FMR1 Monoclonal Antibody
Size: 50μL, 100μL
Catalogue Numbers: RA11234-50, RA11234-100
Citations, Manuals and MSDS Available upon request.
Background: fragile X mental retardation 1 (FMR1) Homo sapiens 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],
Condition: Ascitic fluid containing 0.03% sodium azide, 0.5% BSA, 50% glycerol.
Storage Instructions: -20°C/1 year
Applications: WB; IHC-p; IF/ICC; ELISA
Species Cross-Reactivity: Human
GeneID (Human): 2332
SWISS: Q06787
Source: Mouse
Research Use Only