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CLN5 (Human) Recombinant Protein (P01)

  • Catalog # : H00001203-P01
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Human CLN5 full-length ORF (BAG52069.1, 1 a.a. - 358 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • MAQEVDTAQGAEMRRGAGAARGRASWCWALALLWLAVVPGWSRVSGIPSRRHWPVPCKRFDFRPKPDPYCQAKYTFCPTGSPIPVMEGDDDTEVFRLQAPVWEFKYGDLLGHLKIMHDAIGFRSTLTGKNYTMEWYELFQLGNCTFPHLRPEMDAPFWCNQGAACFFEGIDDVHWKENGTLVQVATISGNMFNQMAKWVKQDNETGIYYETWNVKASPEKGAETWFDSYDCSKFVLRTFNKLAEFGAEFKNIETNYTRIFLYSGEPTYLGNETSVFGPTGNKTLGLAIKRFYYPFKPHLPTKEFLLSLLQIFDAVIVHKQFYLFYNFEYWFLPMKFPFIKITYEEIPLPIRNKTLSGL
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 67.8
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 1203
  • Gene Name:
  • CLN5
  • Gene Alias:
  • FLJ90628,NCL
  • Gene Description:
  • ceroid-lipofuscinosis, neuronal 5
  • Gene Summary:
  • This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function
  • Other Designations:
  • OTTHUMP00000018521
  • Gene Pathway
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