Gene-specific Copy Number Variation Probe-ATP13A2

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Catalog:	CNVFP-ATP13A2-01265
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ATP13A2). 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:	ATP13A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ATP13A2 genes. This product achieves the purpose of detection by hybridizing with the ATP13A2 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	ATPase 13A2
Gene Summary [Provided by RefSeq]	This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]
Gene Symbol	ATP13A2
Location	1p36.13
Chromosome	Chromosome1
Coordinates	This gene maps to 17312452-17338423 in GRCh37 coordinates.
Species	Human

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