Gene-specific Copy Number Variation Probe-B9D1

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Catalog:	CNVFP-B9D1-01122
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (B9D1). 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:	B9D1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to B9D1 genes. This product achieves the purpose of detection by hybridizing with the B9D1 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	B9 Domain Containing 1
Gene Summary [Provided by RefSeq]	This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
Gene Symbol	B9D1
Location	17p11.2
Chromosome	Chromosome17
Coordinates	This gene maps to 19240866-19281495 in GRCh37 coordinates.
Species	Human

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