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    Rabbit Anti-FAM134A/FITC Conjugated antibody (bs-14725R-FITC)
    訂購熱線:400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
    技術支持:techsupport@bioss.com.cn
    說 明 書: 100ul  
    100ul/2980.00元
    大包裝/詢價
    產品編號 bs-14725R-FITC
    英文名稱 Rabbit Anti-FAM134A/FITC Conjugated antibody
    中文名稱 FITC標記的FAM134A蛋白抗體
    別    名 C2orf17; F133B_HUMAN; FAM134A family with sequence similarity 134, member A.  
    規格價格 100ul/2980元 購買        大包裝/詢價
    說 明 書 100ul  
    研究領域 細胞生物  信號轉導  轉運蛋白  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    交叉反應 Human, 
    產品應用 ICC=1:50-200 IF=1:50-200 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 58kDa
    性    狀 Lyophilized or Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human FAM134A
    亞    型 IgG
    純化方法 affinity purified by Protein A
    儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件 Store at -20 癈 for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20癈. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 癈.
    產品介紹 background:
    The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM134A gene product has been provisionally designated FAM134A pending further characterization.

    Function:
    The function of this protein remains unknown.

    Subcellular Location:
    Membrane; Multipass membrane protein.

    Similarity:
    Belongs to the FAM133 family.

    Database links:

    Entrez Gene: 79137 Human

    Entrez Gene: 227298 Mouse

    Entrez Gene: 363252 Rat

    NCBI: NP_077269 Human

    SwissProt: Q8NC44 Human

    SwissProt: Q6NS82 Mouse

    SwissProt: Q3MHU5 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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