Gene-specific Copy Number Variation Probe-ARL2-SNX15

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Catalog:	CNVFP-ARL2-SNX15-00916
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ARL2-SNX15). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services.
Application:	ARL2-SNX15 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ARL2-SNX15 genes. This product achieves the purpose of detection by hybridizing with the ARL2-SNX15 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	7-10 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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