Gene-specific Copy Number Variation Probe-CCDC169-SOHLH2

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Catalog:	CNVFP-CCDC169-SOHLH2-02052
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CCDC169-SOHLH2). 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:	CCDC169-SOHLH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CCDC169-SOHLH2 genes. This product achieves the purpose of detection by hybridizing with the CCDC169-SOHLH2 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	CCDC169-SOHLH2 Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring C13orf38 (chromosome 13 open reading frame 38) and SOHLH2 (spermatogenesis and oogenesis specific basic helix-loop-helix 2) genes. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]
Gene Symbol	CCDC169-SOHLH2
Location	13q13.3
Chromosome	Chromosome13
Coordinates	This gene maps to 36742344-36871992 in GRCh37 coordinates.
Species	Human

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