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Rabbit anti-Human STX16 Polyclonal Antibody

The antibody against STX16 was raised in rabbit using the Fusion protein of Human STX16 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-29186A

The antibody against STX16 was raised in rabbit using the Fusion protein of Human STX16 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$299.00

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Specifications


Cat.No ADC-29186A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSTX16
Target SynonymsSTX16; Syntaxin-16; Syn16FormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBSPurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionFusion protein of Human STX16Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDO14662
Background Information
  • Uniprot Id

    O14662

  • Target Species

    Human

  • Target Name

    STX16

  • Target Full Name

    Syntaxin-16

  • Target Function

    SNARE involved in vesicular transport from the late endosomes to the trans-Golgi network.

  • Target Involvement

    Pseudohypoparathyroidism 1B (PHP1B)

  • Target Subcellular Location

    Golgi apparatus membrane; Single-pass type IV membrane protein.; [Isoform C]: Cytoplasm.

  • Target Protein Families

    Syntaxin family

  • Target Tissue Specificity

    Ubiquitous.

  • Target Synonyms

    STX16; Syntaxin-16; Syn16

  • Target Background

    This gene encodes a protein that is a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V-SNARES (vesicle-SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this gene. Read-through transcription also exists between this gene and the neighboring downstream aminopeptidase-like 1 (NPEPL1) gene.

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