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PRPF31 antibody (AA 449-499)

The Rabbit Polyclonal anti-PRPF31 antibody is suitable to detect PRPF31 in samples from Human. It has been validated for WB and IHC (fp).
Catalog No. ABIN7454569
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$457.43
$538.15
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Quick Overview for PRPF31 antibody (AA 449-499) (ABIN7454569)

Target

See all PRPF31 Antibodies
PRPF31 (Pre-mRNA Processing Factor 31 (PRPF31))

Reactivity

  • 56
  • 19
  • 13
  • 1
Human

Host

  • 48
  • 7
  • 2
Rabbit

Clonality

  • 32
  • 25
Polyclonal

Conjugate

  • 24
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This PRPF31 antibody is un-conjugated

Application

  • 49
  • 25
  • 18
  • 15
  • 12
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 9
    • 5
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 449-499

    Purpose

    Rabbit anti-PRPF31 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    Between AA 449 and 499

    Isotype

    IgG
  • Application Notes

    IHC: 1:500 - 1:2,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: Not recommended

    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

    PRPF31 (Pre-mRNA Processing Factor 31 (PRPF31))

    Alternative Name

    PRPF31

    Background

    Background: Pre-mRNA-processing factor 31 (PRPF31) is involved in pre-mRNA splicing and is required for U4/U6.U5 tri-snRNP formation. Defects in the PRPF31 gene are the cause of retinitis pigmentosa type 11 (RP11) [MIM:600138]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field [taken from the Universal Protein Resource (UniProt) Q8WWY3].

    Gene ID

    26121

    NCBI Accession

    NP_056444

    UniProt

    Q8WWY3

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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