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RFX5 antibody (C-Term)

RFX5 Reactivity: Human WB, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7449604
  • Target See all RFX5 Antibodies
    RFX5 (Regulatory Factor X 5 (RFX5))
    Binding Specificity
    • 7
    • 7
    • 6
    • 6
    • 6
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    • 34
    • 5
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    Human
    Host
    • 31
    • 3
    • 1
    Rabbit
    Clonality
    • 33
    • 2
    Polyclonal
    Conjugate
    • 26
    • 2
    • 2
    • 2
    • 2
    • 2
    This RFX5 antibody is un-conjugated
    Application
    • 33
    • 20
    • 5
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    Rabbit anti-RFX5 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 575 and C-term
    Isotype
    IgG
    Top Product
    Discover our top product RFX5 Primary Antibody
  • Application Notes

    IP: 1 - 4 μg/mg lysate

    WB: 1:500 - 1:5,000

    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
    RFX5 (Regulatory Factor X 5 (RFX5))
    Alternative Name
    RFX5 (RFX5 Products)
    Synonyms
    regulatory factor X5 antibody, regulatory factor X, 5 (influences HLA class II expression) antibody, RFX5 antibody, Rfx5 antibody
    Background
    Background: Regulatory factor X-5 (RFX5) is a 75 kDa subunit of the regulatory factor X (RFX) heteromeric complex that activates the transcription of major histocompatibility class II (MHC-II) genes by binding MHC-II promoter elements. The RFX complex consists of RFX5, RFXANK, and RFXAP. Mutations in these genes result in a lack of MHCII transcription and lead to the severe combined immunodeficiency disease, Bare Lymphocyte Syndrome (BLS).
    Gene ID
    5993
    NCBI Accession
    NP_000440
    UniProt
    P48382
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