Gene-specific Copy Number Variation Probe-STAG3L5P-PVRIG2P-PILRB

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Catalog:	CNVFP-STAG3L5P-PVRIG2P-PILRB-20141
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (STAG3L5P-PVRIG2P-PILRB). 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:	STAG3L5P-PVRIG2P-PILRB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to STAG3L5P-PVRIG2P-PILRB genes. This product achieves the purpose of detection by hybridizing with the STAG3L5P-PVRIG2P-PILRB 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	STAG3L5P-PVRIG2P-PILRB Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring readthrough transcription among the neighboring LOC101735302 (stromal antigen 3 pseudogene), LOC101752334 (poliovirus receptor related immunoglobulin domain containing pseudogene) and PILRB (paired immunoglobin-like type 2 receptor beta) genes on chromosome 7. The readthrough transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Jun 2013]
Gene Symbol	STAG3L5P-PVRIG2P-PILRB
Location	7q22.1
Chromosome	Chromosome7
Coordinates	This gene maps to 100336064-100367830 in GRCh37 coordinates.
Species	Human

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