Gene-specific Copy Number Variation Probe-PRR5-ARHGAP8

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Catalog:	CNVFP-PRR5-ARHGAP8-16445
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRR5-ARHGAP8). 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:	PRR5-ARHGAP8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRR5-ARHGAP8 genes. This product achieves the purpose of detection by hybridizing with the PRR5-ARHGAP8 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	PRR5-ARHGAP8 Readthrough
Gene Summary [Provided by RefSeq]	The PRR5-ARHGAP8 mRNA is an infrequent but naturally occurring read-through transcript of the neighboring proline rich 5, renal (PRR5) and Rho GTPase activating protein 8 (ARHGAP8) genes. The resulting fusion protein contains sequence identity with each individual gene product, and it includes domains characteristic of a RhoGAP protein. The significance of this read-through transcript and the function of its protein product have not yet been determined. [provided by RefSeq, Nov 2010]
Gene Symbol	PRR5-ARHGAP8
Location	22q13.31
Chromosome	Chromosome22
Coordinates	This gene maps to 45098381-45258664 in GRCh37 coordinates.
Species	Human

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