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    APBB3 Rabbit pAb (bs-11637R)  
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    產(chǎn)品編號 bs-11637R
    英文名稱(chēng) APBB3 Rabbit pAb
    中文名稱(chēng) 鐵蛋白Fe65樣蛋白2抗體
    別    名 FE65L2; Amyloid beta A4 precursor protein binding family B member 3; Amyloid beta A4 precursor protein-binding family B member 3; amyloid beta precursor protein binding family B member 3; amyloid precursor interacting protein; Apbb3; APBB3_HUMAN; Fe65 like protein 2; FE65L2; Protein Fe65-like 2; SRA.  
    研究領(lǐng)域 細胞生物  神經(jīng)生物學(xué)  信號轉導  Alzheimer's  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 Mouse,Rat (predicted: Human,Sheep,Cow,Dog)
    產(chǎn)品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 52 kDa
    檢測分子量
    細胞定位 細胞核 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human APBB3: 401-486/486 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產(chǎn)品介紹 Fe65L2 is a 486 amino acid protein that contains one WW domain and two PID domains. Binding to the intracellular domain of the ∫-Amyloid precursor protein, Fe65L2 is thought to modulate the internalization and, therefore, the accessibility and function of ∫-Amyloid. Via its ability to control the intracellular accumulation of ∫-Amyloid, Fe65L2 is thought to play a role in the pathogenesis of Alzheimer's disease. Fe65L2 exists as four alternatively spliced isoforms designated isoform I, isoform II, isoform III and isoform IV. Fe65L2 interacts with Amyloid-like protein and is encoded by a gene located on human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    Function:
    May modulate the internalization of beta-amyloid precursor protein.

    Subunit:
    Binds to the intracellular domain of the beta-amyloid precursor protein. Also binds to APP-like proteins.

    Tissue Specificity:
    Expressed in various tissues.

    Similarity:
    Contains 2 PID domains.
    Contains 1 WW domain.

    SWISS:
    O95704

    Gene ID:
    10307

    Database links:

    Entrez Gene: 10307 Human

    Entrez Gene: 225372 Mouse

    Entrez Gene: 117026 Rat

    Omim: 602711 Human

    SwissProt: O95704 Human

    SwissProt: Q8R1C9 Mouse

    SwissProt: O35827 Rat

    Unigene: 529449 Human

    Unigene: 89673 Mouse

    Unigene: 30067 Rat



    產(chǎn)品圖片
    Sample: Cerebrum (Mouse) Lysate at 40 ug Primary: Anti- APBB3 (bs-11637R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 52 kD Observed band size: 52 kD
    Paraformaldehyde-fixed, paraffin embedded (Rat brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (APBB3) Polyclonal Antibody, Unconjugated (bs-11637R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructions and DAB staining.
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