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Rabbit anti-Human TMC1 Polyclonal Antibody

The antibody against TMC1 was raised in rabbit using the Human TMC1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

ADC-46916A

The antibody against TMC1 was raised in rabbit using the Human TMC1 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-46916A ClonalityPolyclonal
Host SpeciesRabbitTarget NameTMC1
Target SynonymsTMC1; Transmembrane channel-like protein 1; Transmembrane cochlear-expressed protein 1FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azidePurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman TMC1Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ8TDI8
Background Information
  • Uniprot Id

    Q8TDI8

  • Target Species

    Human

  • Target Name

    TMC1

  • Target Full Name

    Transmembrane channel-like protein 1

  • Target Function

    Probable ion channel required for the normal function of cochlear hair cells.

  • Target Involvement

    Deafness, autosomal dominant, 36 (DFNA36); Deafness, autosomal recessive, 7 (DFNB7)

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    TMC family

  • Target Tissue Specificity

    Detected in fetal cochlea, and at low levels in placenta and testis.

  • Target Synonyms

    TMC1; Transmembrane channel-like protein 1; Transmembrane cochlear-expressed protein 1

  • Target Background

    This gene is considered a member of a gene family predicted to encode transmembrane proteins. The specific function of this gene is unknown; however, it is known to be required for normal function of cochlear hair cells. Mutations in this gene have been associated with progressive postlingual hearing loss and profound prelingual deafness.

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