Gene-specific Copy Number Variation Probe-SEPT5-GP1BB

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Catalog:	CNVFP-SEPT5-GP1BB-18233
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SEPT5-GP1BB). 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:	SEPT5-GP1BB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SEPT5-GP1BB genes. This product achieves the purpose of detection by hybridizing with the SEPT5-GP1BB 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	SEPT5-GP1BB Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring SEPT5 (septin 5) and GP1BB (glycoprotein Ib (platelet), beta polypeptide) genes on chromosome 22. This read-through transcription arises from inefficient use of an imperfect polyA signal in the upstream SEPT5 gene, whereby transcription continues into the GP1BB gene. Alternative splicing results in multiple read-through variants. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD), and are therefore unlikely to produce protein products. [provided by RefSeq, Dec 2010]
Gene Symbol	SEPT5-GP1BB
Location	22q11.21
Chromosome	Chromosome22
Coordinates	This gene maps to 19704742-19712297 in GRCh37 coordinates.
Species	Human

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