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FAM168A-P4HA3 Fusion FISH Probe

The FAM168A-P4HA3 Fusion FISH Probe is used to confirm a fusion of the FAM168A and P4HA3 genes. The fusion of the FAM168A and P4HA3 genes has been associated with Uterine Corpus Endometrial 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
FAM168A-P4HA3-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAM168A-P4HA3-20-RERE 20 (40 μL) 200 μL
FAM168A-P4HA3-20-REOR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-REGO 20 (40 μL) 200 μL
FAM168A-P4HA3-20-REGR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-REAQ 20 (40 μL) 200 μL
FAM168A-P4HA3-20-ORRE 20 (40 μL) 200 μL
FAM168A-P4HA3-20-OROR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-ORGO 20 (40 μL) 200 μL
FAM168A-P4HA3-20-ORAQ 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GORE 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GOOR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GOGO 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GOGR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GOAQ 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GRRE 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GROR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GRGO 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GRGR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-GRAQ 20 (40 μL) 200 μL
FAM168A-P4HA3-20-AQRE 20 (40 μL) 200 μL
FAM168A-P4HA3-20-AQOR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-AQGO 20 (40 μL) 200 μL
FAM168A-P4HA3-20-AQGR 20 (40 μL) 200 μL
FAM168A-P4HA3-20-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

P4HA3 Gene Summary

This gene encodes a component of prolyl 4-hydroxylase, a key enzyme in collagen synthesis composed of two identical alpha subunits and two beta subunits. The encoded protein is one of several different types of alpha subunits and provides the major part of the catalytic site of the active enzyme. In collagen and related proteins, prolyl 4-hydroxylase catalyzes the formation of 4-hydroxyproline that is essential to the proper three-dimensional folding of newly synthesized procollagen chains. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

Gene Name: Prolyl 4-hydroxylase Subunit Alpha 3

Chromosome: CHR11: 73977701 -74022699

Locus: 11q13.4

Gene Diseases

The FAM168A P4HA3 Fusion has been associated with the following diseases:

Disease Name
Uterine Corpus Endometrial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.