Gene-specific Copy Number Variation Probe-SLMO2-ATP5E

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Catalog:	CNVFP-SLMO2-ATP5E-19048
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLMO2-ATP5E). 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:	SLMO2-ATP5E Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLMO2-ATP5E genes. This product achieves the purpose of detection by hybridizing with the SLMO2-ATP5E 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	SLMO2-ATP5E Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring SLMO2 (slowmo homolog 2 (Drosophila)) and ATP5E (ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit) genes on chromosome 20. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Mar 2011]
Gene Symbol	SLMO2-ATP5E
Location	20q13.32
Chromosome	Chromosome20
Coordinates	This gene maps to 57603732-57617901 in GRCh37 coordinates.
Species	Human

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