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    • SLC26A4 Polyclonal Antibody

    SLC26A4 Polyclonal Antibody

    PA5115911
    Antibody detects endogenous levels of total SLC26A4. Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene.
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    CAT NUM
    PRODUCT NAME
    Pack Size
    PRICE
    QUANTITY
     
    CAT NUM: PA5115911
    SLC26A4 Polyclonal Antibody
    Pack Size: 100 μL
    PRICE: 

    Antigen
    SLC26A4
    Applications
    Immunocytochemistry
    Classification
    Polyclonal
    Concentration
    1 mg/mL
    Conjugate
    Unconjugated
    Form
    Liquid
    Formulation
    PBS with 50% glycerol and 0.02% sodium azide
    Gene
    SLC26A4
    Gene Alias
    DFNB4; EVA; PDS; Pendred syndrome homolog; Pendred's syndrome; pendrin; Slc26a4; Sodium-independent chloride/iodide transporter; solute carrier family
    Gene Accession No
    O43511, Q9R154, Q9R155
    Gene ID Entrez
    23985, 29440, 5172
    Gene Symbols
    SLC26A4
    Host Species
    Rabbit
    Immunogen
    A synthesized peptide derived from human SLC26A4(Accession O43511), corresponding to amino acid residues L498-L548.
    Isotype
    IgG
    Primary or Secondary
    Primary
    Product Type
    Antibody
    Purification Method
    Affinity chromatography
    Regulatory Status
    RUO
    Content And Storage
    -20°C
    Target Species
    Human
    Brand
    Invitrogen
    Pack Size
    100 μL
    Storage Temp
    Freezer (-5 to -30 C)
    Category
    Primary Antibodies

    Antibody detects endogenous levels of total SLC26A4. Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene.
    CONTACT US

    Rhenium Ltd
    Tel: +972-8-955-8888
    E-mail:  [email protected] 
     Hasatat 20, P.O.B 180, Modi’in 7171101, Israel
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