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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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