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Gene-specific Break Apart Probe-SNX15

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Catalog: GBAFP-SNX15-17571
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SNX15). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent.
Application: SNX15 Gene-specific Break Apart Probe is designed to detect potential SNX15 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services.
Quantity: 20 Tests
Probe Kits Volume (µL): 40 μL
Hybridization Solution (µL): 200 μL
Turnaround Time: Within 10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Shipping Conditions: -20℃
Storage Conditions: Store at -20℃ and avoid light;

Gene Details

Gene Name Sorting Nexin 15
Gene Summary [Provided by RefSeq] This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]
Gene Symbol SNX15
Location 11q13.1
Chromosome Chromosome11
Coordinates This gene maps to 64794879-64808044 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-SNX15-17571-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-SNX15-17571-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-SNX15-17571-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-SNX15-17571-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-SNX15-17571-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-SNX15-17571-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-SNX15-17571-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-SNX15-17571-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-SNX15-17571-REGR 599nm;515nm 580nm;491nm

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