SEARCH OUR PRODUCT CATALOG

FAM168A-PXDNL Fusion FISH Probe

The FAM168A-PXDNL Fusion FISH Probe is used to confirm a fusion of the FAM168A and PXDNL genes. The fusion of the FAM168A and PXDNL genes has been associated with Skin Cutaneous Melanoma, and Skin Cutaneous Melanoma. 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.

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

SKU Test Kits Buffer Dye Color Order Now
FAM168A-PXDNL-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAM168A-PXDNL-20-RERE 20 (40 μL) 200 μL
FAM168A-PXDNL-20-REOR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-REGO 20 (40 μL) 200 μL
FAM168A-PXDNL-20-REGR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-REAQ 20 (40 μL) 200 μL
FAM168A-PXDNL-20-ORRE 20 (40 μL) 200 μL
FAM168A-PXDNL-20-OROR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-ORGO 20 (40 μL) 200 μL
FAM168A-PXDNL-20-ORAQ 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GORE 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GOOR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GOGO 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GOGR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GOAQ 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GRRE 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GROR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GRGO 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GRGR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-GRAQ 20 (40 μL) 200 μL
FAM168A-PXDNL-20-AQRE 20 (40 μL) 200 μL
FAM168A-PXDNL-20-AQOR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-AQGO 20 (40 μL) 200 μL
FAM168A-PXDNL-20-AQGR 20 (40 μL) 200 μL
FAM168A-PXDNL-20-AQAQ 20 (40 μL) 200 μL

FAM168A Gene Summary

The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.

Gene Name: Family With Sequence Similarity 168 Member A

Chromosome: CHR11: 73117027 -73309228

Locus: 11q13.4

PXDNL Gene Summary

The Peroxidasin Like (PXDNL) gene is located on chr8 :52232136-52722005 at 8q11.22-q11.23.

Gene Name: Peroxidasin Like

Chromosome: CHR8: 52232136 -52722005

Locus: 8q11.22-q11.23

Gene Diseases

The FAM168A PXDNL Fusion has been associated with the following diseases:

Disease Name
Skin Cutaneous Melanoma
Skin Cutaneous Melanoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.