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RBM17 antibody (AA 25-75)

This Rabbit Polyclonal antibody specifically detects RBM17 in WB, IP and IHC (fp). It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7453552

Quick Overview for RBM17 antibody (AA 25-75) (ABIN7453552)

Target

See all RBM17 Antibodies
RBM17 (RNA Binding Motif Protein 17 (RBM17))

Reactivity

  • 19
  • 6
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 18
  • 5
Rabbit

Clonality

  • 19
  • 4
Polyclonal

Conjugate

  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This RBM17 antibody is un-conjugated

Application

  • 12
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 2
    • 2
    • 2
    • 2
    AA 25-75

    Purpose

    Rabbit anti-SPF45 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 25 and 75

    Isotype

    IgG
  • Application Notes

    IHC: 1:1,000 - 1:5,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: Not recommended. Use rabbit anti-SPF45 antibody ABIN7453790.

    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

    RBM17 (RNA Binding Motif Protein 17 (RBM17))

    Alternative Name

    SPF45

    Background

    Background: Splicing factor 45 (SPF45) is an RNA splicing factor that binds to the single stranded 3'AG at the exon/intron border and promotes its utilization in the second catalytic step. SPF45 is involved in the regulation of alternative splicing and the utilization of cryptic splice sites. It has been shown to promote the utilization of a cryptic splice site created by the beta-110 mutation in the human beta-thalassemia gene. The resulting frameshift leads to sickle cell anemia [taken from the Universal Protein Resource (UniProt) Q96125].

    Gene ID

    84991

    NCBI Accession

    NP_116294

    UniProt

    Q96I25
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