AFF2 Break Apart FISH Probe
Empire Genomics’ AFF2 Break Apart FISH Probe is designed to flank the AFF2 gene and is typically used for detecting AFF2 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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| AFF2BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AFF2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| AFF2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| AFF2BA-20-GORE | 20 (40 μL) | 200 μL |
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| AFF2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| AFF2BA-20-GROR | 20 (40 μL) | 200 μL |
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| AFF2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| AFF2BA-20-REGO | 20 (40 μL) | 200 μL |
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| AFF2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a putative transcriptional activator that is a member of the AF4\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]
Gene Details
Gene Symbol: AFF2
Gene Name: AF4/FMR2 Family Member 2
Chromosome: CHRX: 147582138-148082193
Locus: Xq28
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: AFF2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: AFF2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping