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TRIM2-FAM71F1 Fusion FISH Probe

The TRIM2-FAM71F1 Fusion FISH Probe is used to confirm a fusion of the TRIM2 and FAM71F1 genes. The fusion of the TRIM2 and FAM71F1 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.

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

SKU Test Kits Buffer Dye Color Order Now
TRIM2-FAM71F1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-RERE 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-REOR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-REGO 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-REGR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-REAQ 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-ORRE 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-OROR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-ORGO 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-ORAQ 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GORE 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GOOR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GOGO 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GOGR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GOAQ 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GRRE 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GROR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GRGO 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GRGR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-GRAQ 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-AQRE 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-AQOR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-AQGO 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-AQGR 20 (40 μL) 200 μL
TRIM2-FAM71F1-20-AQAQ 20 (40 μL) 200 μL

TRIM2 Gene Summary

The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic filaments. It plays a neuroprotective role and functions as an E3-ubiquitin ligase in proteasome-mediated degradation of target proteins. Mutations in this gene can cause early-onset axonal neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

Gene Name: Tripartite Motif Containing 2

Chromosome: CHR4: 154074269 -154260474

Locus: 4q31.3

FAM71F1 Gene Summary

The Family With Sequence Similarity 71 Member F1 (FAM71F1) gene is located on chr7 :128355442-128371797 at 7q32.1.

Gene Name: Family With Sequence Similarity 71 Member F1

Chromosome: CHR7: 128355442 -128371797

Locus: 7q32.1

Gene Diseases

The TRIM2 FAM71F1 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.