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Rabbit anti-Human KCNK9 Polyclonal Antibody

The antibody against KCNK9 was raised in rabbit using the Synthetic peptide of Human KCNK9 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-26494A

The antibody against KCNK9 was raised in rabbit using the Synthetic peptide of Human KCNK9 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-26494A ClonalityPolyclonal
Host SpeciesRabbitTarget NameKCNK9
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthetic peptide of Human KCNK9Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9NPC2
Background Information
  • Uniprot Id

    Q9NPC2

  • Target Species

    Human

  • Target Name

    KCNK9

  • Target Full Name

    Potassium channel subfamily K member 9

  • Target Function

    pH-dependent, voltage-insensitive, background potassium channel protein.

  • Target Involvement

    Birk-Barel mental retardation dysmorphism syndrome (BIBAS)

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    Two pore domain potassium channel (TC 1.A.1.8) family

  • Target Tissue Specificity

    Mainly found in the cerebellum. Also found in adrenal gland, kidney and lung.

  • Target Synonyms

    KCNK9; TASK3; Potassium channel subfamily K member 9; Acid-sensitive potassium channel protein TASK-3; TWIK-related acid-sensitive K(+ channel 3; Two pore potassium channel KT3.2; Two pore K(+ channel KT3.2

  • Target Background

    This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH-dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel dysmorphism syndrome. Alternative splicing results in multiple transcript variants.

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