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ABHD11 antibody (AA 176-205)

ABHD11 Reactivity: Human WB, FACS Host: Rabbit Polyclonal RB24708 unconjugated
Catalog No. ABIN653369
  • Target See all ABHD11 Antibodies
    ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))
    Binding Specificity
    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 176-205
    Reactivity
    • 24
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 27
    • 2
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 13
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ABHD11 antibody is un-conjugated
    Application
    • 17
    • 16
    • 7
    • 2
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS)
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This ABHDB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 176-205 amino acids from the Central region of human ABHDB.
    Clone
    RB24708
    Isotype
    Ig Fraction
    Top Product
    Discover our top product ABHD11 Primary Antibody
  • Application Notes
    WB: 1:1000. FC: 1:10~50
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))
    Alternative Name
    ABHDB (ABHD11 Products)
    Background
    ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
    Molecular Weight
    34690
    Gene ID
    83451
    NCBI Accession
    NP_001138836, NP_683710, NP_683711
    UniProt
    Q8NFV4
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