Gene-specific Copy Number Variation Probe-WHRN

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Catalog:	CNVFP-WHRN-23060
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WHRN). 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:	WHRN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WHRN genes. This product achieves the purpose of detection by hybridizing with the WHRN 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	Whirlin
Gene Summary [Provided by RefSeq]	This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Gene Symbol	WHRN
Location	9q32
Chromosome	Chromosome9
Coordinates	This gene maps to 114505508-114402077 in GRCh37 coordinates.
Species	Human

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