ODF2L-F8 Fusion FISH Probe
The ODF2L-F8 Fusion FISH Probe is used to confirm a fusion of the ODF2L and F8 genes. The fusion of the ODF2L and F8 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ODF2L-F8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-RERE | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-REOR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-REGO | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-REGR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-REAQ | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-ORRE | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-OROR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-ORGO | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-ORAQ | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GORE | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GOOR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GOGO | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GOGR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GOAQ | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GRRE | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GROR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GRGO | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GRGR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-GRAQ | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-AQRE | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-AQOR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-AQGO | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-AQGR | 20 (40 μL) | 200 μL |
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| ODF2L-F8-20-AQAQ | 20 (40 μL) | 200 μL |
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F8 Gene Summary
This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder. [provided by RefSeq, Jul 2008]
Gene Name: Coagulation Factor VIII
Chromosome: CHRX: 154064063 -154250998
Locus: Xq28
ODF2L Gene Summary
The Outer Dense Fiber Of Sperm Tails 2 Like (ODF2L) gene is located on chr1 :86812506-86862025 at 1p22.3.
Gene Name: Outer Dense Fiber Of Sperm Tails 2 Like
Chromosome: CHR1: 86812506 -86862025
Locus: 1p22.3
Gene Diseases
The ODF2L F8 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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