Gene-specific Break Apart Probe-CHURC1-FNTB

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Catalog:	GBAFP-CHURC1-FNTB-11019
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CHURC1-FNTB). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent.
Application:	CHURC1-FNTB Gene-specific Break Apart Probe is designed to detect potential CHURC1-FNTB rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	Within 10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name	CHURC1-FNTB Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]
Gene Symbol	CHURC1-FNTB
Location	14q23.3
Chromosome	Chromosome14
Coordinates	This gene maps to 65381078-65529373 in GRCh37 coordinates.
Species	Human

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