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MVK antibody (N-Term)

This anti-MVK antibody is a Rabbit Polyclonal antibody detecting MVK in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN631917

Quick Overview for MVK antibody (N-Term) (ABIN631917)

Target

See all MVK Antibodies
MVK (Mevalonate Kinase (MVK))

Reactivity

  • 45
  • 7
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 40
  • 5
Rabbit

Clonality

  • 41
  • 4
Polyclonal

Conjugate

  • 29
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MVK antibody is un-conjugated

Application

  • 33
  • 17
  • 12
  • 12
  • 6
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 10
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificity

    MVK antibody was raised against the N terminal of MVK

    Purification

    Affinity purified

    Immunogen

    MVK antibody was raised using the N terminal of MVK corresponding to a region with amino acids LAVLAFLYLYLSICRKQRALPSLDIVVWSELPPGAGLGSSAAYSVCLAAA
  • Application Notes

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

    Comment

    MVK Blocking Peptide, (ABIN940193), is also available for use as a blocking control in assays to test for specificity of this MVK antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of MVK 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

    MVK (Mevalonate Kinase (MVK))

    Alternative Name

    MVK

    Background

    MVK is the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash.

    Molecular Weight

    42 kDa (MW of target protein)
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