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      Rabbit Anti-gamma Sarcoglycan/Cy5.5 Conjugated antibody (bs-16231R-Cy5.5)
      訂購熱線:400-901-9800
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      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-16231R-Cy5.5
      英文名稱 Rabbit Anti-gamma Sarcoglycan/Cy5.5 Conjugated antibody
      中文名稱 Cy5.5標記的γ-肌聚糖/肌聚糖​​伽瑪/γ-sarcoglycan抗體
      別    名 35 kDa dystrophin associated glycoprotein; 35 kDa dystrophin-associated glycoprotein; 35DAG; 35kD dystrophin associated glycoprotein; 35kDa dystrophin-associated glycoprotein; A4; DAGA4; DMDA; DMDA1; Gamma SG; Gamma-sarcoglycan; Gamma-SG; LGMD2C; MAM; MGC130048; Sarcoglycan gamma; SCARMD2; SCG3; SGCG; SGCG_HUMAN; TYPE.  
      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  免疫學  信號轉導  細胞骨架  跨膜蛋白  
      抗體來源 Rabbit
      克隆類型 Polyclonal
      交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Sheep, )
      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 32kDa
      性    狀 Lyophilized or Liquid
      濃    度 1mg/ml
      免 疫 原 KLH conjugated synthetic peptide derived from human gamma Sarcoglycan
      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 °C 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°C. 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 °C.
      產品介紹 background:
      This gene encodes gamma-sarcoglycan, one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin. The dystrophin-glycoprotein complex (DGC) spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C). [provided by RefSeq, Oct 2008]

      Function:
      Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix.

      Subunit:
      Interacts with the syntrophin SNTA1. Cross-link to form 2 major subcomplexes: one consisting of SGCB, SGCD and SGCG and the other consisting of SGCB and SGCD. The association between SGCB and SGCG is particularly strong while SGCA is loosely associated with the other sarcoglycans (By similarity). Interacts with FLNC.

      Subcellular Location:
      Cell membrane; sarcolemma. Cytoplasm > cytoskeleton.

      Tissue Specificity:
      Expressed in skeletal and heart muscle.

      DISEASE:
      Defects in SGCG are the cause of limb-girdle muscular dystrophy type 2C (LGMD2C) [MIM:253700]. LGMD2C is characterized by progressive muscle wasting from early childhood.

      Similarity:
      Belongs to the sarcoglycan beta/delta/gamma/zeta family.

      Database links:

      Entrez Gene: 6445 Human

      Omim: 608896 Human

      SwissProt: Q13326 Human

      Unigene: 37167 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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