SNTB2-CHST4 Fusion FISH Probe
The SNTB2-CHST4 Fusion FISH Probe is used to confirm a fusion of the SNTB2 and CHST4 genes. The fusion of the SNTB2 and CHST4 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SNTB2-CHST4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-RERE | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-REOR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-REGO | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-REGR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-REAQ | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-ORRE | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-OROR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-ORGO | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GORE | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GOOR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GOGO | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GOGR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GRRE | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GROR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GRGO | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GRGR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-AQRE | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-AQOR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-AQGO | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-AQGR | 20 (40 μL) | 200 μL |
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| SNTB2-CHST4-20-AQAQ | 20 (40 μL) | 200 μL |
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SNTB2 Gene Summary
Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]
Gene Name: Syntrophin Beta 2
Chromosome: CHR16: 69221049 -69342955
Locus: 16q22.1
CHST4 Gene Summary
This gene encodes an N-acetylglucosamine 6-O sulfotransferase. The encoded enzyme transfers sulfate from 3'phosphoadenosine 5'phospho-sulfate to the 6-hydroxyl group of N-acetylglucosamine on glycoproteins. This protein is localized to the Golgi and is involved in the modification of glycan structures on ligands of the lymphocyte homing receptor L-selectin. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]
Gene Name: Carbohydrate Sulfotransferase 4
Chromosome: CHR16: 71560022 -71572493
Locus: 16q22.2
Gene Diseases
The SNTB2 CHST4 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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