Gene-specific Break Apart Probe-ATP6V1G2-DDX39B

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Catalog:	GBAFP-ATP6V1G2-DDX39B-00557
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ATP6V1G2-DDX39B). 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:	ATP6V1G2-DDX39B Gene-specific Break Apart Probe is designed to detect potential ATP6V1G2-DDX39B 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	ATP6V1G2-DDX39B Readthrough (NMD Candidate)
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) and DDX39B (DEAD box polypeptide 39B) genes located in the major histocompatibility complex class III region of chromosome 6. The read-through transcript and is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]
Gene Symbol	ATP6V1G2-DDX39B
Location	6p21.33
Chromosome	Chromosome6_ssto_hap7
Coordinates	This gene maps to 2828800-2845430 in GRCh37 coordinates.
Species	Human

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