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B9D1 antibody (C-Term)

B9D1 Reactivity: Human WB, IF, EIA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1450121
  • Target See all B9D1 Antibodies
    B9D1 (B9 Protein Domain 1 (B9D1))
    Binding Specificity
    • 3
    • 2
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    • 9
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 8
    • 1
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 9
    This B9D1 antibody is un-conjugated
    Application
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)
    Purification
    Affinity chromatography purified via peptide column
    Immunogen
    18 amino acid synthetic peptide near the carboxy terminus of Human B9D1
    Isotype
    IgG
    Top Product
    Discover our top product B9D1 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    1.0 mg/mL
    Buffer
    PBS containing 0.02 % Sodium Azide as preservative
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    B9D1 (B9 Protein Domain 1 (B9D1))
    Alternative Name
    B9D1 (B9D1 Products)
    Synonyms
    B9 antibody, EPPB9 antibody, MKS9 antibody, MKSR1 antibody, AW045994 antibody, Eppb9 antibody, im:6905750 antibody, im:7069491 antibody, wu:fc09g07 antibody, zgc:110733 antibody, B9 domain containing 1 antibody, B9 protein domain 1 antibody, B9D1 antibody, B9d1 antibody, b9d1 antibody
    Background
    Meckel syndrome (MKS) is an embryonic lethal, autosomal recessive disorder characterized by polycystic kidney disease, central nervous system defects, polydactyly and liver fibrosis. B9D1 is a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. B9D1, and its related protein B9D2, form a complex with MKS1, disruption of which causes MKS. B9D1 is thought to be required for normal hedgehog signaling, ciliogenesis, and ciliary protein localization .Synonyms: B9 domain-containing protein 1, EPPB9
    Gene ID
    27077
    NCBI Accession
    NP_056496
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