Profile: Cytocell Ltd. provides DNA screening solutions for fast and accurate detection of human genetic diseases in cytogenetics and cancer. Our products are Chromoprobe Multiprobe®, aquarius liquids and ancillary reagents. Our Chromoprobe Multiprobe® includes chromoprobe multiprobe® for all systems, AML/DMS system, CLL system, I system, chrome octo system and T system. Our Chromoprobe Multiprobe® ALL v2 panel has been designed to detect multiple rearrangements that occur primarily in B-cell lineage ALL in addition to several T-lineage markers. The panel can be used to rapidly determine genotype in leukaemia patients and aid in prognosis and treatment. Our aquarius liquids include heamatology probes, microdeletion probes, satellite probes and whole chromosome painting probes. Our heamatology probe mixtures are designed for fluorescence in situ hybridization of interphase cells and metaphase chromosomes from cultured peripheral blood cells or cultured bone marrow samples.
FDA Registration Number: 9710378
US Agent: Aysel Parr Heckel / Oxford Gene Technology, Inc
Phone: +1-(830)-688-3164 E-Mail:
2 Products/Services (Click for related suppliers)
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• Analyte Specific Reagents, Asr Reagents (FDA Code: MVU / 864.4020) Analyte specific reagents (ASR's) are antibodies, both polyclonal and monoclonal, specific receptor proteins, ligands, nucleic acid sequences, and similar reagents which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens. ASR's that otherwise fall within this definition are not within the scope of subpart E of this part when they are sold to: |
• Chromosome Culture Kit (FDA Code: KIQ / 864.2260) A chromosome culture kit is a device containing the necessary ingredients (e.g., Minimum Essential Media (MEM) of McCoy's 5A culture media, phytohemagglutinin, fetal calf serum, antibiotics, and heparin) used to culture tissues for diagnosis of congenital chromosome abnormalities. |