SPATA7-KTN1 Fusion FISH Probe
The SPATA7-KTN1 Fusion FISH Probe is used to confirm a fusion of the SPATA7 and KTN1 genes. The fusion of the SPATA7 and KTN1 genes has been associated with Sarcoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SPATA7-KTN1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-RERE | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-REOR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-REGO | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-REGR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-REAQ | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-ORRE | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-OROR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-ORGO | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GORE | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GOOR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GOGO | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GOGR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GRRE | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GROR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GRGO | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GRGR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-AQRE | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-AQOR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-AQGO | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-AQGR | 20 (40 μL) | 200 μL |
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| SPATA7-KTN1-20-AQAQ | 20 (40 μL) | 200 μL |
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KTN1 Gene Summary
This gene encodes an integral membrane protein that is a member of the kinectin protein family. The encoded protein is primarily localized to the endoplasmic reticulum membrane. This protein binds kinesin and may be involved in intracellular organelle motility. This protein also binds translation elongation factor-delta and may be involved in the assembly of the elongation factor-1 complex. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2012]
Gene Name: Kinectin 1
Chromosome: CHR14: 56046924 -56151302
Locus: 14q22.3
SPATA7 Gene Summary
This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Gene Name: Spermatogenesis Associated 7
Chromosome: CHR14: 88851987 -88904804
Locus: 14q31.3
Gene Diseases
The SPATA7 KTN1 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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