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RUNX1T1-FAM164A Fusion FISH Probe

The RUNX1T1-FAM164A Fusion FISH Probe is used to confirm a fusion of the RUNX1T1 and FAM164A genes. The fusion of the RUNX1T1 and FAM164A genes has been associated with Esophageal 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
RUNX1T1-FAM164A-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-RERE 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-REOR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-REGO 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-REGR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-REAQ 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-ORRE 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-OROR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-ORGO 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-ORAQ 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GORE 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GOOR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GOGO 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GOGR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GOAQ 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GRRE 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GROR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GRGO 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GRGR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-GRAQ 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-AQRE 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-AQOR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-AQGO 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-AQGR 20 (40 μL) 200 μL
RUNX1T1-FAM164A-20-AQAQ 20 (40 μL) 200 μL

RUNX1T1 Gene Summary

This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]

Gene Name: RUNX1 Translocation Partner 1

Chromosome: CHR8: 92967194 -93115454

Locus: 8q21.3

Gene Diseases

The RUNX1T1 FAM164A Fusion has been associated with the following diseases:

Disease Name
Esophageal Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.