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Rabbit anti-Human VPS16 Polyclonal Antibody

The antibody against VPS16 was raised in rabbit using the Fusion protein of Human VPS16 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-28951A

The antibody against VPS16 was raised in rabbit using the Fusion protein of Human VPS16 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-28951A ClonalityPolyclonal
Host SpeciesRabbitTarget NameVPS16
FormLiquidSpecies ReactivityHuman, Mouse
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionFusion protein of Human VPS16Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9H269
Background Information
  • Uniprot Id

    Q9H269

  • Target Species

    Human

  • Target Name

    VPS16

  • Target Full Name

    Vacuolar protein sorting-associated protein 16 homolog

  • Target Function

    Plays a role in vesicle-mediated protein trafficking to lysosomal compartments including the endocytic membrane transport and autophagic pathways. Believed to act as a core component of the putative HOPS and CORVET endosomal tethering complexes which are proposed to be involved in the Rab5-to-Rab7 endosome conversion probably implicating MON1A/B, and via binding SNAREs and SNARE complexes to mediate tethering and docking events during SNARE-mediated membrane fusion. The HOPS complex is proposed to be recruited to Rab7 on the late endosomal membrane and to regulate late endocytic, phagocytic and autophagic traffic towards lysosomes. The CORVET complex is proposed to function as a Rab5 effector to mediate early endosome fusion probably in specific endosome subpopulations. Required for recruitment of VPS33A to the HOPS complex. Required for fusion of endosomes and autophagosomes with lysosomes; the function is dependent on its association with VPS33A but not VPS33B. The function in autophagosome-lysosome fusion implicates STX17 but not UVRAG.

  • Target Involvement

    VSP16 mutation have been found in one familly with adolescent-onset primary dystonia. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures.

  • Target Subcellular Location

    Late endosome membrane; Peripheral membrane protein; Cytoplasmic side. Lysosome membrane; Peripheral membrane protein; Cytoplasmic side. Early endosome. Cytoplasmic vesicle, clathrin-coated vesicle. Cytoplasmic vesicle, autophagosome.

  • Target Protein Families

    VPS16 family

  • Target Tissue Specificity

    Ubiquitous.

  • Target Synonyms

    HGNC:14584; hVPS16; mVPS16; RP11 12M19.2; Vacuolar protein sorting 16 (yeast); Vacuolar protein sorting 16 (Yeast); isoform CRA_a; Vacuolar protein sorting 16; Vacuolar protein sorting 16 homolog (S. cerevisiae); vacuolar protein sorting associated protein 16 homolog; Vacuolar protein sorting protein 16; Vacuolar protein sorting-associated protein 16 homolog; VPS16; VPS16_HUMAN; VPS16A

  • Target Background

    Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps16 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Two transcript variants encoding different isoforms have been found for this gene.

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