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FRAS1 antibody (AA 1101-1200) (Biotin)

The Rabbit Polyclonal anti-FRAS1 antibody has been validated for ELISA, IHC (fro) and IHC (p). It is suitable to detect FRAS1 in samples from Human.
Catalog No. ABIN1700288

Quick Overview for FRAS1 antibody (AA 1101-1200) (Biotin) (ABIN1700288)

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 Biotin

Application

  • 13
  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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

    IHC-P 1:200-400
    IHC-F 1:100-500

    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 for 12 months.

    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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