Gene-specific Break Apart Probe-FAM47E-STBD1

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Catalog:	GBAFP-FAM47E-STBD1-12031
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (FAM47E-STBD1). 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:	FAM47E-STBD1 Gene-specific Break Apart Probe is designed to detect potential FAM47E-STBD1 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	FAM47E-STBD1 Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring FAM47E (family with sequence similarity 47, member E) and STBD1 (starch binding domain 1) genes on chromosome 4. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to frameshifts relative to the downstream gene. [provided by RefSeq, Jul 2011]
Gene Symbol	FAM47E-STBD1
Location	4q21.1
Chromosome	Chromosome4
Coordinates	This gene maps to 77172852-77232283 in GRCh37 coordinates.
Species	Human

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