Gene-specific Copy Number Variation Probe-ULK2

Add to Cart

Catalog:	CNVFP-ULK2-22749
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ULK2). 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:	ULK2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ULK2 genes. This product achieves the purpose of detection by hybridizing with the ULK2 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	Unc-51 Like Autophagy Activating Kinase 2
Gene Summary [Provided by RefSeq]	This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]
Gene Symbol	ULK2
Location	17p11.2
Chromosome	Chromosome17
Coordinates	This gene maps to 19674142-19771239 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry