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Cytocell

Summary

myProbes

Cytocell is a leading provider of innovative DNA screening solutions for fast and accurate detection of human genetic diseases in cytogenetics and cancer.

myProbes is a customized design and manufacture service which offers unique FISH probe, tailored to individual customer's needs. Under this service your requirements are taken by Cytocell, appropriate clones are selected and verified using PCR for know markers. The probes are manufactured using a large choice of different fluorescent dyes before being fully quality tested prior to dispatch to your lab.

Summary

Cytocell

Chromosomal rearrangements involving the end of the chromosomes have emerged as an important cause of genetic disease given the gene rich nature of the regions adjacent to the telomeres.  Labtech are proud to offer Cytocell's range of subtelomere specific probes which are located in the most distal region of chromosome specific DNA on each chromosome to provide the best possible specificity whilst also being applicable for routine use for the examination of enumeration and integrity.  These probes are directly labelled, ready to use and available in economical 5 test kits and

Summary

Cytocell

Labtech offer Cytocell's range of enumeration satellite probes which are chromosome specific sequences generated from highly repeated human satellite DNA located certain regions of each chromosome.  These probes allow rapid identification and enumeration of human chromosomes in interphase and metaphase cells. These probes are directly labelled, ready to use and available in economical 5 test kits.  The protocol is rapid and simple and has been developed to allow co-denaturation of the FISH probe and target DNA simultaneously.

 

Summary

LPA005 13, 18 and 21 prenatal probes normal result

Labtech offer Cytocell prenatal Fluorescence In situ Hybridisation assays, designed for the rapid and accurate detection of the most common foetal abnormalities.  The full range of Cytocell prenatal probe combinations including the complete prenatal screen used to detect all five of the most common foetal aneuploidies (Trisomy, 13, 18, 21 and aberrant copies of X and Y).  We also offer Cytocell's FAST FISH prenatal range which are designed to reduce the hybridisation time to just 2 hours.

 

Features And Benefits

Summary

www.labtech.co.uk

Labtech offer Cytocell's full range of painting probes.  These consist of libraries of DNA sequences derived from flow-sorted chromosomes.  These libraries contain sequences stretching over the entire length of the chromosome and provide superior coverage over each chromosome.

 

These probes are directly labelled, ready to use and available in economical 5 test kits.  The protocol is rapid and simple and has been developed to allow co-denaturation of the FISH probe and target DNA simultaneously.

 

Summary

LPU014 DiGeorge TBX1/22q13.3 combination – normal result

Microdeletion syndromes are a heterogeneous group of disorders brought about by the deletion of specific regions of chromosomal DNA causing haploinsufficiencies of important genes.  Labtech offer Cytocell's comprehensive range of microdeletion probes features products of some of the rarest human genetic syndromes.These probes are directly labelled, ready to use and available in economical 5 and 10 test kits.  The protocol is rapid and simple and has been developed to allow co-denaturation of the FISH probe and target DNA simultaneously.

 

Summary

LPH052 ATM/p53 normal result

Fluorescence In Situ Hybridisation using locus-specific probes which are capable of defining stereotypic structural rearrangements has now become a routine diagnostic test in the clinical laboratory.

Summary

Cytocell

Innovative DNA screening solutions for fast and accurate detection of human genetic diseases in cytogenetics and cancer.

Cytocell offers multiprobe devices specifically designed to look at the most common abnormalities in ALL, CLL and AML/MDS. There is also a multiprobe device designed to look at satellites on each chromosome, telomeres on each chromosome and each chromosome to be painted.

Features And Benefits