Gene-specific Copy Number Variation Probe-INMT-MINDY4

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Catalog:	CNVFP-INMT-MINDY4-07397
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (INMT-MINDY4). 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:	INMT-MINDY4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to INMT-MINDY4 genes. This product achieves the purpose of detection by hybridizing with the INMT-MINDY4 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	INMT-MINDY4 Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This locus represents rare but naturally occurring read-through transcription between the INMT (indolethylamine N-methyltransferase) and FAM188B (family with sequence similarity 188, member B) genes on chromosome 7. The read-through transcript is unlikely to produce a protein because it is a nonsense-mediated mRNA decay (NMD) candidate based on translation from the supported INMT start codon. [provided by RefSeq, Nov 2010]
Gene Symbol	INMT-MINDY4
Location	7p14.3
Chromosome	Chromosome7
Coordinates	This gene maps to 30752134-30892386 in GRCh37 coordinates.
Species	Human

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