SEARCH OUR PRODUCT CATALOG

TRIM29-PAK1 Fusion FISH Probe

The TRIM29-PAK1 Fusion FISH Probe is used to confirm a fusion of the TRIM29 and PAK1 genes. The fusion of the TRIM29 and PAK1 genes has been associated with Liver Hepatocellular 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
TRIM29-PAK1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
TRIM29-PAK1-20-RERE 20 (40 μL) 200 μL
TRIM29-PAK1-20-REOR 20 (40 μL) 200 μL
TRIM29-PAK1-20-REGO 20 (40 μL) 200 μL
TRIM29-PAK1-20-REGR 20 (40 μL) 200 μL
TRIM29-PAK1-20-REAQ 20 (40 μL) 200 μL
TRIM29-PAK1-20-ORRE 20 (40 μL) 200 μL
TRIM29-PAK1-20-OROR 20 (40 μL) 200 μL
TRIM29-PAK1-20-ORGO 20 (40 μL) 200 μL
TRIM29-PAK1-20-ORAQ 20 (40 μL) 200 μL
TRIM29-PAK1-20-GORE 20 (40 μL) 200 μL
TRIM29-PAK1-20-GOOR 20 (40 μL) 200 μL
TRIM29-PAK1-20-GOGO 20 (40 μL) 200 μL
TRIM29-PAK1-20-GOGR 20 (40 μL) 200 μL
TRIM29-PAK1-20-GOAQ 20 (40 μL) 200 μL
TRIM29-PAK1-20-GRRE 20 (40 μL) 200 μL
TRIM29-PAK1-20-GROR 20 (40 μL) 200 μL
TRIM29-PAK1-20-GRGO 20 (40 μL) 200 μL
TRIM29-PAK1-20-GRGR 20 (40 μL) 200 μL
TRIM29-PAK1-20-GRAQ 20 (40 μL) 200 μL
TRIM29-PAK1-20-AQRE 20 (40 μL) 200 μL
TRIM29-PAK1-20-AQOR 20 (40 μL) 200 μL
TRIM29-PAK1-20-AQGO 20 (40 μL) 200 μL
TRIM29-PAK1-20-AQGR 20 (40 μL) 200 μL
TRIM29-PAK1-20-AQAQ 20 (40 μL) 200 μL

PAK1 Gene Summary

This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]

Gene Name: P21 (RAC1) Activated Kinase 1

Chromosome: CHR11: 77033059 -77185108

Locus: 11q13.5-q14.1

TRIM29 Gene Summary

The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype. [provided by RefSeq, Jul 2008]

Gene Name: Tripartite Motif Containing 29

Chromosome: CHR11: 119981993 -120008863

Locus: 11q23.3

Gene Diseases

The TRIM29 PAK1 Fusion has been associated with the following diseases:

Disease Name
Liver Hepatocellular Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Distinct Patterns of Acral Melanoma Based on Site and Relative Sun Exposure

Acral melanomas vary considerably in their molecular, histological, and clinical presentation. In this study, acral melanomas from dorsal, volar, and subungual-interdigital body sites were assessed using several tests, including FISH. Our TERT, CCND1, CDK4, AURKA, CDKN2A, PAK1, PTEN, NF1, and GAB2 probes were used to detect copy number variations in these genes. Genetic profiles were found to be tightly tied to UV exposure.

Distinct Patterns of Acral Melanoma Based on Site and Relative Sun Exposure

Acral melanomas vary considerably in their molecular, histological, and clinical presentation. In this study, acral melanomas from dorsal, volar, and subungual-interdigital body sites were assessed using several tests, including FISH. Our TERT, CCND1, CDK4, AURKA, CDKN2A, PAK1, PTEN, NF1, and GAB2 probes were used to detect copy number variations in these genes. Genetic profiles were found to be tightly tied to UV exposure.