Gene-specific Copy Number Variation Probe-MYL3

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Catalog:	CNVFP-MYL3-13724
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYL3). 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:	MYL3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYL3 genes. This product achieves the purpose of detection by hybridizing with the MYL3 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	Myosin Light Chain 3
Gene Summary [Provided by RefSeq]	MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
Gene Symbol	MYL3
Location	3p21.31
Chromosome	Chromosome3
Coordinates	This gene maps to 46899356-46904973 in GRCh37 coordinates.
Species	Human

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