Specifications
Immunogen
FMR1 (NP_002015, 121 a.a. ~ 220 a.a) partial recombinant protein with GST tag. The sequence is ATKDTFHKIKLDVPEDLRQMCAKEAAHKDFKKAVGAFSVTYDPENYQLVILSINEVTSKR AHMLIDMHFRSLRTKLSLIMRNEEASKQLESSRQLASRFH
Target
Alternative Names
FMR1; fragile X mental retardation 1; POF; FMRP; POF1; FRAXA; fragile X mental retardation protein 1;
Product Background
Antigen Description
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.
Custom Antibody Labeling
We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody.
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Citations
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Hagerman, RJ; Hagerman, PJ; et al. Fragile X syndrome: A model of gene-brain-behaviour relationships. REVISTA DE NEUROLOGIA 33:S51-S57(2001).
Saffman, EE; Styhler, S; et al. Premature translation of oskar in oocytes lacking the RNA-binding protein bicaudal-C. MOLECULAR AND CELLULAR BIOLOGY 18:4855-4862(1998).