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    最近搜索:細胞培養 微生物學 分子生物 生物化學
    首頁>>免疫學>>一抗>>甲硫氨酸轉運RNA合成酶2抗體
    甲硫氨酸轉運RNA合成酶2抗體
    • 產品貨號:
      BN40531R
    • 中文名稱:
      甲硫氨酸轉運RNA合成酶2抗體
    • 英文名稱:
      Rabbit anti-MARS2 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN40531R-100ul

      100ul

      ¥2360.00

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

    • BN40531R-200ul

      200ul

      ¥3490.00

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

    產品描述

    英文名稱MARS2
    中文名稱甲硫氨酸轉運RNA合成酶2抗體
    別    名mars2; Methionine tRNA ligase 2; Methionine tRNA ligase 2 mitochondrial; Methionine tRNA ligase; Methionine tRNA synthetase 2; Methionine--tRNA ligase; Methionyl tRNA synthetase 2 mitochondrial; Methionyl tRNA synthetase mitochondrial; Methionyl-tRNA synthetase 2; MetRS; mitochondrial; Mitochondrial methionine tRNA ligase; Mitochondrial methionyl tRNA synthetase; Mitochondrial methionyl-tRNA synthetase; MtMetRS; SYMM_HUMAN.  
    研究領域細胞生物  神經生物學  信號轉導  轉運蛋白  表觀遺傳學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Rat,  (predicted: Human, Mouse, Dog, Cow, Horse, )
    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63kDa
    細胞定位細胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human MARS2:31-130/593 
    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This gene produces a mitochondrial methionyl-tRNA synthetase protein that is encoded by the nuclear genome and imported to the mitochondrion. This protein likely functions as a monomer and is predicted to localize to the mitochondrial matrix. Mutations in this gene are associated with the autosomal recessive neurodegenerative disease spastic ataxia-3 (SPAX3). [provided by RefSeq, Apr 2014]

    DISEASE:
    Spastic ataxia 3, autosomal recessive (SPAX3) [MIM:611390]: A neurologic disorder characterized by cerebellar ataxia, ataxic gait, spasticity, and hyperreflexia. Other variable features include dysarthria, dysmetria, mild cognitive impairment, urinary urgency and dystonic positioning. Note: The disease is caused by mutations affecting the gene represented in this entry.

    Similarity:
    Belongs to the class-I aminoacyl-tRNA synthetase family.

    SWISS:
    Q96GW9

    Gene ID:
    92935

    Database links:

    Entrez Gene: 92935 Human

    Omim: 609728 Human

    SwissProt: Q96GW9 Human

    Unigene: 116602 Human

    Unigene: 744330 Human



    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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