MIPOL1-SCFD1 Fusion FISH Probe
The MIPOL1-SCFD1 Fusion FISH Probe is used to confirm a fusion of the MIPOL1 and SCFD1 genes. The fusion of the MIPOL1 and SCFD1 genes has been associated with Skin Cutaneous Melanoma. 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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MIPOL1-SCFD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-RERE | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-REOR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-REGO | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-REGR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-REAQ | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-ORRE | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-OROR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-ORGO | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-ORAQ | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GORE | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GOOR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GOGO | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GOGR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GOAQ | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GRRE | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GROR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GRGO | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GRGR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-GRAQ | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-AQRE | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-AQOR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-AQGO | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-AQGR | 20 (40 μL) | 200 μL | ||
MIPOL1-SCFD1-20-AQAQ | 20 (40 μL) | 200 μL |
SCFD1 Gene Summary
The Sec1 Family Domain Containing 1 (SCFD1) gene is located on chr14 :31091520-31205018 at 14q12.
Gene Name: Sec1 Family Domain Containing 1
Chromosome: CHR14: 31091520 -31205018
Locus: 14q12
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 MIPOL1 SCFD1 Fusion has been associated with the following diseases:
Disease Name |
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Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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