Gene-specific Break Apart Probe-PRCD

Add to Cart

Catalog:	GBAFP-PRCD-16133
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PRCD). 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:	PRCD Gene-specific Break Apart Probe is designed to detect potential PRCD 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	Photoreceptor Disc Component
Gene Summary [Provided by RefSeq]	This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
Gene Symbol	PRCD
Location	17q25.1
Chromosome	Chromosome17
Coordinates	This gene maps to 74523667-74541458 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry