Gene-specific Copy Number Variation Probe-WRB-SH3BGR

Add to Cart

Catalog:	CNVFP-WRB-SH3BGR-22969
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WRB-SH3BGR). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services.
Application:	WRB-SH3BGR Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WRB-SH3BGR genes. This product achieves the purpose of detection by hybridizing with the WRB-SH3BGR gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	7-10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name	WRB-SH3BGR Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring readthrough transcription between the neighboring WRB (tryptophan rich basic protein) and SH3BGR (SH3 domain binding glutamate-rich protein) genes on chromosome 21. Readthrough transcripts may encode fusion proteins that shares sequence identity with each individual gene product. [provided by RefSeq, Apr 2017]
Gene Symbol	WRB-SH3BGR
Location	21q22.2
Chromosome	Chromosome21
Coordinates	This gene maps to 39380243-39515505 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry