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FAM96A-SNX1 Fusion FISH Probe

The FAM96A-SNX1 Fusion FISH Probe is used to confirm a fusion of the FAM96A and SNX1 genes. The fusion of the FAM96A and SNX1 genes has been associated with Breast Invasive Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
FAM96A-SNX1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAM96A-SNX1-20-RERE 20 (40 μL) 200 μL
FAM96A-SNX1-20-REOR 20 (40 μL) 200 μL
FAM96A-SNX1-20-REGO 20 (40 μL) 200 μL
FAM96A-SNX1-20-REGR 20 (40 μL) 200 μL
FAM96A-SNX1-20-REAQ 20 (40 μL) 200 μL
FAM96A-SNX1-20-ORRE 20 (40 μL) 200 μL
FAM96A-SNX1-20-OROR 20 (40 μL) 200 μL
FAM96A-SNX1-20-ORGO 20 (40 μL) 200 μL
FAM96A-SNX1-20-ORAQ 20 (40 μL) 200 μL
FAM96A-SNX1-20-GORE 20 (40 μL) 200 μL
FAM96A-SNX1-20-GOOR 20 (40 μL) 200 μL
FAM96A-SNX1-20-GOGO 20 (40 μL) 200 μL
FAM96A-SNX1-20-GOGR 20 (40 μL) 200 μL
FAM96A-SNX1-20-GOAQ 20 (40 μL) 200 μL
FAM96A-SNX1-20-GRRE 20 (40 μL) 200 μL
FAM96A-SNX1-20-GROR 20 (40 μL) 200 μL
FAM96A-SNX1-20-GRGO 20 (40 μL) 200 μL
FAM96A-SNX1-20-GRGR 20 (40 μL) 200 μL
FAM96A-SNX1-20-GRAQ 20 (40 μL) 200 μL
FAM96A-SNX1-20-AQRE 20 (40 μL) 200 μL
FAM96A-SNX1-20-AQOR 20 (40 μL) 200 μL
FAM96A-SNX1-20-AQGO 20 (40 μL) 200 μL
FAM96A-SNX1-20-AQGR 20 (40 μL) 200 μL
FAM96A-SNX1-20-AQAQ 20 (40 μL) 200 μL

SNX1 Gene Summary

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. This endosomal protein regulates the cell-surface expression of epidermal growth factor receptor. This protein also has a role in sorting protease-activated receptor-1 from early endosomes to lysosomes. This protein may form oligomeric complexes with family members. This gene results in three transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

Gene Name: Sorting Nexin 1

Chromosome: CHR15: 64388082 -64436433

Locus: 15q22.31

FAM96A Gene Summary

The Family With Sequence Similarity 96 Member A (FAM96A) gene is located on chr15 :64364760-64386207 at 15q22.31.

Gene Name: Family With Sequence Similarity 96 Member A

Chromosome: CHR15: 64364760 -64386207

Locus: 15q22.31

Gene Diseases

The FAM96A SNX1 Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.