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MLLT3-TYRP1 Fusion FISH Probe

The MLLT3-TYRP1 Fusion FISH Probe is used to confirm a fusion of the MLLT3 and TYRP1 genes. The fusion of the MLLT3 and TYRP1 genes has been associated with Brain Lower Grade Glioma. 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
MLLT3-TYRP1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MLLT3-TYRP1-20-RERE 20 (40 μL) 200 μL
MLLT3-TYRP1-20-REOR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-REGO 20 (40 μL) 200 μL
MLLT3-TYRP1-20-REGR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-REAQ 20 (40 μL) 200 μL
MLLT3-TYRP1-20-ORRE 20 (40 μL) 200 μL
MLLT3-TYRP1-20-OROR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-ORGO 20 (40 μL) 200 μL
MLLT3-TYRP1-20-ORAQ 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GORE 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GOOR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GOGO 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GOGR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GOAQ 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GRRE 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GROR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GRGO 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GRGR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-GRAQ 20 (40 μL) 200 μL
MLLT3-TYRP1-20-AQRE 20 (40 μL) 200 μL
MLLT3-TYRP1-20-AQOR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-AQGO 20 (40 μL) 200 μL
MLLT3-TYRP1-20-AQGR 20 (40 μL) 200 μL
MLLT3-TYRP1-20-AQAQ 20 (40 μL) 200 μL

MLLT3 Gene Summary

The MLLT3, Super Elongation Complex Subunit (MLLT3) gene is located on chr9 :20344967-20622514 at 9p21.3.

Gene Name: MLLT3, Super Elongation Complex Subunit

Chromosome: CHR9: 20344967 -20622514

Locus: 9p21.3

TYRP1 Gene Summary

This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq, Mar 2009]

Gene Name: Tyrosinase Related Protein 1

Chromosome: CHR9: 12693385 -12710266

Locus: 9p23

Gene Diseases

The MLLT3 TYRP1 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.