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SLC26A4 antibody (AA 250-350)

SLC26A4 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7270442
  • Target See all SLC26A4 Antibodies
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    Binding Specificity
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 250-350
    Reactivity
    • 12
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 9
    • 3
    Rabbit
    Clonality
    • 10
    • 2
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    This SLC26A4 antibody is un-conjugated
    Application
    • 9
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    SLC26A4 Rabbit pAb
    Sequence
    VLSIIYTLVE IFQNIGDTNL ADFTAGLLTI VVCMAVKELN DRFRHKIPVP IPIEVIVTII ATAISYGANL EKNYNAGIVK SIPRGFLPPE LPPVSLFSEM L
    Cross-Reactivity
    Mouse
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide corresponding to a sequence within amino acids 250-350 of human SLC26A4 (NP_000432.1).
    Isotype
    IgG
    Top Product
    Discover our top product SLC26A4 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    Alternative Name
    SLC26A4 (SLC26A4 Products)
    Synonyms
    Pds antibody, DFNB4 antibody, EVA antibody, PDS antibody, TDH2B antibody, pendrin antibody, solute carrier family 26 member 4 antibody, solute carrier family 26, member 4 antibody, SLC26A4 antibody, Slc26a4 antibody
    Background
    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; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.,SLC26A4;DFNB4;EVA;PDS;TDH2B;pendrin,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,SLC26A4
    Molecular Weight
    39kDa/85kDa
    Gene ID
    5172
    UniProt
    O43511
    Pathways
    Thyroid Hormone Synthesis, Sensory Perception of Sound
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