CG6 FISH Probe
The CG6 FISH probe is designed to hybridize to the CG6 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
---|---|---|---|---|
FMR1-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
FMR1-20-RE | 20 (40 μL) | 200 μL | ||
FMR1-20-GO | 20 (40 μL) | 200 μL | ||
FMR1-20-GR | 20 (40 μL) | 200 μL | ||
FMR1-20-AQ | 20 (40 μL) | 200 μL | ||
FMR1-20-DIG | 20 (40 μL) | 200 μL | ||
FMR1-20-BIO | 20 (40 μL) | 200 μL |
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: CG6 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