Bombesin Receptors with Future

Bombesin receptors are a subfamily of G protein-coupled receptors and consist of three different subtypes: BB1, BB2, and BB3. The central nervous system and gastrointestinal tract exhibit a wide distribution of these receptors, which have numerous physiological and pathologic effects. What's more, bombesin receptors are among the most overexpressed receptors in cancers and have drawn widespread attention to their role in tumor growth and development. Thus, identifying the function of bombesin receptors will boost their application in cancer therapy.

Fig. 1 BN family’s molecular receptors. (Serafin & Patrycja, 2023)Fig. 1 Molecular targets (receptors) for the BN family.1,3

Our Magic™ In Vitro Cell-based Bombesin Receptor Functional Assay Service

Creative Biolabs provides a robust and effective Magic™ in vitro cell-based bombesin receptor functional assay service to satisfy global customers' diverse needs. The main idea of our Magic™ in vitro cell-based bombesin receptor functional assay service is to measure the calcium flux in response to cellular response triggered by the reaction of bombesin receptors with their ligands. As a leading GPCR functional assay provider, Creative Biolabs has years of experience and expertise in this field. At Creative Biolabs, you'll achieve ideal results at an affordable price while speeding up your project's progress.

Fig.2 The workflow of our Magic™ in vitro cell-based bombesin receptor functional assay service. (Creative Biolabs Original)

The Highlight of Our Magic™ In Vitro Cell-Based Bombesin Receptor Functional Assay Service

Multiple types of cell lines

We provide numerous range of stable expressing cell lines including but not limited to human leukemia Jurkat T cells, human melanoma A375 cell lines, MCF-7 human breast cancer cells, CHO cell lines, etc., to choose from for global customers' projects.

Reliable and reputable experiment systems

Our experimental system has years of project experience and is continually being optimized as technology advances. Together with straightforward experimental procedures, we have complete confidence that we will achieve desirable outcomes for global customers.

HIGHLIGHTS. (Creative Biolabs Original)

Competent research team

Our research team features a group of specialists with extensive professional training, practical experience, and expertise, which together with state-of-the-art technologies make us confident in presenting high-quality data to global customers.

Comprehensive customized services

We offer a comprehensive customized Magic™ in vitro cell-based bombesin receptor functional assay service. Our services cover all aspects, from sample preparation to data presentation, using the latest and most advanced technical solutions available.

Published Data

Case: This study investigated small molecules for their ability to block bombesin receptors (BB1R, BB2R, and BRS-3) in lung cancer cells. Two of these molecules demonstrated comparable binding strengths to bombesin receptors, surpassing other compounds tested. Notably, these two molecules exhibited significantly stronger inhibitory effects on the growth of non-small cell lung cancer (NSCLC) cells that express bombesin receptors, making them promising drug candidates for targeting these receptors in lung cancer treatment.

Fig.3 Cytosolic Ca2+.Fig.2 Cytoplasmic Ca2+ levels for small molecule interactions with bombesin receptors.2,3

Work with Creative Biolabs

Contact flowchart. (Creative Biolabs Original)

If you are intrigued by our Magic™ in vitro cell-based bombesin receptor functional assay service, feel free to reach out to us without delay. Our experienced scientists are eager to fulfill even the most challenging requirements and deliver the best answer for global customer satisfaction.

References

  1. Serafin, Pawel, and Patrycja Kleczkowska. "Bombesins: A New Frontier in Hybrid Compound Development." Pharmaceutics 15.11 (2023): 2597.
  2. Moody, Terry W., et al. "aM-37 and sT-36 are small Molecule Bombesin receptor antagonists." Frontiers in Endocrinology 8 (2017): 176.
  3. Distributed under Open Access License CC BY 4.0, without modification.

For Research Use Only.



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