Gene-specific Copy Number Variation Probe-INS-IGF2

Add to Cart

Catalog:	CNVFP-INS-IGF2-07417
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (INS-IGF2). 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:	INS-IGF2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to INS-IGF2 genes. This product achieves the purpose of detection by hybridizing with the INS-IGF2 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	INS-IGF2 Readthrough
Gene Summary [Provided by RefSeq]	This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5' region and to the IGF2 gene in the 3' region. One transcript is predicted to encode a protein which shares the N-terminus with the INS protein but has a distinct and longer C-terminus, whereas the other transcript is a candidate for nonsense-mediated decay (NMD). The transcripts are imprinted and are paternally expressed in the limb and eye. [provided by RefSeq, Jul 2008]
Gene Symbol	INS-IGF2
Location	11p15.5
Chromosome	Chromosome11
Coordinates	This gene maps to 2150341-2182439 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry