SLC26A5 polyclonal antibody

Catalog # PAB11608

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Size:100 ug
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of SLC26A5.

    Immunogen

    A synthetic peptide corresponding to human SLC26A5.

    Sequence

    ERLHTKDKVPDSIAD-C

    Host

    Goat

    Theoretical MW (kDa)

    81.3, 74.8, 56.5, 36

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Quality Control Testing

    Antibody Reactive Against Synthetic Peptide.

    Recommend Usage

    ELISA (1:32000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — SLC26A5

    Entrez GeneID

    375611

    Protein Accession#

    NP_945350.1;NP_996766.1;NP_996767.1;NP_996768.1

    Gene Name

    SLC26A5

    Gene Alias

    DFNB61, MGC118886, MGC118887, MGC118888, MGC118889, PRES

    Gene Description

    solute carrier family 26, member 5 (prestin)

    Omim ID

    604943

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the SLC26A/SulP transporter family. It encodes a protein that is specifically expressed in outer hair cells (OHCs) of the cochlea and is essential in auditory processing. Intracellular anions are thought to act as extrinsic voltage sensors, which bind to this protein and trigger the conformational changes required for rapid length changes in OHCs. Mutations in this gene have been associated with non-syndromic hearing loss. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq

    Other Designations

    OTTHUMP00000195086|deafness, neurosensory, autosomal recessive, 61|prestin|prestin (motor protein)

  • Disease
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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