HGSNAT-MBOAT1 Fusion FISH Probe
The HGSNAT-MBOAT1 Fusion FISH Probe is used to confirm a fusion of the HGSNAT and MBOAT1 genes. The fusion of the HGSNAT and MBOAT1 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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| HGSNAT-MBOAT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-RERE | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-REOR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-REGO | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-REGR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-REAQ | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-ORRE | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-OROR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-ORGO | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GORE | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GOOR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GOGO | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GOGR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GRRE | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GROR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GRGO | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GRGR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-AQRE | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-AQOR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-AQGO | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-AQGR | 20 (40 μL) | 200 μL |
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| HGSNAT-MBOAT1-20-AQAQ | 20 (40 μL) | 200 μL |
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HGSNAT Gene Summary
This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. [provided by RefSeq, Jan 2009]
Gene Name: Heparan-alpha-glucosaminide N-acetyltransferase
Chromosome: CHR8: 42995591 -43057970
Locus: 8p11.21-p11.1
MBOAT1 Gene Summary
This gene belongs to the membrane-bound O-acetyltransferase superfamily. The encoded transmembrane protein is an enzyme that transfers organic compounds, preferably from oleoyl-CoA, to hydroxyl groups of protein targets in membranes. A translocation disrupting this gene may be associated with brachydactyly syndactyly syndrome. Alternately spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]
Gene Name: Membrane Bound O-acyltransferase Domain Containing 1
Chromosome: CHR6: 20100934 -20212670
Locus: 6p22.3
Gene Diseases
The HGSNAT MBOAT1 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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