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Rabbit anti-Human CLN8 Polyclonal Antibody

The antibody against CLN8 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 200-286 of human CLN8 (NP_061764.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

ADA-03907A

The antibody against CLN8 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 200-286 of human CLN8 (NP_061764.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

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Specifications


Cat.No ADA-03907A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCLN8
Target SynonymsEPMR; TLCD6; C8orf61; CLN8FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, K-562, LO2, SKOV3ApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 200-286 of human CLN8 (NP_061764.2).Target SpeciesHuman
Immunogen SequenceMFHCRMVLTYHMWWVCFWHWDGLVSSLYLPHLTLFLVGLALLTLIINPYWTHKKTQQLLNPVDWNFAQPEAKSRPEGNGQLLRKKRPUniprot IDQ9UBY8
Background Information
  • Uniprot Id

    Q9UBY8

  • Target Species

    Human

  • Target Name

    CLN8

  • Target Full Name

    Protein CLN8

  • Target Function

    Could play a role in cell proliferation during neuronal differentiation and in protection against cell death.

  • Target Involvement

    Ceroid lipofuscinosis, neuronal, 8 (CLN8); Ceroid lipofuscinosis, neuronal, 8, Northern epilepsy variant (CLN8NE)

  • Target Subcellular Location

    Endoplasmic reticulum membrane; Multi-pass membrane protein. Endoplasmic reticulum-Golgi intermediate compartment membrane; Multi-pass membrane protein. Endoplasmic reticulum.

  • Target Synonyms

    CLN8; C8orf61; Protein CLN8

  • Target Background

    This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain.

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