April 17, 2006
Research Findings Validate EpiSep XRC™ as Novel Methods for Detecting Lymph Node Metastases.
March 7, 2006
WaveSense Releases Research Products for Melanoma Cells - Expands XRC™ Portfolio
  March 1, 2006
WaveSense to Showcase New Melanoma Cell Detection Kit at 2006 AACR
   
 
 

 

 

 

 

 

 

WaveSense Releases Research Products for Melanoma Cells - Expands XRC™ Portfolio

March 7, 2006

Extending its position in the field of cellular analysis, WaveSense recently announced the availability of the EpiSep™ Melanoma (9.2.27) detection kit. The Melanoma kit utilizes WaveSense’s proprietary Xenographic Retention Chromatography™ (XRC™) technology, and a combination of four antibodies. EpiSep XRC™ is an open platform for rapid and sensitive capture and sorting of live cells, proteins, and genes for interrogation – providing ideal laboratory processes for end-users of the Melanoma kit.

The kit antibodies include; Monoclonal 9.2.27 for recognition of Melanoma-associated Chondroitin Sulfate Proteogylcan (MCSP) complex for capture on magnetic particles; and three biotin labeled monoclonal antibodies – M2-7C10, A103, and T311, which are used to detect and recognize, respectively, the Mart-1, Melan-A and Tyrosinase epitopes in melanoma cells. The combination of antibodies, in conjunction with EpiSep XRC™, provides excellent specificity and sensitivity for detection of rare cells in a variety of samples that include blood, tissue preparation, and cell culture.

The EpiSep XRC platform improves workflow procedures by seamlessly isolating and characterizing target cells from large backgrounds in a single device - eliminating cumbersome and prolonged procedures that include centrifugation, aspiration or decanting steps. Three-dimensional sampling from tissue is an additive benefit of the WaveSense platform. With respect to the Melanoma (9.2.27) XRC™ kit, the 9.2.27 antibody is directed against the 250 KD Melanoma-associated Chondroitin Sulfate Proteoglycan (MCSP), and then coated onto paramagnetic particles. The particles capture melanocytes, which are then simply and easily processed in the EpiSep™ device for detection and characterization.

WaveSense has collaborated with Drs Oystein Fodstad and Hanne Kleppe Hoifodt of the Tumor Biology Department of Radium Hospital in Oslo, Norway to evaluate the utility of the reagents. In a poster presented at the 2005 Annual Symposium on Minimal Residual Cancer in San Francisco, CA, Drs Fodstad and Hoifodt reported that:

“The method allows tumor cells in the different samples to be identified in less than 2 hours. The immuno-magnetically captured cells are pure, viable and unaltered and can be used for further immunological and molecular analysis, as well as for in vitro and in vivo cell culture.”

WaveSense will showcase its new Melanoma (9.2.27) XRC™ Kit, April 1-5th, at the 2006 annual meeting of the American Association of Cancer Research.

WaveSense develops and manufactures novel products for life science research and clinical research laboratories. The company’s extensive line of products offer robust and easy to use assays for a wide variety of life science research applications. These include rapid and sensitive cell based assays, rare cell capture and detection, and tumor cell biomarker characterization. The power of the proprietary XRC™ technology allows use of samples from a variety of sources such as blood, tissue and bone marrow.

Dr. Oystein Fodstad and Dr. Hanne Kleppe Hoifodt are affiliated with the Dept. of Tumor Biology, The Norwegian Radium Hospital in Oslo, Norway. Dr. Fodstad is also with the University of South Alabama, Cancer Research Institute in Mobile, AL. Dr.’s Fodstad and Hoifodt are regarded as world leading authorities in the field of magnetic capture and isolation of tumor cells. Professor Fodstad has recently agreed to become Chairman of WaveSense’s Scientific Advisory Board.

The products described in this announcement are for research use only and not intended for diagnostic or therapeutic purposes.

 

 

Ref. 060307-101

 
WAVESENSE EVENTS
 

American Association of Cancer Research
April 14-18, 2007
Los Angeles, CA

 
       

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