STAG2-FAM49B Fusion FISH Probe
The STAG2-FAM49B Fusion FISH Probe is used to confirm a fusion of the STAG2 and FAM49B genes. The fusion of the STAG2 and FAM49B 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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STAG2-FAM49B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-RERE | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-REOR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-REGO | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-REGR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-REAQ | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-ORRE | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-OROR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-ORGO | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-ORAQ | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GORE | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GOOR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GOGO | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GOGR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GOAQ | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GRRE | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GROR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GRGO | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GRGR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-GRAQ | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-AQRE | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-AQOR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-AQGO | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-AQGR | 20 (40 μL) | 200 μL | ||
STAG2-FAM49B-20-AQAQ | 20 (40 μL) | 200 μL |
STAG2 Gene Summary
The protein encoded by this gene is a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division. Targeted inactivation of this gene results in chromatid cohesion defects and aneuploidy, suggesting that genetic disruption of cohesin is a cause of aneuploidy in human cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Name: Stromal Antigen 2
Chromosome: CHRX: 123094474 -123236505
Locus: Xq25
FAM49B Gene Summary
The Family With Sequence Similarity 49 Member B (FAM49B) gene is located on chr8 :130853715-130952000 at 8q24.21.
Gene Name: Family With Sequence Similarity 49 Member B
Chromosome: CHR8: 130853715 -130952000
Locus: 8q24.21
Gene Diseases
The STAG2 FAM49B 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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