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FLNB antibody

FLNB Reactivity: Human, Mouse, Rat IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7260435
  • Target See all FLNB Antibodies
    FLNB (Filamin B, beta (FLNB))
    Reactivity
    • 43
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 38
    • 4
    • 1
    Rabbit
    Clonality
    • 40
    • 3
    Polyclonal
    Conjugate
    • 26
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FLNB antibody is un-conjugated
    Application
    • 41
    • 13
    • 13
    • 10
    • 9
    • 8
    • 8
    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human FLNB (NP_001157789.1).
    Isotype
    IgG
  • Application Notes
    IHC 1:50-1:100 IF 1:20-1:100
    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
    FLNB (Filamin B, beta (FLNB))
    Alternative Name
    FLNB (FLNB Products)
    Synonyms
    ABP-278 antibody, ABP-280 antibody, AOI antibody, FH1 antibody, FLN-B antibody, FLN1L antibody, LRS1 antibody, SCT antibody, TABP antibody, TAP antibody, AL024016 antibody, filamin B antibody, filamin, beta antibody, FLNB antibody, Flnb antibody
    Background
    This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3, boomerang dysplasia, autosomal dominant Larsen syndrome, and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.
    Gene ID
    2317
    UniProt
    O75369
    Pathways
    Maintenance of Protein Location
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