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    C9orf115 Rabbit pAb (bs-15309R)  
    訂購熱線(xiàn):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-15309R
    英文名稱(chēng) C9orf115 Rabbit pAb
    中文名稱(chēng) 9號染色體開(kāi)放閱讀框115抗體
    別    名 MGC51999; Peptidyl tRNA hydrolase 1 homolog; PTH; PTH1; PTRH1 peptidyl tRNA hydrolase 1 homolog(S. cerevisiae); PTH_HUMAN.  
    研究領(lǐng)域 細胞生物  免疫學(xué)  染色質(zhì)和核信號  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 Rat (predicted: Human,Mouse,Pig,Sheep,Cow,Horse)
    產(chǎn)品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/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 23 kDa
    檢測分子量
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human C9orf115: 101-200/214 
    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 PTRH1 is a 214 amino acid protein that belongs to the PTH family. The PTRH1 protein is believed to be involved in RNA splicing, silencing and metabolism. The PTRH1 gene is conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, A.thaliana and rice, and maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    Similarity:
    Belongs to the PTH family.

    SWISS:
    Q86Y79

    Gene ID:
    138428

    Database links:

    Entrez Gene: 138428 Human

    SwissProt: Q86Y79 Human



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