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FRAS1 antibody (AA 1101-1200) (AbBy Fluor® 488)

This Rabbit Polyclonal antibody specifically detects FRAS1 in IF (cc) and IF (p). It exhibits reactivity toward Human.
Catalog No. ABIN1694836

Quick Overview for FRAS1 antibody (AA 1101-1200) (AbBy Fluor® 488) (ABIN1694836)

Target

See all FRAS1 Antibodies
FRAS1 (Fraser Syndrome 1 (FRAS1))

Reactivity

  • 16
  • 1
  • 1
Human

Host

  • 16
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FRAS1 antibody is conjugated to AbBy Fluor® 488

Application

  • 12
  • 12
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

    • 14
    • 1
    AA 1101-1200

    Predicted Reactivity

    Human,Mouse,Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human FRAS1

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    FRAS1 (Fraser Syndrome 1 (FRAS1))

    Alternative Name

    FRAS1

    Background

    Synonyms: Extracellular matrix protein FRAS1, Fras 1, Fras1, FRAS1_HUMAN, Fraser syndrome 1.

    Background: This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].

    Gene ID

    80144

    UniProt

    Q86XX4
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