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Rabbit anti-Human CLN6 Polyclonal Antibody

The antibody against CLN6 was raised in rabbit using the Synthesized peptide derived from internal of Human CLN6. as the immunogen. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This antibody has been validated on ELISA, WB, IHC.

ADC-41336A

The antibody against CLN6 was raised in rabbit using the Synthesized peptide derived from internal of Human CLN6. as the immunogen. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This antibody has been validated on ELISA, WB, IHC.

$297.00

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Specifications


Cat.No ADC-41336A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCLN6
Target SynonymsCLN6; Ceroid-lipofuscinosis neuronal protein 6; Protein CLN6FormLiquid
Species ReactivityHumanStorage BufferPH 7.4, 0.02% sodium azide and 50% glycerol., 150mM NaCl, Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+)
Purification MethodThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.ApplicationELISA, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthesized peptide derived from internal of Human CLN6.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9NWW5
Background Information
  • Uniprot Id

    Q9NWW5

  • Target Species

    Human

  • Target Name

    CLN6

  • Target Full Name

    Ceroid-lipofuscinosis neuronal protein 6

  • Target Involvement

    Ceroid lipofuscinosis, neuronal, 6 (CLN6); Ceroid lipofuscinosis, neuronal, 4A (CLN4A)

  • Target Subcellular Location

    Endoplasmic reticulum membrane; Multi-pass membrane protein. Endoplasmic reticulum.

  • Target Synonyms

    CLN6; Ceroid-lipofuscinosis neuronal protein 6; Protein CLN6

  • Target Background

    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.

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