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FNDC3A-RB1 Fusion FISH Probe

The FNDC3A-RB1 Fusion FISH Probe is used to confirm a fusion of the FNDC3A and RB1 genes. The fusion of the FNDC3A and RB1 genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma, and Breast Invasive 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
FNDC3A-RB1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FNDC3A-RB1-20-RERE 20 (40 μL) 200 μL
FNDC3A-RB1-20-REOR 20 (40 μL) 200 μL
FNDC3A-RB1-20-REGO 20 (40 μL) 200 μL
FNDC3A-RB1-20-REGR 20 (40 μL) 200 μL
FNDC3A-RB1-20-REAQ 20 (40 μL) 200 μL
FNDC3A-RB1-20-ORRE 20 (40 μL) 200 μL
FNDC3A-RB1-20-OROR 20 (40 μL) 200 μL
FNDC3A-RB1-20-ORGO 20 (40 μL) 200 μL
FNDC3A-RB1-20-ORAQ 20 (40 μL) 200 μL
FNDC3A-RB1-20-GORE 20 (40 μL) 200 μL
FNDC3A-RB1-20-GOOR 20 (40 μL) 200 μL
FNDC3A-RB1-20-GOGO 20 (40 μL) 200 μL
FNDC3A-RB1-20-GOGR 20 (40 μL) 200 μL
FNDC3A-RB1-20-GOAQ 20 (40 μL) 200 μL
FNDC3A-RB1-20-GRRE 20 (40 μL) 200 μL
FNDC3A-RB1-20-GROR 20 (40 μL) 200 μL
FNDC3A-RB1-20-GRGO 20 (40 μL) 200 μL
FNDC3A-RB1-20-GRGR 20 (40 μL) 200 μL
FNDC3A-RB1-20-GRAQ 20 (40 μL) 200 μL
FNDC3A-RB1-20-AQRE 20 (40 μL) 200 μL
FNDC3A-RB1-20-AQOR 20 (40 μL) 200 μL
FNDC3A-RB1-20-AQGO 20 (40 μL) 200 μL
FNDC3A-RB1-20-AQGR 20 (40 μL) 200 μL
FNDC3A-RB1-20-AQAQ 20 (40 μL) 200 μL

RB1 Gene Summary

The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]

Gene Name: RB Transcriptional Corepressor 1

Chromosome: CHR13: 48877882 -49056026

Locus: 13q14.2

FNDC3A Gene Summary

The Fibronectin Type III Domain Containing 3A (FNDC3A) gene is located on chr13 :49550047-49783915 at 13q14.2.

Gene Name: Fibronectin Type III Domain Containing 3A

Chromosome: CHR13: 49550047 -49783915

Locus: 13q14.2

Gene Diseases

The FNDC3A RB1 Fusion has been associated with the following diseases:

Disease Name
Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

The Utility of ERBB4 and RB1 Immunohistochemistry in Distinguishing Chromophobe Renal Cell Carcinoma From Renal Oncocytoma

Renal oncocytoma (RO) is a benign epithelial neoplasm that makes up about 5 to 9% of all renal cell tumors. RO can be difficult to distinguish from a closely related but malignant counterpart, chromophobe renal cell carcinoma (ChrCC). This study used both IHC and FISH to detect the presence of RB1 and ERBB4, two genes that have been found deleted in ChrCC but not RO. A total of 28 ChrCCs and 25 RO cases were tested. Empire Genomics’ RB1 and ERBB4 FISH probes were used to detect deletions in these genes.