Gene-specific Copy Number Variation Probe-MYL2

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Catalog:	CNVFP-MYL2-13725
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYL2). 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:	MYL2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYL2 genes. This product achieves the purpose of detection by hybridizing with the MYL2 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 2
Gene Summary [Provided by RefSeq]	Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
Gene Symbol	MYL2
Location	12q24.11
Chromosome	Chromosome12
Coordinates	This gene maps to 111348623-111358404 in GRCh37 coordinates.
Species	Human

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