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    2. 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>>半胱氨酸亞磺酸脫羧酶抗體
      半胱氨酸亞磺酸脫羧酶抗體
      • 產品貨號:
        BN40330R
      • 中文名稱:
        半胱氨酸亞磺酸脫羧酶抗體
      • 英文名稱:
        Rabbit anti-CSAD Polyclonal antibody
      • 品牌:
        Biorigin
      • 貨號

        產品規格

        售價

        備注

      • BN40330R-100ul

        100ul

        ¥2360.00

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

      • BN40330R-200ul

        200ul

        ¥3490.00

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

      產品描述

      英文名稱CSAD
      中文名稱半胱氨酸亞磺酸脫羧酶抗體
      別    名CSAD; CSAD_HUMAN; CSD; Cysteine sulfinic acid decarboxylase; Cysteine-sulfinate decarboxylase; Sulfinoalanine decarboxylase.  
      研究領域腫瘤  神經生物學  信號轉導  新陳代謝  
      抗體來源Rabbit
      克隆類型Polyclonal
      交叉反應Mouse, Rat,  (predicted: Human, Dog, 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55kDa
      細胞定位細胞漿 細胞外基質 
      性    狀Liquid
      濃    度1mg/ml
      免 疫 原KLH conjugated synthetic peptide derived from human CSAD:401-493/493 
      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CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

      Subunit:
      Homodimer.

      Similarity:
      Belongs to the group II decarboxylase family.

      SWISS:
      Q9Y600

      Gene ID:
      51380

      Database links:
      UniProtKB/Swiss-Prot: Q9Y600.2

      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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