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FREM1 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects FREM1 in WB, IF and EIA. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN783634

Quick Overview for FREM1 antibody (C-Term) (ABIN783634)

Target

See all FREM1 Antibodies
FREM1 (FRAS1 Related Extracellular Matrix 1 (FREM1))

Reactivity

  • 10
  • 4
  • 1
Human, Mouse

Host

  • 10
Rabbit

Clonality

  • 10
Polyclonal

Conjugate

  • 7
  • 1
  • 1
  • 1
This FREM1 antibody is un-conjugated

Application

  • 6
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 4
    • 4
    • 1
    C-Term

    Specificity

    This antibody rescts with Muman and Mouse FREM1 and is predicted to not cross-react with other FRAS members.

    Purification

    Affinity Chromatography purified via peptide column

    Immunogen

    15 amino acid peptide near the carboxy terminus of Human FREM1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS, 0.02 % 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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    FREM1 (FRAS1 Related Extracellular Matrix 1 (FREM1))

    Alternative Name

    FREM1

    Background

    FREM1 is a member of the FRAS1-related extracellular matrix protein family and is thought to play a role in craniofacial and renal development. FREM1 functions as an extracellular matrix protein that is essential for epidermal adhesion during embryogenesis and may also participate in epidermal differentiation. It is recognized by cells in the embryonic skin and hair follicles through different members of the integrin family. Deficiency in the Fras1/Frem genes gives rise to the bleb phenotype, which is equivalent to the human hereditary disorder Fraser syndrome.Synonyms: C9orf143, C9orf145, C9orf154, FRAS1-related extracellular matrix protein 1, Protein QBRICK

    Gene ID

    158326

    NCBI Accession

    NP_001171175

    UniProt

    Q5H8C1
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