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Proteintech
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Immunogen sequence: MGGLASGGD VEPGLPVEVR GSNGAFYKGF VKDVHEDSVT IFFENNWQSE RQIPFGDVRL PPPADYNKEI TEGDEVEVYS RANEQEPCGW WLARVRMMKG DFYVIEYAAC DATYNEIVTL ERLRPVNPNP LATKGSFFKV TMAVPEDLRE ACSNENVHKE FKKALGANCI FLNITNSELF ILSTTEAPVK RASLLGDMHF RSLRTKLLLM SRNEEATKHL ETSKQLAAAF QEEFTVREDL MGLAIGTHGA NIQQARKVPG VTAIELGEET CTFRIYGETP EACRQARSYL EFSEDSVQVP RNLVGKVIGK NGKVIQEIVD KSGVVRVRVE GDNDKKNPRE EGMVPFIFVG TRENI (1-354 aa encoded by BC020090)
Fragile X syndrome is caused by the absence of the fragile X mental-retardation protein (FMRP). FMRP is the archetype of a class of cytoplasmic mRNA-binding proteins that includes the fragile X-related 1 and 2 proteins (FXR1 and FXR2). The fragile X-related proteins FXR1 and FXR2 contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: FMR1 autosomal homolog 2; fragile X mental retardation gene 2, autosomal homolog; fragile X mental retardation syndrome-related protein 2; fragile X mental retardation, autosomal homolog 2; fragile X mental retardation-related protein 2; fragile X-mental retardation 1-like 2; FXR2P; RNA-binding protein FXR2
Gene Aliases: FMR1L2; FXR2; Fxr2h; FXR2P
UniProt ID: (Human) P51116
Entrez Gene ID: (Human) 9513, (Mouse) 23879
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