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PDZD9 antibody (AA 50-100) (AbBy Fluor® 350)

This anti-PDZD9 antibody is a Rabbit Polyclonal antibody detecting PDZD9 in WB and IF (p). Suitable for Human, Rat and Mouse.
Catalog No. ABIN1403763

Quick Overview for PDZD9 antibody (AA 50-100) (AbBy Fluor® 350) (ABIN1403763)

Target

See all PDZD9 Antibodies
PDZD9 (PDZ Domain Containing 9 (PDZD9))

Reactivity

  • 17
  • 15
  • 14
  • 2
  • 1
Human, Rat, Mouse

Host

  • 16
  • 1
Rabbit

Clonality

  • 17
Polyclonal

Conjugate

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PDZD9 antibody is conjugated to AbBy Fluor® 350

Application

  • 17
  • 12
  • 3
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

    • 14
    • 1
    • 1
    AA 50-100

    Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human PDZD9

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    PDZD9 (PDZ Domain Containing 9 (PDZD9))

    Alternative Name

    PDZD9

    Background

    Synonyms: PDZ domain containing 9, PDZ domain containing protein 9, PDZD 9, PDZK-9.\, PDZD9_HUMAN.

    Background: PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.

    Gene ID

    255762

    UniProt

    Q8IXQ8
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