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Last updated: 2017/8/13

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CLCN7 Pre-design Chimera RNAi

  • Catalog # : H00001186-R01
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Homo sapiens chloride channel 7 (CLCN7), mRNA.
  • Reactivity:
  • Human
  • Supplied Product:
  • DEPC water
  • Target Refseq:
  • NM_001287
  • Storage Instruction:
  • Store at -20°C, do not exceed 4 - 5 freeze-thaw cycles to ensure product integrity.
  • Note:
  • Position of the Chimera RNAi.

  • Publication Reference
  • Applications
  • RNAi Knockdown
  • Application Image
  • RNAi Knockdown
  • Gene Information
  • Entrez GeneID:
  • 1186
  • Gene Name:
  • CLCN7
  • Gene Alias:
  • CLC-7,CLC7,FLJ26686,FLJ39644,FLJ46423,OPTA2,OPTB4
  • Gene Description:
  • chloride channel 7
  • Gene Summary:
  • The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq
  • Other Designations:
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