DAG1 polyclonal antibody-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
DAG1 polyclonal antibody

DAG1 polyclonal antibody

商家询价

产品名称: DAG1 polyclonal antibody

英文名称: DAG1 polyclonal antibody

产品编号: PAB18550

产品价格: null

产品产地: 台湾

品牌商标: Abnova

更新时间: null

使用范围:

亚诺法生技股份有限公司(Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152 点击查看
  • 传真 : 点击查看
  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of DAG1.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids at internal region of human DAG1.
  • Sequence:
  • C-HVGKHEYFMHATDK
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 100
  • Reactivity:
  • Human
  • Specificity:
  • Reported variants represent identical protein: NP_001159400.1, NP_004384.3.
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Storage Buffer:
  • In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Recommend Usage:
  • ELISA (1:128000)
    Western Blot (0.2-0.6 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • DAG1 polyclonal antibody (Cat # PAB18550) (0.2 ug/mL) staining of human skeletal muscle lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 1605
  • Gene Name:
  • DAG1
  • Gene Alias:
  • 156DAG,A3a,AGRNR,DAG
  • Gene Description:
  • dystroglycan 1 (dystrophin-associated glycoprotein 1)
  • Gene Summary:
  • Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants
  • Other Designations:
  • alpha-dystroglycan,beta-dystroglycan,dystroglycan 1,dystrophin-associated glycoprotein-1

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