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EML1 antibody (C-Term)

The Rabbit Polyclonal anti-EML1 antibody is suitable to detect EML1 in samples from Human, Mouse and Rat. It has been validated for WB.
Catalog No. ABIN632123
$1,297.32
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 9 to 12 Business Days

Quick Overview for EML1 antibody (C-Term) (ABIN632123)

Target

See all EML1 Antibodies
EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))

Reactivity

  • 9
  • 5
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 8
  • 1
Rabbit

Clonality

  • 8
  • 1
Polyclonal

Conjugate

  • 9
This EML1 antibody is un-conjugated

Application

  • 9
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 3
    • 1
    • 1
    • 1
    C-Term

    Specificity

    EML1 antibody was raised against the C terminal of EML1

    Purification

    Affinity purified

    Immunogen

    EML1 antibody was raised using the C terminal of EML1 corresponding to a region with amino acids YPCSQFRAPSHIYGGHSSHVTNVDFLCEDSHLISTGGKDTSIMQWRVI
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    EML1 Blocking Peptide, (ABIN936166), is also available for use as a blocking control in assays to test for specificity of this EML1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of EML1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))

    Alternative Name

    EML1

    Background

    Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type.

    Molecular Weight

    92 kDa (MW of target protein)
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