CRYM-XYLT1 Fusion FISH Probe
The CRYM-XYLT1 Fusion FISH Probe is used to confirm a fusion of the CRYM and XYLT1 genes. The fusion of the CRYM and XYLT1 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. 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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| CRYM-XYLT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-RERE | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-REOR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-REGO | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-REGR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-REAQ | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-ORRE | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-OROR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-ORGO | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GORE | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GOOR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GOGO | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GOGR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GRRE | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GROR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GRGO | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GRGR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-AQRE | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-AQOR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-AQGO | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-AQGR | 20 (40 μL) | 200 μL |
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| CRYM-XYLT1-20-AQAQ | 20 (40 μL) | 200 μL |
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CRYM Gene Summary
Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness. [provided by RefSeq, Sep 2014]
Gene Name: Crystallin Mu
Chromosome: CHR16: 21269838 -21314404
Locus: 16p12.2
XYLT1 Gene Summary
This locus encodes a xylosyltransferase enzyme. The encoded protein catalyzes transfer of UDP-xylose to serine residues of an acceptor protein substrate. This transfer reaction is necessary for biosynthesis of glycosaminoglycan chains. Mutations in this gene have been associated with increased severity of pseudoxanthoma elasticum.[provided by RefSeq, Nov 2009]
Gene Name: Xylosyltransferase 1
Chromosome: CHR16: 17196180 -17564738
Locus: 16p12.3
Gene Diseases
The CRYM XYLT1 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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