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MVK antibody

The Rabbit Polyclonal anti-MVK antibody is suitable to detect MVK in samples from Human, Mouse and Rat. It has been validated for WB, ELISA and IHC.
Catalog No. ABIN7237444
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for MVK antibody (ABIN7237444)

Target

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

Reactivity

  • 54
  • 7
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 49
  • 5
Rabbit

Clonality

  • 40
  • 14
Polyclonal

Conjugate

  • 29
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This MVK antibody is un-conjugated

Application

  • 42
  • 16
  • 15
  • 11
  • 11
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human MVK

    Isotype

    IgG
  • Application Notes

    WB 1:200-1:1000, IHC 1:100-1:300

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.4 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    MVK (Mevalonate Kinase (MVK))

    Alternative Name

    MVK

    Background

    This gene encodes 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

    UniProt

    Q03426
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