Gene-specific Copy Number Variation Probe-ZNF664-RFLNA

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Catalog:	CNVFP-ZNF664-RFLNA-23949
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ZNF664-RFLNA). 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:	ZNF664-RFLNA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ZNF664-RFLNA genes. This product achieves the purpose of detection by hybridizing with the ZNF664-RFLNA 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	ZNF664-RFLNA Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 664 (Gene ID: 144348) and refilin A (Gene ID: 144347) genes on chromosome 12. The read-through transcript produces a protein that shares sequence identity with the downstream refilin A gene product. [provided by RefSeq, Dec 2016]
Gene Symbol	ZNF664-RFLNA
Location	12q24.31
Chromosome	Chromosome12
Coordinates	This gene maps to 123973214-124316023 in GRCh37 coordinates.
Species	Human

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