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Fibrillin 1 antibody

FBN1 Reactivity: Human, Mouse IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2431320
  • Target See all Fibrillin 1 (FBN1) Antibodies
    Fibrillin 1 (FBN1)
    Reactivity
    • 58
    • 30
    • 21
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse
    Host
    • 69
    • 12
    • 1
    Rabbit
    Clonality
    • 71
    • 11
    Polyclonal
    Conjugate
    • 42
    • 16
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Fibrillin 1 antibody is un-conjugated
    Application
    • 56
    • 30
    • 30
    • 15
    • 14
    • 14
    • 13
    • 13
    • 12
    • 9
    • 5
    • 3
    • 2
    • 1
    Immunohistochemistry (IHC), ELISA
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human FBN1
    Isotype
    IgG
    Top Product
    Discover our top product FBN1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Fibrillin 1 (FBN1)
    Alternative Name
    FBN1 (FBN1 Products)
    Synonyms
    FBN1 antibody, ACMICD antibody, ECTOL1 antibody, FBN antibody, GPHYSD2 antibody, MASS antibody, MFS1 antibody, OCTD antibody, SGS antibody, SSKS antibody, WMS antibody, WMS2 antibody, AI536462 antibody, B430209H23 antibody, Fib-1 antibody, Tsk antibody, fibrillin 1 antibody, FBN1 antibody, Fbn1 antibody
    Background
    This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.
    NCBI Accession
    NP_000129
    Pathways
    Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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