FMR1 FISH Probe
Our FMR1 probe is designed to detect FMR1 amplifications and deletions. The probe comes labeled in orange, but can 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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| FMR1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |
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| FMR1-20-RE | 20 (40 μL) | 200 μL |
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| FMR1-20-AQ | 20 (40 μL) | 200 μL |
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| FMR1-20-GR | 20 (40 μL) | 200 μL |
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| FMR1-20-GO | 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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