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CD44v positive cancer stem cells are reported to be resistant to chemotherapy and radiation therapy, in part due to elevated resistance to ROS and their slow growth. Serial adoptive transfer studies have shown that these cells are highly enriched in tumorigenic potential. Thus, these cells are thought to survive therapeutic tumour mass reduction and upon epithelial mesenchymal transition seed distant metastases, ultimately leading to the lethality of both solid and hematopoietic cancers.

The transmembrane signalling protein CD44 binds through its extracellular domain to multiple extracellular matrix components including hyaluronan and fibronectin. It is encoded by 20 exons, 10 of which are variably included in the mature mRNA via alternative splicing controlled in part by the splicing factor ESRP1. These 10 exons contribute to variation in the membrane proximal extracellular domain of the protein. Certain variant isoforms have been shown to confer binding to growth factor receptors and importantly to a subunit of the cystine-glutamate antiporter responsible for replenishing intracellular GSH levels, thereby contributing to ROS resistance in some cancer stem cells.

Combinatorial splicing of the variant exons can theoretically yield 1024 different CD44 isoforms. Which of these potential isoforms are actually produced and physiologically relevant in different normal and tumorigenic contexts remains to be explored. Apart from the paucity of cancer stem cells in tumour explants and difficulty in their purification, the lack of a comprehensive set of validated variant isoform-specific antibodies has limited progress in understanding the role of CD44v in cancer stem cell biology.

Our rat anti-human CD44v9 monoclonal antibody recognizes CD44v8-10 and has been cited in numerous publications including the landmark paper mentioned above describing the association of CD44v8-10 with the cystine-glutamate transporter. It has been used in multiple applications, including immunoblot, IHC, IF, ELISA, flow cytometry, IP, MACS and photo-immunotherapy. In addition, we hope you will find useful our new RV3-conjugated magnetic bead kit for easy isolation of CD44V9 positive cancer stem cells. Finally, we carry a rat anti-mouse CD44v10-e16 that has been validated in flow cytometry and IHC.


NameHostReactivityCloneApplicationsCat No.
Anti-CD44 v10-e16RTMSRM1FC IHCCAC-LKG-M002
Anti-CD44 v9RTHuRV3Fc WB IHC(p) IF
Magnetic Cell
Separation Kit for
Human CD44v9+
RTHURV3Cancer Stem Cell