Gene-specific Copy Number Variation Probe-SLX1A-SULT1A3

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Catalog:	CNVFP-SLX1A-SULT1A3-19022
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLX1A-SULT1A3). 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:	SLX1A-SULT1A3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLX1A-SULT1A3 genes. This product achieves the purpose of detection by hybridizing with the SLX1A-SULT1A3 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	SLX1A-SULT1A3 Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring SLX1A (SLX1 structure-specific endonuclease subunit homolog A) and SULT1A3 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3) genes on the short arm of chromosome 16. A duplicate read-through locus also exists between the SLX1B and SULT1A4 genes located approximately 730 kb upstream on the same chromosome. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2017]
Gene Symbol	SLX1A-SULT1A3
Location	16p11.2
Chromosome	Chromosome16
Coordinates	This gene maps to 30205753-30215650 in GRCh37 coordinates.
Species	Human

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