KIF21A-MIPOL1 Fusion FISH Probe
The KIF21A-MIPOL1 Fusion FISH Probe is used to confirm a fusion of the KIF21A and MIPOL1 genes. The fusion of the KIF21A and MIPOL1 genes has been associated with Lung Squamous Cell 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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| KIF21A-MIPOL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-RERE | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-REOR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-REGO | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-REGR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-REAQ | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-ORRE | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-OROR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-ORGO | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GORE | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GOOR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GOGO | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GOGR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GRRE | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GROR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GRGO | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GRGR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-AQRE | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-AQOR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-AQGO | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-AQGR | 20 (40 μL) | 200 μL |
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| KIF21A-MIPOL1-20-AQAQ | 20 (40 μL) | 200 μL |
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KIF21A Gene Summary
This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
Gene Name: Kinesin Family Member 21A
Chromosome: CHR12: 39687029 -39837192
Locus: 12q12
MIPOL1 Gene Summary
This gene encodes a coiled-coil domain-containing protein. The encoded protein may function as a tumor suppressor. A translocation that results in truncation of the protein encoded by this locus has been associated with mirror-image polydactyly, also known as Laurin-Sandrow Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2010]
Gene Name: Mirror-image Polydactyly 1
Chromosome: CHR14: 37667117 -38020464
Locus: 14q13.3-q21.1
Gene Diseases
The KIF21A MIPOL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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