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Magic™ Membrane Protein Human CLN5 (CLN5 intracellular trafficking protein) Full Length (CAT#: MPC3593K) Made to Order

This product is a made-to-order Human CLN5 membrane protein expressed in HEK293. The protein is for research use only and is not approved for use in humans or in clinical diagnosis.

Product Specifications

  • Host Species
  • Human
  • Target Protein
  • CLN5
  • Protein Length
  • Full length
  • Protein Class
  • Receptor
  • TMD
  • 1
  • Sequence
  • MAQEVDTAQGAEMRRGAGAARGRASWCWALALLWLAVVPGWSRVSGIPSR
    RHWPVPYKRFDFRPKPDPYCQAKYTFCPTGSPIPVMEGDDDIEVFRLQAP
    VWEFKYGDLLGHLKIMHDAIGFRSTLTGKNYTMEWYELFQLGNCTFPHLR
    PEMDAPFWCNQGAACFFEGIDDVHWKENGTLVQVATISGNMFNQMAKWVK
    QDNETGIYYETWNVKASPEKGAETWFDSYDCSKFVLRTFNKLAEFGAEFK
    NIETNYTRIFLYSGEPTYLGNETSVFGPTGNKTLGLAIKRFYYPFKPHLP
    TKEFLLSLLQIFDAVIVHKQFYLFYNFEYWFLPMKFPFIKITYEEIPLPI
    RNKTLSGL

Product Description

  • Expression Systems
  • HEK293
  • Tag
  • Flag-StrepII or based on specific requirements
  • Protein Format
  • Detergent or based on specific requirements (Detergent, Liposome, Nanodisc, SMALPs, VLP)

Target

  • Target Protein
  • CLN5
  • Full Name
  • CLN5 intracellular trafficking protein
  • Introduction
  • 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.
  • Alternative Names
  • CLN5; ceroid-lipofuscinosis neuronal protein 5; ceroid-lipofuscinosis, neuronal 5; CLN5 intracellular trafficking protein

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