Gene-specific Copy Number Variation Probe-TSNAX-DISC1

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Catalog:	CNVFP-TSNAX-DISC1-22282
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TSNAX-DISC1). 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:	TSNAX-DISC1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TSNAX-DISC1 genes. This product achieves the purpose of detection by hybridizing with the TSNAX-DISC1 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	TSNAX-DISC1 Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This gene represents naturally occurring read-through transcription between the neighboring TSNAX (translin-associated factor X) and DISC1 (disrupted in schizophrenia 1) genes on chromosome 1. Alternative splicing results in multiple transcript variants, all of which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to be protein-coding. These alterations in gene processing may be associated with risk for psychiatric illness, most notably, schizophrenia. [provided by RefSeq, Nov 2010]
Gene Symbol	TSNAX-DISC1
Location	1q42.2
Chromosome	Chromosome1
Coordinates	This gene maps to 231664398-232177019 in GRCh37 coordinates.
Species	Human

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