Gene-specific Break Apart Probe-CHKB-CPT1B

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Catalog:	GBAFP-CHKB-CPT1B-01302
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CHKB-CPT1B). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent.
Application:	CHKB-CPT1B Gene-specific Break Apart Probe is designed to detect potential CHKB-CPT1B rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	Within 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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