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KIF1B-NF1 Fusion FISH Probe

The KIF1B-NF1 Fusion FISH Probe is used to confirm a fusion of the KIF1B and NF1 genes. The fusion of the KIF1B and NF1 genes has been associated with Bladder Urothelial 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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
KIF1B-NF1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KIF1B-NF1-20-RERE 20 (40 μL) 200 μL
KIF1B-NF1-20-REOR 20 (40 μL) 200 μL
KIF1B-NF1-20-REGO 20 (40 μL) 200 μL
KIF1B-NF1-20-REGR 20 (40 μL) 200 μL
KIF1B-NF1-20-REAQ 20 (40 μL) 200 μL
KIF1B-NF1-20-ORRE 20 (40 μL) 200 μL
KIF1B-NF1-20-OROR 20 (40 μL) 200 μL
KIF1B-NF1-20-ORGO 20 (40 μL) 200 μL
KIF1B-NF1-20-ORAQ 20 (40 μL) 200 μL
KIF1B-NF1-20-GORE 20 (40 μL) 200 μL
KIF1B-NF1-20-GOOR 20 (40 μL) 200 μL
KIF1B-NF1-20-GOGO 20 (40 μL) 200 μL
KIF1B-NF1-20-GOGR 20 (40 μL) 200 μL
KIF1B-NF1-20-GOAQ 20 (40 μL) 200 μL
KIF1B-NF1-20-GRRE 20 (40 μL) 200 μL
KIF1B-NF1-20-GROR 20 (40 μL) 200 μL
KIF1B-NF1-20-GRGO 20 (40 μL) 200 μL
KIF1B-NF1-20-GRGR 20 (40 μL) 200 μL
KIF1B-NF1-20-GRAQ 20 (40 μL) 200 μL
KIF1B-NF1-20-AQRE 20 (40 μL) 200 μL
KIF1B-NF1-20-AQOR 20 (40 μL) 200 μL
KIF1B-NF1-20-AQGO 20 (40 μL) 200 μL
KIF1B-NF1-20-AQGR 20 (40 μL) 200 μL
KIF1B-NF1-20-AQAQ 20 (40 μL) 200 μL

NF1 Gene Summary

This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Neurofibromin 1

Chromosome: CHR17: 29421944 -29704695

Locus: 17q11.2

KIF1B Gene Summary

This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1. [provided by RefSeq, Jul 2008]

Gene Name: Kinesin Family Member 1B

Chromosome: CHR1: 10270763 -10441661

Locus: 1p36.22

Gene Diseases

The KIF1B NF1 Fusion has been associated with the following diseases:

Disease Name
Bladder Urothelial 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.