Gene-specific Copy Number Variation Probe-CHKB-CPT1B

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Catalog:	CNVFP-CHKB-CPT1B-02648
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CHKB-CPT1B). 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:	CHKB-CPT1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CHKB-CPT1B genes. This product achieves the purpose of detection by hybridizing with the CHKB-CPT1B 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	CHKB-CPT1B Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	The genes CHKB and CPT1B are adjacent on chromosome 22 and read-through transcripts are expressed that include exons from both loci. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to express proteins. [provided by RefSeq, Jun 2009]
Gene Symbol	CHKB-CPT1B
Location	22q13.33
Chromosome	Chromosome22
Coordinates	This gene maps to 51007289-51021428 in GRCh37 coordinates.
Species	Human

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