MLLT10-SLC16A1 Fusion FISH Probe
The MLLT10-SLC16A1 Fusion FISH Probe is used to confirm a fusion of the MLLT10 and SLC16A1 genes. The fusion of the MLLT10 and SLC16A1 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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| MLLT10-SLC16A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-RERE | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-REOR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-REGO | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-REGR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-REAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-ORRE | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-OROR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-ORGO | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GORE | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GOOR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GOGO | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GOGR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GRRE | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GROR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GRGO | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GRGR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-AQRE | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-AQOR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-AQGO | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-AQGR | 20 (40 μL) | 200 μL |
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| MLLT10-SLC16A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC16A1 Gene Summary
The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]
Gene Name: Solute Carrier Family 16 Member 1
Chromosome: CHR1: 113454469 -113498975
Locus: 1p13.2
MLLT10 Gene Summary
This gene encodes a transcription factor and has been identified as a partner gene involved in several chromosomal rearrangements resulting in various leukemias. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]
Gene Name: MLLT10, Histone Lysine Methyltransferase DOT1L Cofactor
Chromosome: CHR10: 21823100 -22032559
Locus: 10p12.31
Gene Diseases
The MLLT10 SLC16A1 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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