Gene-specific Break Apart Probe-VWA3B

Add to Cart

Catalog:	GBAFP-VWA3B-18748
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (VWA3B). 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:	VWA3B Gene-specific Break Apart Probe is designed to detect potential VWA3B 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	Von Willebrand Factor A Domain Containing 3B
Gene Summary [Provided by RefSeq]	This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]
Gene Symbol	VWA3B
Location	2q11.2
Chromosome	Chromosome2
Coordinates	This gene maps to 98703594-98929410 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry