Gene-specific Copy Number Variation Probe-MYCN

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Catalog:	CNVFP-MYCN-13698
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYCN). 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:	MYCN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYCN genes. This product achieves the purpose of detection by hybridizing with the MYCN 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	MYCN Proto-oncogene, BHLH Transcription Factor
Gene Summary [Provided by RefSeq]	This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]
Gene Symbol	MYCN
Location	2p24.3
Chromosome	Chromosome2
Coordinates	This gene maps to 16080682-16087129 in GRCh37 coordinates.
Species	Human

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