SPTLC2-DIAPH3 Fusion FISH Probe
The SPTLC2-DIAPH3 Fusion FISH Probe is used to confirm a fusion of the SPTLC2 and DIAPH3 genes. The fusion of the SPTLC2 and DIAPH3 genes has been associated with Stomach Adenocarcinoma. 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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| SPTLC2-DIAPH3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-RERE | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-REOR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-REGO | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-REGR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-REAQ | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-ORRE | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-OROR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-ORGO | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-ORAQ | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GORE | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GOOR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GOGO | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GOGR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GOAQ | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GRRE | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GROR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GRGO | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GRGR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-GRAQ | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-AQRE | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-AQOR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-AQGO | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-AQGR | 20 (40 μL) | 200 μL |
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| SPTLC2-DIAPH3-20-AQAQ | 20 (40 μL) | 200 μL |
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SPTLC2 Gene Summary
This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011]
Gene Name: Serine Palmitoyltransferase Long Chain Base Subunit 2
Chromosome: CHR14: 77972339 -78083110
Locus: 14q24.3
DIAPH3 Gene Summary
This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Gene Name: Diaphanous Related Formin 3
Chromosome: CHR13: 60239722 -60738119
Locus: 13q21.2
Gene Diseases
The SPTLC2 DIAPH3 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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