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Gene-specific Copy Number Variation Probe-SNX13

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Catalog: CNVFP-SNX13-19519
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNX13). 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: SNX13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNX13 genes. This product achieves the purpose of detection by hybridizing with the SNX13 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Category: Copy Number Variation
Probe Kits Volume (µL): 40 μL
Quantity: 20 Tests
Hybridization Solution (µL): 200 μL
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Storage Conditions: Store at -20℃ and avoid light;
Shipping Conditions: -20℃

Gene Details

Gene Name Sorting Nexin 13
Gene Summary [Provided by RefSeq] This gene encodes a PHOX domain- and RGS domain-containing protein that belongs to the sorting nexin (SNX) family and the regulator of G protein signaling (RGS) family. The PHOX domain is a phosphoinositide binding domain, and the SNX family members are involved in intracellular trafficking. The RGS family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. The RGS domain of this protein interacts with G alpha(s), accelerates its GTP hydrolysis, and attenuates G alpha(s)-mediated signaling. Overexpression of this protein delayes lysosomal degradation of the epidermal growth factor receptor. Because of its bifunctional role, this protein may link heterotrimeric G protein signaling and vesicular trafficking. [provided by RefSeq, Jul 2008]
Gene Symbol SNX13
Location 7p21.1
Chromosome Chromosome7
Coordinates This gene maps to 17830384-17980131 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-SNX13-19519-OR 573nm 548nm
2 RE CNVFP-SNX13-19519-RE 599nm 580nm
3 GO CNVFP-SNX13-19519-GO 551nm 525nm
4 GR CNVFP-SNX13-19519-GR 515nm 491nm
5 AQ CNVFP-SNX13-19519-AQ 467nm 418nm

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