Gene-specific Break Apart Probe-ARL2-SNX15

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Catalog:	GBAFP-ARL2-SNX15-10014
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ARL2-SNX15). 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:	ARL2-SNX15 Gene-specific Break Apart Probe is designed to detect potential ARL2-SNX15 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	ARL2-SNX15 Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring ADP-ribosylation factor-like 2 (ARL2) and sorting nexin 15 (SNX15) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]
Gene Symbol	ARL2-SNX15
Location	11q13.1
Chromosome	Chromosome11
Coordinates	This gene maps to 64781584-64808044 in GRCh37 coordinates.
Species	Human

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