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    ZNF827 Rabbit pAb (bs-16441R)  
    訂購熱線(xiàn):400-901-9800
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    訂購QQ:  400-901-9800
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    50ul/1180.00元
    100ul/1980.00元
    200ul/2800.00元
    大包裝/詢(xún)價(jià)
    產(chǎn)品編號 bs-16441R
    英文名稱(chēng) ZNF827 Rabbit pAb
    中文名稱(chēng) 鋅指蛋白827抗體
    別    名 Zfp827; Zinc finger protein 827; ZN827_HUMAN; ZNF827.  
    研究領(lǐng)域 轉錄調節因子  鋅指蛋白  表觀(guān)遺傳學(xué)  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Chicken,Dog)
    產(chǎn)品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 119 kDa
    檢測分子量
    細胞定位 細胞核 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human ZNF827: 1-100/1081 
    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 ZNF827 (zinc finger protein 827) is a 1,081 amino acid nuclear protein that contains nine C2H2-type zinc fingers and belongs to the krueppel C2H2-type zinc-finger protein family. Existing as three alternatively spliced isoforms, ZNF827 may be involved in transcriptional regulation. The gene that encodes ZNF827 consists of around 181,000 bases and maps to human chromosome 4q31.2. Chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is encoded by a gene that maps to chromosome 4. FGFR-3 is also encoded by a gene located on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

    Function:
    May be involved in transcriptional regulation.

    Subcellular Location:
    Nucleus.

    Similarity:
    Belongs to the krueppel C2H2-type zinc-finger protein family.
    Contains 9 C2H2-type zinc fingers.

    SWISS:
    Q17R98

    Gene ID:
    152485

    Database links:

    Entrez Gene: 152485 Human

    Entrez Gene: 622675 Mouse

    SwissProt: Q17R98 Human

    SwissProt: Q505G8 Mouse

    Unigene: 133916 Human

    Unigene: 48724 Mouse



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