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    C3orf23 Rabbit pAb (bs-15169R)  
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    產(chǎn)品編號 bs-15169R
    英文名稱(chēng) C3orf23 Rabbit pAb
    中文名稱(chēng) 3號染色體開(kāi)放閱讀框23抗體
    別    名 C3orf23; TCAIM_HUMAN; Chromosome 3 open reading frame 23; D9Ertd402e; DKFZp313N0621; FLJ41686; Hypothetical protein LOC285343; MGC119530; MGC119531; MGC119532; MGC119533; TOAG1; Tolerance associated gene 1; Uncharacterized protein C3orf23.  
    研究領(lǐng)域 腫瘤  心血管  細胞生物  免疫學(xué)  發(fā)育生物學(xué)  線(xiàn)粒體  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 Human (predicted: Mouse,Rat,Rabbit)
    產(chǎn)品應用 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 58 kDa
    檢測分子量
    細胞定位 細胞漿 線(xiàn)粒體
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human C3orf23  
    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 C3orf23 (chromosome 3 open reading frame 23), also known as FLJ41686, MGC119530, MGC119531, MGC119532, MGC119533 or DKFZp313N062, is a 496 amino acid protein that exists as four alternatively spliced isoforms. C3orf23 is encoded by a gene mapping to human chromosome 3p21.33. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

    Function:
    May regulate T-cell apoptosis (By similarity).

    Subcellular Location:
    Mitochondrion (By similarity).

    SWISS:
    Q8N3R3

    Gene ID:
    285343

    Database links:

    Entrez Gene: 285343 Human

    SwissProt: Q8N3R3 Human

    SwissProt: Q66JZ4 Mouse

    Unigene: 55131 Human



    產(chǎn)品圖片
    Paraformaldehyde-fixed, paraffin embedded (human esophagus cancer); 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 (C3orf23) Polyclonal Antibody, Unconjugated (bs-15169R) at 1:500 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.
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