Gene-specific Break Apart Probe-CNFN

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Catalog:	GBAFP-CNFN-01457
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CNFN). 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:	CNFN Gene-specific Break Apart Probe is designed to detect potential CNFN 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	Cornifelin
Gene Summary [Provided by RefSeq]	The Cornifelin (CNFN) gene is located on chr19:42891170 -42894444 at 19q13.2.
Gene Symbol	CNFN
Location	19q13.2
Chromosome	Chromosome19
Coordinates	This gene maps to 42891170-42894444 in GRCh37 coordinates.
Species	Human

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