ZNHIT3-WDR60 Fusion FISH Probe
The ZNHIT3-WDR60 Fusion FISH Probe is used to confirm a fusion of the ZNHIT3 and WDR60 genes. The fusion of the ZNHIT3 and WDR60 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ZNHIT3-WDR60-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-RERE | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-REOR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-REGO | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-REGR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-REAQ | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-ORRE | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-OROR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-ORGO | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-ORAQ | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GORE | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GOOR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GOGO | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GOGR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GOAQ | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GRRE | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GROR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GRGO | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GRGR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-GRAQ | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-AQRE | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-AQOR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-AQGO | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-AQGR | 20 (40 μL) | 200 μL |
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| ZNHIT3-WDR60-20-AQAQ | 20 (40 μL) | 200 μL |
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ZNHIT3 Gene Summary
The Zinc Finger HIT-type Containing 3 (ZNHIT3) gene is located on chr17 :34842472-34851662 at 17q12.
Gene Name: Zinc Finger HIT-type Containing 3
Chromosome: CHR17: 34842472 -34851662
Locus: 17q12
WDR60 Gene Summary
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) and may facilitate the formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. The encoded protein contains four WD repeats and may play a role in the formation of cilia. Mutations in this gene have been associated with short-rib polydactyly and Jeune syndromes. [provided by RefSeq, Mar 2014]
Gene Name: WD Repeat Domain 60
Chromosome: CHR7: 158649268 -158738883
Locus: 7q36.3
Gene Diseases
The ZNHIT3 WDR60 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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