FMR1 Break Apart FISH Probe
Empire Genomics’ FMR1 Break Apart FISH Probe is designed to flank the FMR1 gene and is typically used for detecting FMR1 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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| FMR1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FMR1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| FMR1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FMR1BA-20-GORE | 20 (40 μL) | 200 μL |
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| FMR1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FMR1BA-20-GROR | 20 (40 μL) | 200 μL |
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| FMR1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FMR1BA-20-REGO | 20 (40 μL) | 200 μL |
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| FMR1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010]
Gene Details
Gene Symbol: FMR1
Gene Name: Fragile X Mental Retardation 1
Chromosome: CHRX: 146993468-147032647
Locus: Xq27.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FMR1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FMR1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping