Gene-specific Break Apart Probe-STX16-NPEPL1

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Catalog:	GBAFP-STX16-NPEPL1-17894
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (STX16-NPEPL1). 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:	STX16-NPEPL1 Gene-specific Break Apart Probe is designed to detect potential STX16-NPEPL1 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	STX16-NPEPL1 Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring syntaxin 16 (STX16) and aminopeptidase-like 1 (NPEPL1) genes on chromosome 20. 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, Mar 2011]
Gene Symbol	STX16-NPEPL1
Location	20q13.32
Chromosome	Chromosome20
Coordinates	This gene maps to 57226308-57290900 in GRCh37 coordinates.
Species	Human

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