SEARCH OUR PRODUCT CATALOG

STK11-HMHA1 Fusion FISH Probe

The STK11-HMHA1 Fusion FISH Probe is used to confirm a fusion of the STK11 and HMHA1 genes. The fusion of the STK11 and HMHA1 genes has been associated with Lung Adenocarcinoma. 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
STK11-HMHA1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
STK11-HMHA1-20-RERE 20 (40 μL) 200 μL
STK11-HMHA1-20-REOR 20 (40 μL) 200 μL
STK11-HMHA1-20-REGO 20 (40 μL) 200 μL
STK11-HMHA1-20-REGR 20 (40 μL) 200 μL
STK11-HMHA1-20-REAQ 20 (40 μL) 200 μL
STK11-HMHA1-20-ORRE 20 (40 μL) 200 μL
STK11-HMHA1-20-OROR 20 (40 μL) 200 μL
STK11-HMHA1-20-ORGO 20 (40 μL) 200 μL
STK11-HMHA1-20-ORAQ 20 (40 μL) 200 μL
STK11-HMHA1-20-GORE 20 (40 μL) 200 μL
STK11-HMHA1-20-GOOR 20 (40 μL) 200 μL
STK11-HMHA1-20-GOGO 20 (40 μL) 200 μL
STK11-HMHA1-20-GOGR 20 (40 μL) 200 μL
STK11-HMHA1-20-GOAQ 20 (40 μL) 200 μL
STK11-HMHA1-20-GRRE 20 (40 μL) 200 μL
STK11-HMHA1-20-GROR 20 (40 μL) 200 μL
STK11-HMHA1-20-GRGO 20 (40 μL) 200 μL
STK11-HMHA1-20-GRGR 20 (40 μL) 200 μL
STK11-HMHA1-20-GRAQ 20 (40 μL) 200 μL
STK11-HMHA1-20-AQRE 20 (40 μL) 200 μL
STK11-HMHA1-20-AQOR 20 (40 μL) 200 μL
STK11-HMHA1-20-AQGO 20 (40 μL) 200 μL
STK11-HMHA1-20-AQGR 20 (40 μL) 200 μL
STK11-HMHA1-20-AQAQ 20 (40 μL) 200 μL

STK11 Gene Summary

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]

Gene Name: Serine/threonine Kinase 11

Chromosome: CHR19: 1205797 -1228434

Locus: 19p13.3

Gene Diseases

The STK11 HMHA1 Fusion has been associated with the following diseases:

Disease Name
Lung Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.