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UROD antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects UROD in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN629827

Quick Overview for UROD antibody (N-Term) (ABIN629827)

Target

See all UROD Antibodies
UROD (Uroporphyrinogen Decarboxylase (UROD))

Reactivity

  • 36
  • 10
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 32
  • 7
  • 1
Rabbit

Clonality

  • 36
  • 4
Polyclonal

Conjugate

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This UROD antibody is un-conjugated

Application

  • 34
  • 13
  • 13
  • 9
  • 8
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
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    N-Term

    Specificity

    UROD antibody was raised against the N terminal of UROD

    Purification

    Purified

    Immunogen

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

    WB: 2.5 µg/mL, IHC: 4-8 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    UROD Blocking Peptide, (ABIN5616924), is also available for use as a blocking control in assays to test for specificity of this UROD antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    UROD (Uroporphyrinogen Decarboxylase (UROD))

    Alternative Name

    UROD

    Background

    UROD is the fifth enzyme of the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.

    Molecular Weight

    40 kDa (MW of target protein)
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