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Rabbit anti-Human RTN1 Polyclonal Antibody

The antibody against RTN1 was raised in rabbit using the Human RTN1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

ADC-51986A

The antibody against RTN1 was raised in rabbit using the Human RTN1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

$600.00

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Specifications


Cat.No ADC-51986A ClonalityPolyclonal
Host SpeciesRabbitTarget NameRTN1
Target SynonymsRTN1; NSP; Reticulon-1; Neuroendocrine-specific proteinFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium AzidePurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman RTN1Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ16799
Background Information
  • Uniprot Id

    Q16799

  • Target Species

    Human

  • Target Name

    RTN1

  • Target Full Name

    Reticulon-1

  • Target Function

    Inhibits amyloid precursor protein processing, probably by blocking BACE1 activity.

  • Target Subcellular Location

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

  • Target Tissue Specificity

    Expressed in neural and neuroendocrine tissues and cell cultures derived therefrom. Expression of isoform RTN1-C is strongly correlated with neuronal differentiation.

  • Target Synonyms

    RTN1; NSP; Reticulon-1; Neuroendocrine-specific protein

  • Target Background

    This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. This gene is considered to be a specific marker for neurological diseases and cancer, and is a potential molecular target for therapy. Alternative splicing results in multiple transcript variants.

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