Gene-specific Copy Number Variation Probe-BORCS8-MEF2B

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Catalog:	CNVFP-BORCS8-MEF2B-01560
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BORCS8-MEF2B). 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:	BORCS8-MEF2B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BORCS8-MEF2B genes. This product achieves the purpose of detection by hybridizing with the BORCS8-MEF2B 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	BORCS8-MEF2B Readthrough
Gene Summary [Provided by RefSeq]	This gene represents numerous read-through transcripts that span GeneID:729991 and 100271849. Many read-through transcripts are predicted to be nonsense-mediated decay (NMD) candidates, and are thought to be non-coding. Some transcripts are predicted to be capable of translation reinitiation at a downstream AUG, resulting in expression of at least one isoform of myocyte enhancer factor 2B (MEF2B) from this read-through locus. At least one additional MEF2B variant and isoform can be expressed from a downstream promoter, and is annotated on GeneID:100271849. [provided by RefSeq, Oct 2010]
Gene Symbol	BORCS8-MEF2B
Location	19p13.11
Chromosome	Chromosome19
Coordinates	This gene maps to 19192590-19145566 in GRCh37 coordinates.
Species	Human

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