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    FAM76A蛋白抗體
    • 產品貨號:
      BN41397R
    • 中文名稱:
      FAM76A蛋白抗體
    • 英文名稱:
      Rabbit anti-FAM76A Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN41397R-100ul

      100ul

      ¥2360.00

      交叉反應:Human,Mouse,Rat(predicted:Dog,Pig,Horse,Rabbit,Zebrafish) 推薦應用:WB,IHC-P,IHC-F,ICC,IF,ELISA

    • BN41397R-200ul

      200ul

      ¥3490.00

      交叉反應:Human,Mouse,Rat(predicted:Dog,Pig,Horse,Rabbit,Zebrafish) 推薦應用:WB,IHC-P,IHC-F,ICC,IF,ELISA

    產品描述

    英文名稱FAM76A
    中文名稱FAM76A蛋白抗體
    別    名Family with sequence similarity 76, member A; FLJ41946; Hypothetical protein LOC230789; MGC11672; RGD1305162; RP23-464L12.5; MGC34648; RP3-426I6.1; FA76A_HUMAN.  
    研究領域腫瘤  細胞生物  神經生物學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Human, Mouse, Rat,  (predicted: Dog, Pig, Horse, Rabbit, Zebrafish, )
    產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量35kDa
    細胞定位細胞核 細胞漿 細胞外基質 分泌型蛋白 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human FAM76A:151-250/307 
    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Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產品介紹Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM76A gene product has been provisionally designated FAM76A pending further characterization.

    Similarity:
    Belongs to the FAM76 family.

    SWISS:
    Q8TAV0

    Gene ID:
    199870

    Database links:

    Entrez Gene: 199870 Human

    Entrez Gene: 230789 Mouse

    Entrez Gene: 362618 Rat

    SwissProt: Q8TAV0 Human

    SwissProt: Q922G2 Mouse



    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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