Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

B9D1 antibody

B9D1 Reactivity: Human, Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264023
  • Target See all B9D1 Antibodies
    B9D1 (B9 Protein Domain 1 (B9D1))
    Reactivity
    • 9
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 8
    • 1
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 9
    This B9D1 antibody is un-conjugated
    Application
    • 9
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human B9D1 (NP_056496.1).
    Isotype
    IgG
    Top Product
    Discover our top product B9D1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    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
    This gene encodes 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. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17.
    Gene ID
    27077
    UniProt
    Q9UPM9
You are here:
Support