAb technology contributes to more choices of antibodies as a partner of ADCs.

Conjugating payload into BsAb to improve specificity and internalization, called bispecific ADCs (BsADCs), which may be a solution to the existing problems of endocytosis, toxicity, and drug resistance of ADCs. besides, BsADCs are also a viable route to increase tumor selectivity while retaining highly potent antitumor efficacy.

Schematic bispecific ADC

Nowadays, the research and development of the BsADCs pipeline are still in their early stage and there are few preclinical products in development.

ACROBiosystems offers a series of reagents for ADCs development, comprehensive bispecific antibody targets, and services to accelerate the BsADCs development process.

Hot Targets of BsADCs

Her2

Her3

EGF R

MUC-1

Assay Data

High bioactivity verified by SPR

Herceptin (Trastuzumab) captured on a CM5 chip via anti-human IgG Fc antibodies surface, can bind Human Her2, His Tag (Cat. No. HE2-H5225) with an affinity constant of 1.07 nM as determined in an SPR assay (Biacore T200) (Routinely tested).

Protocol

High bioactivity verified by BLI

Loaded Herceptin (Trastuzumab) on AHC Biosensor, can bind Human Her2, His Tag (Cat. No. HE2-H5225) with an affinity constant of 0.825 nM as determined in BLI assay (ForteBio Octet Red96e) (Routinely tested).

Protocol

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