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Last updated: 2017/8/13

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SNTG2 polyclonal antibody

  • Catalog # : PAB6578
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of SNTG2.
  • Immunogen:
  • A synthetic peptide corresponding to human SNTG2.
  • Sequence:
  • C-DSQSLARKYMYSS
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 60.2
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:8000)
    Western Blot (1 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • SNTG2 polyclonal antibody (Cat # PAB6578, 0.3 ug/mL) staining of human duodenum 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
  • Gene Name:
  • SNTG2
  • Gene Alias:
  • G2SYN,MGC133174,SYN5
  • Gene Description:
  • syntrophin, gamma 2
  • Gene Summary:
  • This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq
  • Other Designations:
  • gamma2-syntrophin,syntrophin 5
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