MLLT10-SNTG1 Fusion FISH Probe
The MLLT10-SNTG1 Fusion FISH Probe is used to confirm a fusion of the MLLT10 and SNTG1 genes. The fusion of the MLLT10 and SNTG1 genes has been associated with Breast Invasive 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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| MLLT10-SNTG1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-RERE | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-REOR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-REGO | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-REGR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-REAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-ORRE | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-OROR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-ORGO | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GORE | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GOOR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GOGO | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GOGR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GRRE | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GROR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GRGO | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GRGR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-AQRE | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-AQOR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-AQGO | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-AQGR | 20 (40 μL) | 200 μL |
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| MLLT10-SNTG1-20-AQAQ | 20 (40 μL) | 200 μL |
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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
SNTG1 Gene Summary
The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]
Gene Name: Syntrophin Gamma 1
Chromosome: CHR8: 50824596 -51705427
Locus: 8q11.21
Gene Diseases
The MLLT10 SNTG1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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