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

FXR2 antibody (AA 600-635)

FXR2 Reactivity: Human WB, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7450263
  • Target See all FXR2 Antibodies
    FXR2 (Fragile X Mental Retardation, Autosomal Homolog 2 (FXR2))
    Binding Specificity
    • 7
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 600-635
    Reactivity
    • 30
    • 20
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 25
    • 5
    Rabbit
    Clonality
    • 27
    • 3
    Polyclonal
    Conjugate
    • 23
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FXR2 antibody is un-conjugated
    Application
    • 22
    • 11
    • 7
    • 7
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    Rabbit anti-FXR2 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    Between AA 600 and 635
    Isotype
    IgG
    Top Product
    Discover our top product FXR2 Primary Antibody
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
    Expiry Date
    12 months
  • Target
    FXR2 (Fragile X Mental Retardation, Autosomal Homolog 2 (FXR2))
    Alternative Name
    FXR2 (FXR2 Products)
    Background
    Background: FXR2 is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. FXR2 may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X mental retardation syndrome [taken from NCBI Entrez Gene (Gene ID: 8087)].
    Gene ID
    9513
    NCBI Accession
    NP_004851
    UniProt
    P51116
You are here:
Chat with us!