FMR1 Mutant (I304N) Human Recombinant Protein
Product Specifications
Background
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]
Overview
Purified mutant recombinant protein of Human fragile X mental retardation 1 (FMR1), transcript variant ISO1, mutation at (I304N)
Synonyms
FMRP; FRAXA; POF; POF1; POFX
Gene ID
2332
Accession Number mRNA
NM_002024
Chromosomal Location
Xq27.3
Expression System
HEK293
Tag
Myc-DDK
Concentration
>50 ug/mL as determined by microplate Bradford method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
71 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
FMR1
Species
Human
Protein ID
NP_002015.1
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/2332
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_002024
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_002015.1
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