Gene-specific Break Apart Probe-C8ORF37

Add to Cart

Catalog:	GBAFP-C8orf37-00916
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (C8ORF37). 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:	C8ORF37 Gene-specific Break Apart Probe is designed to detect potential C8ORF37 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	Chromosome 8 Open Reading Frame 37
Gene Summary [Provided by RefSeq]	This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]
Gene Symbol	C8orf37
Location	8q22.1
Chromosome	Chromosome8
Coordinates	This gene maps to 96257140-96281462 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry