XYLT2 Break Apart FISH Probe
Empire Genomics’ XYLT2 Break Apart FISH Probe is designed to flank the XYLT2 gene and is typically used for detecting XYLT2 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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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| XYLT2BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-GORE | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-GROR | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-REGO | 20 (40 μL) | 200 μL |
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| XYLT2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene is an isoform of xylosyltransferase, which belongs to a family of glycosyltransferases. This enzyme transfers xylose from UDP-xylose to specific serine residues of the core protein and initiates the biosynthesis of glycosaminoglycan chains in proteoglycans including chondroitin sulfate, heparan sulfate, heparin and dermatan sulfate. The enzyme activity, which is increased in scleroderma patients, is a diagnostic marker for the determination of sclerotic activity in systemic sclerosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]
Gene Details
Gene Symbol: XYLT2
Gene Name: Xylosyltransferase 2
Chromosome: CHR17: 48423392-48438512
Locus: 17q21.33
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: XYLT2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: XYLT2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping