Gene-specific Break Apart Probe-NAP1L3

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Catalog:	GBAFP-NAP1L3-05322
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NAP1L3). 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:	NAP1L3 Gene-specific Break Apart Probe is designed to detect potential NAP1L3 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	Nucleosome Assembly Protein 1 Like 3
Gene Summary [Provided by RefSeq]	This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010]
Gene Symbol	NAP1L3
Location	Xq21.32
Chromosome	ChromosomeX
Coordinates	This gene maps to 92925924-92928682 in GRCh37 coordinates.
Species	Human

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