AFF2 Antibody
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货号:CSB-PA001413LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) AFF2 Polyclonal antibody
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Uniprot No.:P51816
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基因名:AFF2
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别名: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
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human AF4/FMR2 family member 2 protein (575-705AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,AFF2 Antibody (CSB-PA001413LA01HU),的标记方式是Non-conjugated。对于AFF2 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
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靶点详情
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功能:RNA-binding protein. Might be involved in alternative splicing regulation through an interaction with G-quartet RNA structure.
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基因功能参考文献:
- 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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相关疾病:Mental retardation, X-linked, associated with fragile site FRAXE (MRFRAXE)
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亚细胞定位:Nucleus speckle. Note=When splicing is inhibited, accumulates in enlarged speckles.
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蛋白家族:AF4 family
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组织特异性:Brain (most abundant in hippocampus and amygdala), placenta and lung.
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数据库链接:
HGNC: 3776
OMIM: 300806
KEGG: hsa:2334
STRING: 9606.ENSP00000359489
UniGene: Hs.496911
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