SYDE2-TCTN1 Fusion FISH Probe
The SYDE2-TCTN1 Fusion FISH Probe is used to confirm a fusion of the SYDE2 and TCTN1 genes. The fusion of the SYDE2 and TCTN1 genes has been associated with Sarcoma. 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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SYDE2-TCTN1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-RERE | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-REOR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-REGO | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-REGR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-REAQ | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-ORRE | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-OROR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-ORGO | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-ORAQ | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GORE | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GOOR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GOGO | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GOGR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GOAQ | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GRRE | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GROR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GRGO | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GRGR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-GRAQ | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-AQRE | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-AQOR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-AQGO | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-AQGR | 20 (40 μL) | 200 μL | ||
SYDE2-TCTN1-20-AQAQ | 20 (40 μL) | 200 μL |
TCTN1 Gene Summary
This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Name: Tectonic Family Member 1
Chromosome: CHR12: 111051831 -111086935
Locus: 12q24.11
SYDE2 Gene Summary
The Synapse Defective Rho GTPase Homolog 2 (SYDE2) gene is located on chr1 :85623355-85666728 at 1p22.3.
Gene Name: Synapse Defective Rho GTPase Homolog 2
Chromosome: CHR1: 85623355 -85666728
Locus: 1p22.3
Gene Diseases
The SYDE2 TCTN1 Fusion has been associated with the following diseases:
Disease Name |
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Sarcoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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