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PQBP1 antibody (AA 150-200)

This anti-PQBP1 antibody is a Rabbit Polyclonal antibody detecting PQBP1 in WB, IP and IHC (fp). Suitable for Human and Mouse.
Catalog No. ABIN7454867

Quick Overview for PQBP1 antibody (AA 150-200) (ABIN7454867)

Target

See all PQBP1 Antibodies
PQBP1 (Polyglutamine Binding Protein 1 (PQBP1))

Reactivity

  • 35
  • 8
  • 7
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 1
Human, Mouse

Host

  • 33
  • 3
Rabbit

Clonality

  • 33
  • 3
Polyclonal

Conjugate

  • 18
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PQBP1 antibody is un-conjugated

Application

  • 30
  • 13
  • 13
  • 12
  • 8
  • 7
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 15
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 150-200

    Purpose

    Rabbit anti-PQBP1 Antibody, Affinity Purified

    Predicted Reactivity

    Bovine,Gorilla

    Purification

    Affinity Purified

    Immunogen

    between AA 150 and 200

    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: 2 - 5 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

    PQBP1 (Polyglutamine Binding Protein 1 (PQBP1))

    Alternative Name

    PQBP1

    Background

    Background: Polyglutamine-binding protein 1 (PQBP1) is a nuclear polyglutamine-binding protein that is involved with transcriptional activation. Mutations in the PQBP1 gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked mental retardation [taken from NCBI Entrez Gene (Gene ID: 10084].

    Gene ID

    10084

    NCBI Accession

    NP_005701

    UniProt

    O60828

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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