Western Blot
Positive WB detected in: A549 whole cell lysate
All lanes: AFF2 antibody at 5µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 145, 141, 48, 144, 106 kDa
Observed band size: 145 kDa
AF4/FMR2 family member 2 antibody; AF4/FMR2 family, member 2 antibody; AFF2 antibody; AFF2_HUMAN antibody; FMR2 antibody; FMR2P antibody; Fragile X E mental retardation syndrome protein antibody; fragile X mental retardation 2 antibody; Fragile X mental retardation 2 protein antibody; fragile X mental retardation gene associated with FRAXE antibody; FRAXE antibody; mild or borderline mental retardation antibody; MRX2 antibody; OTTHUMP00000024204 antibody; OX19 antibody; Protein FMR-2 antibody; Protein Ox19 antibody
宿主:
Rabbit
反應種屬:
Human
免疫原:
Recombinant Human AF4/FMR2 family member 2 protein (575-705AA)
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期:
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途:
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
RNA-binding protein. Might be involved in alternative splicing regulation through an interaction with G-quartet RNA structure.
基因功能參考文獻:
Partial AFF2 microduplication in a patient with auditory processing disorder, emotional impairment and macrosomia. PMID: 25256661
FMR2 is an upstream regulator of FOS and JUN, and further link deregulation of the immediate early response genes to the pathology of ID- and FRAXE-associated ID in particular. PMID: 23562910
2.5% of males Autism spectrum disorder patients had missense mutations in AFF2 at highly conserved evolutionary sites. PMID: 22773736
A report of novel deletions involving AFF2 provide evidence for a new mutational spectrum, microdeletions, that are responsible for Fragile X E in a small subset of patients. PMID: 22065534
overexpression of AFF2/3/4 interferes with the organization and/or biogenesis of nuclear speckles. PMID: 21330300
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相關疾病:
Mental retardation, X-linked, associated with fragile site FRAXE (MRFRAXE)
亞細胞定位:
Nucleus speckle. Note=When splicing is inhibited, accumulates in enlarged speckles.
蛋白家族:
AF4 family
組織特異性:
Brain (most abundant in hippocampus and amygdala), placenta and lung.