Gene-specific Copy Number Variation Probe-TNFSF12-TNFSF13

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Catalog:	CNVFP-TNFSF12-TNFSF13-21206
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFSF12-TNFSF13). 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:	TNFSF12-TNFSF13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFSF12-TNFSF13 genes. This product achieves the purpose of detection by hybridizing with the TNFSF12-TNFSF13 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	TNFSF12-TNFSF13 Readthrough
Gene Summary [Provided by RefSeq]	This gene encodes a member of the tumor necrosis factor superfamily. It encodes a hybrid protein composed of the cytoplasmic and transmembrane domains of family member 12 fused to the C-terminal domain of family member 13. The hybrid protein is membrane anchored and presents the receptor-binding domain of family member 13 at the cell surface. It stimulates cycling in T- and B-lymphoma cell lines. [provided by RefSeq, Jul 2008]
Gene Symbol	TNFSF12-TNFSF13
Location	17p13.1
Chromosome	Chromosome17
Coordinates	This gene maps to 7452374-7464925 in GRCh37 coordinates.
Species	Human

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