Gene-specific Break Apart Probe-EPM2AIP1

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Catalog:	GBAFP-EPM2AIP1-02373
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (EPM2AIP1). 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:	EPM2AIP1 Gene-specific Break Apart Probe is designed to detect potential EPM2AIP1 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	EPM2A Interacting Protein 1
Gene Summary [Provided by RefSeq]	The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]
Gene Symbol	EPM2AIP1
Location	3p22.2
Chromosome	Chromosome3
Coordinates	This gene maps to 37027356-37034795 in GRCh37 coordinates.
Species	Human

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